Native American Research Centers for Health (NARCH) Grants, 78570-78586 [E8-30300]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Indian Health Service
Native American Research Centers for
Health (NARCH) Grants
Announcement Type: New and
Competing Continuations.
Funding Announcement Number:
HHS–2010–IHS–NARCHVI–0001.
Catalog of Federal Domestic
Assistance Numbers (s): 93.933.
Key Dates: Letter of Intent Deadline:
March 15, 2009.
Application Deadline Date: May 14,
2009.
Review Date: October, 2009.
Earliest Anticipated Start Date: June
1, 2010.
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I. Funding Opportunity Description
The Indian Health Service (IHS), in
conjunction with the National Institute
of General Medical Sciences (NIGMS)
and other institutes of the National
Institutes of Health (NIH) announces
competitive grant applications for
Native American Research Centers for
Health (NARCH), an initiative to
support new and/or continuing centers
or projects funded under the NARCH
grant program. This funding mechanism
will develop further opportunities for
conducting research and research
training to meet the needs of American
Indian/Alaska Native (AI/AN)
communities. This program is
authorized under the Snyder Act, 25
U.S.C. 13, the Public Health Service Act,
42 U.S.C. 241 as amended, and the
Indian Health Care Improvement Act, 25
U.S.C. 1602(a)(b)(16). This program is
described at 93.933 in the Catalog of
Federal Domestic Assistance.
Background Information:
The AI/AN Tribal nations and
communities have long experienced
health status worse than that of other
Americans. Although major gains in
reducing health disparities were made
during the last half of the twentieth
century, most gains stopped by the mid1980s (Trends in Indian Health 1998–
99) and a few diseases, e.g., diabetes,
worsened. ’’All Indian’’ rates contain
marked variation among the IHS Areas
or regions (Regional Differences in
Indian Health 1998–99); and variation
by Tribe exists within Areas as well.
The Trends and Regional Differences
reference can be found at the IHS Web
site at: https://www.ihs.gov/
NonMedicalPrograms/IHS_Stats.
Although the AI/AN mortality rates for
all cancers are about 20 percent lower
than the U.S. rates for all races, there is
variation among IHS Areas for specific
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cancers. Moreover, the favorable AI/AN
mortality rates for some cancers may be
due to markedly lower incidence rates
partly offset by higher case-fatality rates.
Unfamiliarity with modern health care
may adversely influence health status
among the elderly, the low-income
elderly, and Tribes, and also may reduce
the acceptability of health research
among them. The daunting tasks
confronting Tribes, researchers, and
health care and public health programs
in the beginning of the twenty-first
century are to resume the reduction of
health disparities that had occurred
through the 1980s, to reverse the
worsening in a few diseases, to maintain
and strengthen the favorable status, and
to reduce the disparities among and
within Areas and Tribes. Factors known
to contribute to health status and
disparities are complex, and include
underlying biology, physiology, and
genetics, as well as ethnicity, culture,
socioeconomic status, gender/sex, age,
geographical access to care, and levels
of insurance.
Additional factors known to
contribute to health status and
disparities include:
1. Family, home, and work
environments;
2. General or culturally specific health
practices;
3. Social support systems;
4. Lack of access to culturally
appropriate health care; and
5. Attitudes toward health.
Yet none of these alone, or in
combination, accounts for all
documented differences. Health
disparities of AI/ANs may also reflect a
lack of in-depth research relevant to
improving their health status. Many AI/
ANs distrust research for historical
reasons. One approach that combats this
distrust is to ensure that Tribes are the
managing partners in training and
research that involves them, as for
example, in community-based
participatory research (i.e., a
collaborative research process between
researchers and community
representatives). This approach is
especially helpful to design both
training relevant to researchers from
Tribal communities, and research
relevant to the health needs of the
communities.
Research Objectives:
The NARCH initiative will support
partnerships between Federally
recognized AI/AN Tribes or Tribal
organizations (including national and
area Indian health boards, and Tribal
colleges meeting the definition of a
Tribal organization as defined by 25
U.S.C. 1603(d) or (e)) and institutions
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that conduct intensive academic-level
biomedical, behavioral and health
services research. These partnerships
are called Native American Research
Centers for Health (NARCH). Due to the
complexity of factors contributing to the
health and disease of AI/ANs, and to
their health disparities compared with
other Americans, the collaborative
efforts of the agencies of the Department
of Health and Human Services (HHS)
and the collaboration of researchers and
AI/AN communities are needed to
achieve significant improvements in the
health status of AI/AN people. To
accomplish this goal, in addition to
objectives set by the Tribe, Tribal
organization or Indian health boards,
the IHS NARCH program will pursue
the following program objectives:
• To develop a cadre of AI/AN
scientists and health professionals—
Opportunities are needed to develop
more AI/AN scientists and health
professionals engaged in research, and
to conduct biomedical, clinical,
behavioral and health services research
that is responsive to the needs of the AI/
AN community and the goals of this
initiative. Faculty/researchers and
students at each proposed NARCH will
develop investigator-initiated,
scientifically meritorious research
projects, including pilot research
projects, and will be supported through
science education projects designed to
increase the numbers of, and to improve
the research skills of, AI/AN
investigators and investigators involved
with AI/ANs.
• To enhance partnerships and
reduce distrust of research by AI/AN
communities—Recent community-based
participatory research suggests that AI/
AN communities can work
collaboratively in partnership with
health researchers to further the
research needs of AI/ANs. Fully
utilizing all cultural and scientific
knowledge, strengths, and
competencies, such partnerships can
lead to better understanding of the
biological, genetic, behavioral,
psychological, cultural, social, and
economic factors either promoting or
hindering improved health status of AI/
ANs, and generate the development and
evaluation of interventions to improve
their health status. Community distrust
of research and researchers will be
reduced by offering the Tribe greater
control over the research process.
• To reduce health disparities—In the
Indian Health Care Improvement Act,
Public Law 94–437 (as amended), IHS
was legislatively mandated to improve
the delivery of effective health care to
AI/ANs. In the NIH Revitalization Act of
1993, NIH was encouraged to increase
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the number of under-represented
minorities participating in biomedical,
clinical, and behavioral research,
including studies on drug abuse and
alcoholism, and the examination of the
role of resiliency in the prevention and
treatment of those conditions. Also, the
‘‘Initiative to Eliminate Racial and
Ethnic Disparities in Health’’ by HHS
(https://www.omhrc.gov/rah) encouraged
NIH to help reduce health disparities. In
response to these priorities, the IHS and
NIH have established a collaboration to
support the NARCH.
Reducing health disparities among
AI/AN communities and individuals
may be fostered by greater
understanding of how to enhance their
strengths and resilience. While AI/AN
communities have relied on health
research and medical science to reduce
health disparities, they have also relied
on their own psychological,
organizational, and cultural assets and
strengths to survive major harms and
disruptions over the centuries, and to
rebound from insults to health.
The mission of NIH is to acquire new
knowledge that will lead to better health
by understanding the processes
underlying health and disease that in
turn will help prevent, detect, diagnose,
and treat disease and disability. The
NARCH initiative works toward the NIH
mission by supporting research that
discovers the interrelationships among
the many factors that contribute to
health and disease, and by helping to
train and promote AI/AN researchers
and researchers concerned with AI/AN
health.
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II. Award Information
Type of Awards: Grant.
Estimated Funds Available: The
estimated funds (total costs) available
for the first year of support for the entire
initiative is expected to be at least $2.0
million in Fiscal Year 2010. The actual
amount may vary, depending on the
response to the request for applications
(RFA) and availability of funds. An
applicant may request a project period
not to exceed four years of support, and
direct costs not to exceed $1,100,000 per
center or $550,000 per project (research
or training) in the first year of each
award. Direct costs to the applicant
include the total cost of each
subcontract (subcontractor direct plus
subcontractor indirect costs).
Anticipated Number of Awards: An
estimated five to fifteen awards will be
made under the program.
Award Amount: $100,000–$1,100,000
per year.
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III. Eligibility Information
The new or existing NARCH must be
a working partnership of the eligible AI/
AN organization and of the researchintensive institution. Applicants eligible
to receive the NARCH award are
Federally recognized Tribes and Tribal
organizations as defined under the
Indian Health Care Improvement Act, 25
U.S.C. 1603 (d) or (e), including eligible
Indian health boards or Tribal colleges
applying on behalf of eligible Federally
recognized Tribes or Tribal
organizations. As the grantee, the
eligible AI/AN organization will define
criteria and eligibility for participation
in all aspects of the partnership,
consistent with this announcement. A
minimum of 30 percent of the grant
funds must be budgeted in the
application to remain with the eligible
AI/AN organization(s); that is, no more
than 70 percent of the application’s total
budget may be contained in subcontract
budgets of the non-eligible
subcontracting partner institutions or
organizations.
1. Eligible Applicants—The AI/AN
applicant must be one of the following:
• A federally recognized AI/AN
Tribe, as defined under 25 U.S.C.
1603(d); or
• A Tribal organization, as defined
under 25 U.S.C. 1603(e), including
Tribal colleges or health boards meeting
this definition; or
• A consortium of two or more of
those Tribes or Tribal organizations.
Applicants other than Tribes must
provide proof of non-profit status.
2. Cost Sharing or Matching—The
NARCH program does not require
matching funds or cost sharing.
3. The Research-Intensive Partner—
The Research-Intensive Partner must be
an accredited public or private
nonprofit university, academic medical
center, or other institution that has an
established record of conducting
research into the health problems of AI/
AN; has demonstrated a commitment to
enhancing the capability of AI/AN
faculty/researchers, students,
investigators, and communities to
engage in biomedical, behavioral,
clinical and health services research;
and has demonstrated a commitment to
mentoring AI/AN faculty/researchers,
students, and investigators.
4. Principal Investigator—The
Principal Investigator, the individual
responsible for the administration
(including fiscal management) of the
overall project, must have his/her
primary appointment with the AI/AN
applicant organization. Special
arrangements of employment, such as
inter-organizational personnel
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agreements, are permissible. The
Principal Investigator may be, but is not
required to be, the NARCH Program
Director or a Research Project
Investigator. The NARCH Principal
Investigator may or may not have formal
academic/research credentials, but if
not, then the NARCH Program Director
must be so qualified.
The traditional NIH research project
grant consists of a single Principal
Investigator (PI) working with a small
group of subordinates on an
independent research project. Although
this model clearly continues to work
well and encourages creativity and
productivity, it does not always work
well for multidisciplinary efforts and
collaboration. Increasingly, healthrelated research involves teams that
vary in terms of size, hierarchy, location
of participants, goals, disciplines, and
structure. There is growing consensus
that team science would be encouraged
if more than one PI could be recognized
on individual awards. The NIH has
adopted a multiple-PI model, as recently
directed by the Office of Science and
Technology Policy. All agencies that
have research and research-related
programs must offer the multiple-PI
model as an option. Note, it is only an
option, not a requirement. The
traditional NARCH division of roles
between PI and Project Director will
usually address these issues to a
satisfactory degree. For additional
information regarding the new multiplePI model, please click on the following
website: https://grants.nih.gov/grants/
multi_pi/index.htm.
5. NARCH Program Director—The
NARCH Program Director is the
individual responsible for the day-today leadership and management of the
research and training programs within
the proposed NARCH. The Program
Director may be, but is not required to
be, the Student and Faculty/Researcher
Development Director or a Research
Project Investigator. The NARCH
Program Director may or may not have
formal academic/research credentials,
but if not, then the Principal
Investigator must be so qualified.
6. Student and Faculty/Researcher
Development Director and Participant—
The NARCH initiative is an institutional
developmental grant mechanism that
places an emphasis on the continual
development of students and faculty/
researchers. If a new Student and/or
Faculty/Researcher Development
Program is proposed in the current
application, then the Principal
Investigator of that project is expected to
be the NARCH Student and Faculty
Development Director. In order to be
included as the Student and Faculty
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Development Director, the prospective
director must have a faculty/researcher
appointment at the research-intensive
institution (or equivalent appointment
at the AI/AN organization or other
consortium partner) and must
demonstrate that he/she has the
knowledge, skills, and capabilities to
mentor students and faculty/researchers
and to generate and direct development
and mentoring programs.
The Student and Faculty
Development Director may be the
NARCH Program Director. Faculty/
researchers and students should be
supported in research education
activities that improve their skills and
abilities to be successful at the next
stage of their professional development.
To be included as a participant for
faculty/researcher development in the
proposed NARCH, the individual must
have a faculty/researcher appointment
at the research-intensive institution or
equivalent appointment at the AI/AN
organization or consortium partner.
7. Research Project Investigators—The
NARCH initiative is an institutional
developmental grant mechanism that
places an emphasis on continual
improvement of the research
competitiveness of the research
investigators. In order to be included as
a research project investigator in the
NARCH, a prospective investigator must
have a faculty appointment at the
research-intensive institution or
equivalent appointment at the AI/AN
organization or other consortium
partner, and must show that he/she has
the need, based on institutional,
departmental, and professional
development plans, to enhance his/her
research knowledge, skills, and
capabilities by engaging in the proposed
research program and associated
activities.
8. Tribal Approval of the
Application—It is the policy of the IHS
that all research involving AI/AN Tribes
be approved by the Tribal governments
with jurisdiction. Therefore, the
following documentation is required as
part of the application for new or
continuing centers or additional
NARCH projects:
• Tribal Resolution:
If the applicant is an Indian Tribe or
Tribal organization, a resolution
supporting the project from the Tribal
government of all Tribes to be served
must accompany the application
submission. Applications by Tribal
organizations will not require
resolutions if the current Tribal
resolutions under which they operate
would encompass the proposed
activities. In this instance, a copy of the
current resolution must accompany the
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application. The listed Tribes to be
served by the project in the proposal
must match the set of appended
resolutions. If a resolution from an
appropriate representative of each Tribe
to be served is not submitted prior to
October 1, 2009, the application will be
considered incomplete and will not be
considered for funding.
An official signed resolution must be
received by October 1, 2009 by the
Division of Grants Operations (DGO),
IHS, at the Reyes Building, 801
Thompson Avenue, TMP 360, Rockville,
MD 20852. A grant will not be awarded
unless the signed resolution is received.
Please include the funding opportunity
number, as a reference to this
announcement, if the resolutions are
submitted as a separate mailing.
9. Mechanism of Support—Awards
under this initiative will be
administered using the competing
institutional grant mechanism of the
IHS, and will be reviewed using the NIH
S06 mechanism.
IV. Application and Submission
Information
1. Address to Request Application
Package: NARCH Program Official,
Reyes Building, 801 Thompson Avenue,
Rockville, MD 20852 or by e-mail to
narch@ihs.gov. Applicants are strongly
encouraged to establish eligibility of
their proposed applications prior to
submission. Inquiries about eligibility
should be addressed to Alan
Trachtenberg, M.D., M.P.H., at (301)
443–0578 or by e-mail to narch@ihs.gov.
The application package, including
supplemental instructions will be
posted on the IHS Research Program
Web site, at: https://www.ihs.gov/
MedicalPrograms/Research/narch.cfm.
Technical assistance will be made
available for applicants, and first time
applicants are urged to take advantage
of it. To sign up for technical assistance,
potential applicants should e-mail their
contact information to narch@ihs.gov
with the words ‘‘technical assistance’’ in
the subject heading and full contact
information, including email address,
listed in the body of the e-mail.
The NIH instructions for the PHS 398
application form are available in an
interactive format at: https://
grants.nih.gov/grants/funding/phs398/
phs398.html. Applicants must use the
currently approved version of the PHS
398. For further assistance contact
GrantsInfo, Telephone (301) 435–0714,
e-mail: GrantsInfo@nih.gov,
Telecommunications for the hearing
impaired: TTY 301–451–0088.
Submit a typed and signed original
application, including the Checklist,
and one (1) single-sided photocopy of
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the entire application (including
Appendices and supporting documents)
in one package to: Division of Grants
Operations, Indian Health Service,
Reyes Building, 801 Thompson Avenue,
TMP 360, Rockville, MD 20852–1627
(zip code is unchanged for express/
courier services), Telephone: (301) 443–
5204.
‘‘Native American Research Centers
for Health’’ and the RFA number NOTGM–09–010 must be typed on line 2 of
the face page of the application form
and the YES box must be marked.
At the time of submission, applicants
must also send four (4) additional
single-sided photocopied and signed
applications, including the Checklist,
Appendices, and supporting
documentation to: Center for Scientific
Review (CSR), National Institutes of
Health, 6701 Rockledge Drive, Room
6160—MSC 7892, Bethesda, MD 20892–
7720, Bethesda, MD 20817 (for express
or courier service). Telephone: (301)
435–0715. The CSR no longer accepts
hand delivered applications. E-mail or
other electronic applications will not be
accepted under this announcement.
Specific supplementary instructions
for the PHS 398 application and budget
preparation for the NARCH program
may be obtained from the initiative
contacts listed under VII. Agency
Contacts, and will be posted at: https://
www.ihs.gov/MedicalPrograms/
Research/narch.cfm. They will also be
sent to any potential applicant who emailed their contact information to
narch@ihs.gov with the words
‘‘technical assistance’’ in the subject
heading.
There will be no acknowledgment of
receipt of the application.
2. Content and Form of Application
Submission:
A proposed NARCH may include any
or all of the following components:
Student development projects; faculty/
researcher development projects;
research projects (including pilot
projects); and ‘‘core’’ administrative
facilities.
The content of the application should
explain the components of the
application, and how they help meet the
purposes of the NARCH initiative. A
description should be provided of the
current state of the research and
research training enterprise at the
proposed NARCH and its institutional
and community partners, including
faculty/researcher and student profiles.
A clear statement should be presented
of the overall goals, specific measurable
objectives, and anticipated milestones.
These elements should be presented in
the context of needed improvements in
the partners’ organizational
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infrastructure and environment for
research. Documentation should be
provided to establish that the researchintensive partner is an institution with
a record of conducting research into the
health of AI/ANs, and that it has a
demonstrated commitment to the
special encouragement of, and
assistance to, AI/AN faculty/researchers,
students, investigators, and
communities for enhancing their
capacity to engage in biomedical,
behavioral and health services research.
For competitive renewals of existing
NARCH grants, previous
accomplishments and progress from the
time of the initial NARCH award must
be described. Documentation about the
nature of the partnership itself should
be included, such as: the process to
develop the application and proposed
NARCH itself, the past and future efforts
to increase the capacity of the partners
to improve their partnership, and efforts
to contribute to the success of the
NARCH. Applicants are encouraged to
articulate plans for the development of
partnerships toward the possible
planning of a national native health
research conference or other national
research training. The development of
additional future collaborative research
and research training opportunities
should also be an integral part of each
NARCH core proposal. For previously
existing NARCH centers, a specific and
detailed list of accomplishments and
assessment of the benefits from the
previous NARCH grant(s) is required.
A plan for assessment of the benefits
of the activities by the proposed NARCH
on specific, measurable outcomes
identified in the application should be
provided. IHS and NIGMS recognize
that Tribes, Tribally-based
organizations, and research-intensive
institutions are diverse in their
missions, their health and economic
status, and their cultures. Such an
assessment for a new NARCH could
include a self-study by the proposed
NARCH and its partners, which focuses
on fact-finding, program evaluation, and
recommendations for improvement in
key areas.
Strategies for determining the initial
and ongoing success of their efforts for
organizational development should also
be presented. It is expected that each
proposed NARCH will develop its own
set of strategies that best match its
circumstances. Guidance and
suggestions for program evaluation of a
proposed NARCH can be obtained from
https://www.the-aps.org/education/
promote/promote.html. For applications
that are competing renewals of existing
NARCH centers, the report and
evaluation of the progress made under
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the previous NARCH grant(s) will be a
key part of the application.
Applicants are strongly urged to
contact NARCH initiative staff at an
early stage to request the specific
supplementary instructions for the PHS
398 for the NARCH grants.
Supplementary instructions may be
obtained from the initiative contacts
listed under VII. Agency Contacts, and
will be posted at: https://www.ihs.gov/
MedicalPrograms/Research/narch.cfm.
They will also be sent to any potential
applicant who e-mailed their contact
information to narch@ihs.gov with the
words ‘‘technical assistance’’ in the
subject heading.
If Student Development Projects are
proposed, the NARCH application
should describe new programs or
modifications or additions to existing
programs of the partners that encourage
and facilitate AI/AN students to enter,
advance, and remain in health research
careers. Such projects might include,
but are not limited to, providing
employment as research assistants in
research projects of research-active
mentors with an explicit mentoring
plan, providing other mentoring with an
explicit mentoring plan, providing
workshops to improve technical or
communication skills, providing
motivating seminars or journal clubs
highlighting problems of interest to
students, providing contact with role
models, and providing opportunities to
travel to present results at national
scientific meetings. If research
mentorships or apprenticeships are
proposed, the application should clearly
document the experience, proposed
commitment, and quality of the mentors
in providing guidance and advice to
students (including responsible conduct
of research and research integrity,
teaching, and protection of human
subjects), and in fostering the
development of academic and/or
community-based AI/AN researchers.
The application should describe how
the development plans for the students
will meet both the individuals’
professional development goals, and
one purpose of the NARCH initiative:
To develop a cadre of AI/AN scientists
and health professionals. The
application must have an evaluation
plan for the new project(s) that indicates
the anticipated outcomes relative to the
current baseline data. For example, one
outcome might be the improved
retention of AI/AN students in science
majors. The application should indicate
the anticipated (quantitative)
improvement relative to the current
retention rate. Accomplishments of (and
connections with) any previously
funded NARCH student development
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projects by the applicant or partners
must be described.
A student in a NARCH Student
Development Project must be a full-time
or part-time student officially enrolled
in an educational program leading to an
undergraduate or graduate degree, or in
a post-doctoral educational program, or
(if well justified) in late high school. A
helpful book about mentoring science
students is found at https://
books.nap.edu/catalog/5789.html.
If Faculty/Researcher Development
Projects are proposed, the NARCH
application should describe the need,
proposed activity, and anticipated
outcomes. Faculty/researcher
development projects might include, but
are not limited to, short-term mentored
research experiences in the lab of an
active NIH-extramurally-funded
researcher with an explicit mentoring
plan, long-term general mentoring under
an explicit mentoring plan, or
attendance at workshops or courses or
national meetings needed for acquiring
specific skills or methodologies needed
for prospective research. As with
student development projects, the
application should document the
experience, proposed commitment, and
quality of the mentors, teachers, or
experience in providing guidance and
advice to faculty/researchers, and in
fostering the development of academic
and community-based AI/AN research.
The application must also describe the
evaluation plan for the faculty/
researcher development project. The
application must clearly describe how
the development plans for faculty/
researchers will meet both the
individuals’ professional development
goals, and two purposes of the NARCH
initiative:
• To develop a cadre of AI/AN
scientists and health professionals, and
• To enhance the partnership of the
proposed NARCH.
For grantees with previous NARCH
funding for faculty/researcher
development projects, a detailed list of
the accomplishments of (and
connections with) any previously
funded NARCH faculty/researcher
development projects by the applicant
or partners must be described.
NARCH applications may include a
maximum of five (5) regular Research
Projects and a maximum of five (5) Pilot
Research Projects. Unlike regular
research projects, a pilot research
project is limited in scope and is not
expected to have preliminary data. It is
also limited to a budget of no more than
$75,000 direct costs per year for four
years. The pilot research project is
intended for faculty/researchers without
current Federal research support.
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Support for faculty/researchers
participating in pilot research projects is
preparatory to seeking more substantial
funding from NIH research grant
programs (e.g., Academic Research
Enhancement Award, K, and R01
awards), as well as funding from other
agencies and private sources. Funds
received from the proposed NARCH to
support pilot research projects may not
be used to supplement ongoing research
projects. A NARCH application need not
include both research projects and pilot
research projects. Applications for only
pilot research projects or for only
research projects may be submitted.
Individual project investigators may
propose either a research project or a
pilot research project, but not both. For
research projects that are continuations
or modifications or outgrowths of
research projects (including pilot
research projects) under previous
NARCH grants, the accomplishments of
the previous research project(s) should
be detailed and a logical description
given as to how the results of the
previous work has led to the current
proposal.
Each research project or pilot research
project should follow the instructions
provided in PHS 398 (Revised 11/2007)
for preparing research grant
applications. The professional
development goals must clearly describe
specific objectives and milestones
which should include, but are not
limited to, improving competitiveness
in acquiring grant support. The
applicant should describe how
successful completion of the proposed
research project will improve the
research skills and will help develop the
students and faculty/researchers, thus
contributing to the overall goals and
specific measurable objectives of the
proposed NARCH.
Each research project or pilot research
project must follow the IHS policy
concerning Tribal approval, that all
research involving AI/AN Tribes be
approved by the Tribal governments
with jurisdiction. That is, each grantee
must include a resolution of approval
from the Tribal government(s), or (if
applicable) a letter of support signed by
the Executive Director or CEO of the
eligible AI/AN organization, or both (if
applicable) for projects that involve
people or community(ies) of an AI/AN
Tribe, or an eligible Tribal organization.
For NARCH proposals from multi-Tribal
consortia with projects that involve only
one or a few of the Tribes of the
consortium, some description should be
provided as to the process through
which the particular Tribes were chosen
to participate.
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Research projects (including pilot
research projects) proposed under this
initiative must be in research areas
normally funded by any of the NIH or
other research agencies in the HHS.
Research projects addressing health
disparities and the health priorities of
the AI/AN partner are especially
encouraged.
A listing of grants recently funded by
NIH may be found at Computer
Retrieval of Information on Scientific
Projects (CRISP), a searchable database
of Federally-funded biomedical research
projects conducted at universities,
hospitals, and other research
institutions. It may be accessed at
https://report.nih.gov/crisp/
crispquery.aspx. The following
agencies, institutes, offices, and centers
have stated particular interests in
supporting research under the NARCH
Program as follows:
National Institute of Dental and
Craniofacial Research (NIDCR)
Oral Health Research
NIDCR is committed to reducing the
disproportionate burden of oral diseases
experienced by AI/ANs. The focus of
NIDCR’s health disparities research is
on improving oral health status and
quality of life by understanding and
addressing oral diseases that are
prevalent in AI/AN communities,
specifically caries (including early
childhood caries), oral and pharyngeal
cancer, and periodontal disease.
Interdisciplinary research teams and the
full participation of communities are
viewed by NIDCR as essential
components of any health disparities
research.
Data that document oral disease
prevalence are readily available for
some populations, but not for others.
Homogeneity in subgroups of
populations cannot be assumed. For
instance, there are national data for
Mexican Americans, but not for the
numerous other Hispanic subgroups.
Similarly, data regarding the oral health
status of various AI/AN Tribes are
unavailable. Moreover, available data
provide little insight into the etiology or
determinants of oral disease and oral
health. The paucity of quality data and
conceptual models concerning the broad
array of potential determinants and riskfactors inhibits progress toward
preventing disease, and improving oral
health status and quality of life. The
NIDCR invites applications that, in
preparation for intervention research,
explore the complex array of social,
behavioral, psychological, contextual,
environmental, and biological factors
and their interactions that may
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contribute to oral health disparities
within AI/AN communities. Including
oral health status measures within
broader epidemiologic studies is
encouraged. However, applications that
are limited to the assessment of disease
prevalence and that explore a very
limited range of potential determinants
will be considered non-responsive.
The NIDCR has particular interest in
intervention research that will provide
clinically meaningful outcomes and
essential information needed to inform
clinical practice, public health policy,
health care provision, community and/
or individual action. Intervention
studies that are grounded in theory are
needed. Both basic and applied
intervention research applications are
invited. Studies may need to intervene
at multiple levels within communities.
The NIDCR encourages the use of the
strongest research design possible and
recognizes that not all intervention
research is amenable to randomized
clinical trials. Examples of health
disparities intervention research of
interest to the NIDCR includes but are
not limited to:
• Effectiveness studies that tailor/
target preventive approaches to
communities/individuals;
• Research that intervenes in novel
ways on macro- or intermediate level
determinants of oral health status;
• Health services research that
explores alternative approaches to
delivering preventive oral health care;
• Studies that intervene on common
risk factors or that take a systems
approach;
• Studies that explore multifaceted
strategies to intervene at several levels
within society;
• Dissemination and implementation
research at multiple organizational
levels; and
• Research that uses appropriate
technology for translation,
implementation, adoption, adherence,
and acceptance of oral disease
prevention programs in defined
populations, clinics, and communities.
Intervention research should be
reasonably applicable to a specific AI/
AN population. To facilitate adequate
enrollment and generalizability,
intervention studies may need to be
conducted at multiple sites. Studies
may be conducted at a single site only
if enrollment is adequate and if
sufficient numbers of participants are
available to allow extrapolation of
clinically meaningful results to the
specific AI/AN population of
interest.Pilot research projects that are
designed to lead to larger research
projects funded as part of a center or as
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free-standing NIH grants may be
proposed.
For additional information about oral
health research contact: Ruth NowjackRaymer, M.P.H., PhD, Director, Health
Disparities Research Program, National
Institute of Dental and Craniofacial
Research, 6701 Democracy Blvd., Room
640, Bethesda, MD 20892–4878, Phone:
(301) 594–5394, Fax: (301) 480–8322, email: nowjackr@mail.nih.gov.
National Institute on Drug Abuse
(NIDA)
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Neuroscience and Drug Abuse Research:
AI/ANs demonstrate higher rates of
drug abuse, particularly
methamphetamine, tobacco and alcohol
abuse, relative to other racial subgroups.
According to 2002–2006 National
Survey on Drug Use and Health
(NSDUH) data, AI/AN past year
methamphetamine use was 1.4%
compared to 0.1% for African
Americans, 0.6% for Hispanics or
Latinos and 0.7% for Whites. Prevalence
of use is high in both men and women.
Drug abuse patterns among AI/AN are
complex and can vary by factors such as
Tribe and geographic location. While
some datasets are available that can
provide general epidemiological data
regarding use and abuse rates in this
group, data are needed that better clarify
where use rates are highest, among
which Tribes, age and gender groups
and the factors that predict drug abuse
in these locales and groups. These data
will assist in developing more targeted
interventions and in identifying
mechanisms related to drug abuse
which can then serve as focal points for
intervention.
In addition to scarce data on patterns
of use, limited data are available
assessing drug abuse prevention and
treatment interventions for AI/AN. The
matrix model has been proposed in
particular to address methamphetamine
abuse, but few data are available to
assess the efficacy of this approach with
this population. Several preventive
interventions have been designed
particularly for this population and
results from them indicate their value,
but more research is needed to clarify
why these sometimes don’t work in
expected ways and whether the
interventions that are being used but
have not been evaluated are working to
reduce drug use.
The NIDA is committed to reducing
health disparities in drug abuse and
related health and social consequences
among AI/AN. Further, the Institute
supports methodologies required by the
NARCH, expecting that studies be
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developed and implemented using
community participatory approaches.
Research topics of interest include but
are not limited to:
• Studies that explore a range of
behavioral, cultural, environmental, and
individual factors that contribute to
drug abuse;
• Studies that explore the
consequences of drug abuse among AI/
ANs;
• Studies that consider the full
context of drug abuse, including
poverty, family factors, school factors,
intergenerational trauma, etc.;
• Studies that explore the role of
traditional practices and spirituality in
protecting against drug abuse;
• Studies that explore other factors
that protect against use in those groups
for whom use rates are lower;
• Studies that explore the efficacy
and/or effectiveness of culturally
relevant preventive interventions;
• Studies that explore the efficacy
and/or effectiveness of culturally
relevant treatment interventions;
• Studies that assess factors related to
service utilization, including use rates
and access to services, either in
reservation or urban settings; and
• Studies that explore the
organization, management and delivery
of interventions.
For additional information about
neuroscience or drug abuse research
contact: Kathy Etz, PhD, National
Institute on Drug Abuse, 6001 Executive
Blvd., Room 5153 MSC 9589, Bethesda,
MD 20852, Phone: (301) 402–1749, Fax:
(301) 480–2543, e-mail:
Kathleen.Etz@nih.hhs.gov.
National Institute on Alcohol Abuse and
Alcoholism (NIAAA)
Alcohol Research
NIAAA is committed to reducing the
disproportionately high burden of
illness associated with alcohol use,
abuse, and dependence among AI/AN
people. Alcohol-associated disabilityadjusted life years (DALYs) remain
highest among AI/ANs in comparison to
all other U.S. ethnic groups. AI/AN
people suffer from unacceptably high
rates of alcohol abuse and dependence,
alcohol-related morbidity and mortality,
and intentional and unintentional
injuries associated with alcohol use.
Nevertheless, AI/AN people are
heterogeneous on many dimensions
with over 562 Federally-recognized
Tribal entities. To address alcoholrelated health disparities of AI/AN
people, more needs to be known about
how differences between Tribes,
geographic regions, residence on
reservations, urban or rural areas, as
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well as more typical demographic
variables such as age, education,
income, and gender influence alcohol
use and associated health status
outcomes. Such information can guide
the development of more effective and
culturally appropriate ways of
identifying and intervening with those
who suffer from alcohol-related
problems, as well as preventing alcohol
problems before they occur. Additional
research is also needed to understand
how to best advance the dissemination
of research findings on alcohol and
health, so that AI/AN people can benefit
from the latest research discoveries.
Finally, NIAAA is aware that oftentimes
researchers who conduct investigations
among communities of color are
members of these cultural, racial or
ethnic groups themselves. NIAAA is
committed to identifying and providing
training and mentoring experiences to
help AI/AN alcohol researchers advance
the science of alcohol use and give back
to their communities.
The NIAAA is committed to reducing
alcohol related health disparities and is
committed to the NARCH program.
Research topics of interest to NIAAA
include but are not limited to:
—Studies that assess the differing needs
of various Tribal groups, considering
variations in rates of alcohol use,
misuse and abstinence.
—Studies that develop new
interventions or adapt existing
prevention and/or treatment
interventions that take strengths of the
AI/AN culture into consideration.
—Studies that investigate the
application/adaptation of evidence
based interventions among AI/AN
groups.
—Studies that investigate how
traditional spiritual and medical
treatments can be applied/adapted to
improve intervention outcomes
among AI/AN peoples.
—Studies that explore the effectiveness
and/or efficacy of commonly used
interventions such as screening and
brief intervention or referral among
AI/AN populations.
—Studies that investigate the risk and
protective factors associated with
drinking among women of
childbearing age so as to inform
culturally sensitive, effective FASD
prevention.
—Studies that investigate ways to delay
onset of youth drinking among AI/AN
young people.
—Studies that investigate the
association between alcohol use and
suicide among AI/AN people,
especially youth. Studies may attempt
to understand the individual and
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group level variables that contribute
to ‘‘epidemics’’ of suicide among AI/
AN youth.
—Studies that explore the consequences
of alcohol use and misuse among AI/
AN peoples; these consequences may
include but are not limited to other
social and health problems (i.e.,
diabetes, obesity, poor nutrition,
cancer, liver disease, etc.),
interfamilial violence, intentional and
unintentional injury, and driving
under the influence.
—Studies that investigate the
acceptance and efficacy of
pharmacotherapy for alcohol abuse
and dependence within integrated
health counseling approaches.
—Studies that investigate the influence
of alcohol use on the spread and
treatment of Human
Immunodeficiency Virus (HIV)/
Acquired Immune Deficiency
Syndrome (AIDS) among AI/AN
peoples.
For additional information contact:
Judith A. Arroyo, PhD, Minority
Health and Health Disparities
Coordinator, Project Official, Division of
Epidemiology and Prevention Research,
National Institute on Alcohol Abuse and
Alcoholism, 5635 Fishers Lane Room
2079, Bethesda, MD 20892–9304, (for
Fed Ex use Rockville, MD 20852–1705),
Office: 301–402–0717, Fax: 301–443–
8614, e-mail:
Judith.Arroyo@nih.hhs.gov.
National Cancer Institute (NCI)
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Cancer Health Disparities Research
The Center to Reduce Cancer Health
Disparities (CRCHD) is committed to
reducing cancer health disparities
among AI/ANs. Investigators are
encouraged to submit research projects
addressing every aspect of cancer and
cancer health disparities research.
CRCHD welcomes investigations in
basic, clinical, translational, and
population-based research addressing
cancer health disparities among AI/AN.
The CRCHD is central to the NCI’s
efforts to reduce the unequal burden of
cancer in our society. As part of these
efforts, the Diversity Training Branch,
CRCHD, has been supporting NARCH
projects with cancer relevance since
2003.
For additional information contact:
Dr. Peter Ogunbiyi, Program Director,
Diversity Training Branch, Center to
Reduce Cancer Health Disparities,
National Cancer Institute, 6116
Executive Boulevard, Suite 602,
Bethesda, MD 20892–8341 (U.S. Postal
Service), Phone: 301–496–7344, Fax:
301–435–9225, e-mail: po43t@nih.gov.
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Health Literacy Research:
The HHS, in its Healthy People 2010
initiative, defines health literacy as,
‘‘the degree to which individuals have
the capacity to obtain, process, and
understand basic health information
and services needed to make
appropriate health decisions.’’ (Please
see: https://www.healthypeople.gov/
document/HTML/Volume1/
11HealthCom.htm). Health literacy is a
complex phenomenon that involves
individuals, families, communities, and
systems. For instance, consumers,
patients, caregivers, traditional healers,
or other laypersons may vary with
respect to:
• Access (e.g., to audienceappropriate information, media or
professionals);
• Skills (e.g., to gather and
comprehend health information; to
speak and share personal information
about health history and symptoms; to
act on information by initiating
appropriate follow-up visits and
conveying understanding back to the
information source; to make decisions
about basic healthy behaviors, such as
healthy eating and exercise; to engage in
self-care and chronic disease
management);
• Knowledge (e.g., of health and
medical vocabulary, concepts such as
‘‘risk’’, the organization and functioning
of healthcare systems, cultural beliefs
and possible differences in traditional
and current medical systems about
disease causation, prevention and
treatment);
• Abilities (e.g., sensory,
communication, cognitive, or physical
challenges or limitations);
• Features of health care providers
and public health systems (e.g., the
communication skills of health
professionals, platforms employed for
patient education, built environments,
and signage);
• Traditional healers and their role,
especially in relation to the existing
medical systems which could lead to
different understanding in health and
disease progression;
• Demographics (e.g., developmental
or life stage, cultural, linguistic, or
educational differences that affect
health beliefs, knowledge, and
communication).
Too often people with the greatest
health burdens have limited access to
relevant health information. One reason
is the complex and cumbersome ways in
which health information is presented.
Health care professionals may not
communicate effectively with
individuals. For instance, achieving
informed consent for treatment is
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difficult when health care personnel
cannot explain biological processes or
treatment procedures in simplified
language and patients cannot interpret
health information. These situations
hamper the effectiveness of health
professionals’ efforts to prevent,
diagnose, and treat medical conditions,
and limit many health care consumers’
abilities to make important health care
decisions. Another reason is due to
individuals’ limited abilities to fully
interpret and understand complex
health terminology and instructions.
This could be further exacerbated by
different belief systems and adoption of
methods for prevention and treatment.
Limited numeracy can also impede the
ability to make personal decisions
related to risk, risk avoidance, and risk
reduction. For instance, to follow health
care instructions, patients need to be
able to comprehend written and oral
prescription instructions, directions for
self-care, and plans for follow-up tests
and appointments.
Specific Objectives
Researchers are strongly encouraged
to review the general illustrative
examples of topics relevant to health
literacy provided below. Applications
should address health promotion,
prevention, treatment, or management
of diseases or health conditions, and/or
the improvement of health or health
care outcomes. The research must
involve at least one of the following:
• Health literacy, or one of its many
components, as a key outcome;
• Health literacy as a key explanatory
variable for some other outcome;
• Methodological or technological
improvement to strengthen research on
health literacy; and/or
• Prevention and/or intervention
strategies that focus on health-literacy.
Studies to develop, or evaluate, the
readability or utility of specific
materials that are intended for single
uses or single audiences are not
responsive to this program
announcement unless these
investigations are integral to testing a
significant research hypothesis related
to health literacy.
Approaches
A wide variety of research approaches
are encouraged:
• Basic research that investigates or
describes the nature of health literacy
and the magnitude of health literacy
problems;
• Applied research addressing issues
pertinent to health literacy practices
(e.g., systems level interventions) and
research-in-practice (e.g., active
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potential end users participate as
supportive research partners);
• Develop theoretical models, refine
research constructs, improve methods
and measurements, and establish causal
relationships (e.g., between low health
literacy and lack of effective health
promotion);
• Evaluation research that develops
and tests the effectiveness of
interventions, or adapts and tests
existing programs (including those that
are implemented by health care systems
and systems outside of health care), to
reduce low health literacy and its
adverse consequences;
• Secondary analyses of existing
datasets as well as meta-analytic
studies; and
• Multilevel, multidisciplinary,
interdisciplinary, and transdisciplinary
research is encouraged, especially
studies that incorporate individual,
family, community and societal
mediators of health literacy in
childhood and adulthood, or state-ofthe-art health communication theory
and knowledge.
For additional information about NCI
health literacy research contact: Sabra F.
Woolley, Ph.D., Program Director,
Health Communication and Informatics
Research Branch, National Cancer
Institute, 6130 Executive Blvd. Room
4084, Bethesda, Maryland 20892–7365,
Phone: 301–435–4589, Fax: 301–480–
2087, E-mail:
Sabra.Woolley@nih.hhs.gov.
Tobacco Control Research
AI/ANs have been documented to
have the highest smoking rate of any
major racial/ethnic group in the U.S.
According to the 2005 National Health
Interview Survey of adults 18 and over,
32% of AI/AN are current smokers,
compared with 21.9% of non-Hispanic
whites, 21.5% of non-Hispanic blacks,
13.3% of Asians and 16.2% of
Hispanics. Prevalence of smoking is
high among both men (37.5%) and
women (26.8%).(1) A similar pattern can
be seen among youth, where AI/AN
youth have substantially higher smoking
prevalence (23.1%) than non-Hispanic
whites (14.9%), Hispanics (9.3%), nonHispanic blacks (6.5%), and Asians
(4.3%), according to data from the
National Survey on Drug Use and
Health. These data also show that nonsmoking AI/AN youth demonstrated
higher susceptibility to experimenting
with smoking than most other racial/
ethnic groups.(2)
At the same time, however, tobacco
use patterns among the AI/AN
population are complex and can vary
substantially among subgroups of this
population. Smoking rates among AI/
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ANs vary widely by region, being
highest in the northwestern United
States, in Canada, and in Alaska.
Additionally, use of smokeless tobacco
is higher among AI/AN adults compared
with other racial/ethnic groups. Some
studies have found particularly high
rates of smokeless tobacco use (greater
than 50%) among AN populations,
including pregnant women, due to the
use of Iqmik, a traditional form of
smokeless tobacco.(3)
Understanding tobacco use among
Native American populations is also
complicated by the fact that tobacco has
had a substantial role in Native
American culture and tradition.
Historically, tobacco has been used in
medicinal and healing rituals and in
ceremonial and religious practices. It is
important to distinguish the traditional,
ceremonial uses of tobacco, which are
limited to specific occasions, from
addictive use of tobacco products.
However, the relationship between
these different contexts of tobacco use
and their impact on behavior has not
received sufficient scientific study.
Moreover, limited data are available
on the effectiveness of tobacco use
cessation interventions targeted to AI/
ANs. Preliminary focus group studies
suggest that Native American smokers
are more likely to have negative
attitudes towards pharmacotherapies,
such as concerns about side effects and
lack of trust in conventional
medicine.(4) Thus, there is a need to
develop culturally-appropriate
interventions targeted to this
population.
The NCI Tobacco Control Research
Branch is committed to supporting
transdisciplinary research aimed at
reducing disparities in tobacco use and
related health outcomes. The NARCH
provides a unique mechanism to
support collaborative research involving
researchers from multiple disciplines to
address a complex scientific and public
health challenge.
Sample research areas of interest
include but are not limited to the
following:
• Studies to understand the role of a
range of behavioral, cultural, and
environmental factors that lead to
initiation of tobacco use among AI/AN
populations;
• Development and evaluation of
culturally appropriate interventions for
tobacco use prevention and cessation
targeted to AI/AN populations;
• Studies of how tobacco related
attitudes and behaviors in youth and
adults are influenced by ceremonial
tobacco use and other cultural factors;
• Studies of tobacco use behavior in
relation to different products, including
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dual use of cigarettes and smokeless
tobacco;
• Research on the characteristics, use,
and health effects of traditional tobacco
products, such as Iqmik;
• Research to understand disparities
in tobacco use within AI/AN
populations given substantial variations
by region and other factors; and
• Studies to identify and address
barriers to treatment among AI/ANs.
References
1. Tobacco Use Among Adults—United
States, 2005. MMWR. October 27, 2006; 55:
1145–1148.
2. Racial/Ethnic Differences Among Youths
in Cigarette Smoking and Susceptibility to
Start Smoking—United States, 2002–2004.
MMWR. December 1, 2006; 55; 1275–1277.
3. Renner CC, Patten CA, Day GE, Enoch
CC, Schroeder DR, Offord KP, Hurt RD,
Gasheen A, Gill L. Tobacco use during
pregnancy among Alaska Natives in western
Alaska. Alaska Med. 2005;47:12–16.
4. Burgess D, Fu SS, Joseph AM,
Hatsukami DK, Solomon J, van Ryn M.
Beliefs and experiences regarding smoking
cessation among American Indians. Nicotine
Tob Res. 2007;9 Suppl 1:S19–28.
For additional information about NCI
tobacco research contact: Mark
Parascandola, PhD, Epidemiologist,
Tobacco Control Research Branch,
National Cancer Institute, 6130
Executive Blvd. MSC 7337, Executive
Plaza North, Room 4039, Bethesda, MD
20892, Phone: 301–451–4587, Fax: 301–
496–8675, E-mail:
paramark@mail.nih.gov.
National Heart, Lung, and Blood
Institute (NHLBI)
Cardiovascular and Respiratory
Research
The NHLBI has a strong history of
supporting research to document and
intervene on health disparities among
AI/ANs, including the Strong Heart
Study, Pathways, Genetics of Coronary
Artery Disease in Alaska Natives
(GOCADAN), the Stop Atherosclerosis
in Native Diabetics Study (SANDS), and
Community-Responsive Interventions to
Reduce Cardiovascular Risk in AI/ANs.
The Strong Heart Study showed that
many AI/AN communities bear a heavy
burden of cardiovascular disease (CVD)
and cardiovascular risk factors (e.g.,
obesity, diabetes) that could be reduced
through effective interventions on
modifiable risk factors. The high burden
of disease will worsen unless behaviors
and lifestyles affecting CVD risk can be
changed. Prevalence of obesity in AI/AN
communities is about 50% higher than
in the U.S. general population, in which
obesity is often described as being of
epidemic proportions. In some AI/AN
communities, cigarette smoking,
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sedentary lifestyle, and stress augment
the adverse effects of obesity. AI/ANs
are particularly vulnerable to Type 2
diabetes, a problem exacerbated by high
rates of obesity. Diabetes prevalence is
3–20 fold higher among AI/ANs than in
the general U.S. population. It is an
important cause of coronary heart
disease, cardiomyopathy, end-stage
renal disease, non-traumatic
amputation, and vision impairment.
Lipid abnormalities also are common in
Type 2 diabetics, particularly high
triglycerides and low HDL-cholesterol
levels. Dyslipidemia and blood pressure
can be improved by appropriate changes
in diet and by increased exercise. CVD
risk is also substantially improved by
smoking cessation. In addition,
attention to high stress levels, untreated
sleep disordered breathing, short sleep
duration, and depression may be
warranted, because of evidence that
they may influence the health behaviors
of interest. For example, poorer diet,
higher smoking rates, and physical
inactivity are more prominent in those
with high stress, sleep disorders, or
depression. These psychosocial factors
also are associated with CVD
progression in observational
epidemiologic studies, and there is
evidence from smaller clinical studies
that they may affect mechanisms
leading to CVD. NHLBI is interested in
supporting research in AI/AN
communities that promotes the
adoption of healthy lifestyles and/or
improves behaviors related to
cardiovascular risk, such as weight
reduction, regular physical activity, and
smoking cessation. These behaviors and
lifestyles are known to affect biological
cardiovascular risk factors, such as
hypertension, dyslipidemia, obesity,
glucose intolerance, and diabetes. In
addition, control of these risk factors by
guideline-based use of antihypertensive,
lipid lowering, and hypoglycemic drugs
can reduce their adverse consequences.
However, these pharmacological
interventions are often suboptimally
utilized in AI/AN communities. The
NHLBI is interested in reducing
cardiovascular disease mortality and
morbidity in AI/AN, whether by
lifestyle changes, drug interventions, or
combinations thereof.
Lifestyles characterized by sleeping
less than 7 hours per night are
associated with increased risk of CVD,
obesity, diabetes, and all-cause
mortality. Insufficient sleep and poor
sleep quality is associated with
abnormalities in hypothalamic-pituitary
axis function and behavioral stress.
Sleep deprivation compromises
vigilance, judgment, mood, emotional
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expression, and other aspects of
cognition increasing the risk of unstable
patterns of behavior. The ability of sleep
deprivation to enhance the encoding
and recall of emotional (relative to
neutral) memories may profoundly
influence social interactions and stress.
Insufficient sleep is associated with an
increased risk of new onset substance
abuse and relapse, and new onset
depression and relapse. Intervention
studies to assess the efficacy of
improving sleep as part of a healthy
lifestyle or assessing how improving
sleep disorders could improve CVD
outcomes would be of interest to
NHLBI. Sleep disordered breathing
appears to be 30–60% more common
among American Indians than other
racial and ethnic groups. Sudden infant
death syndrome occurs 2.5 times more
frequently in AI/AN children than in
white children, and 2.0 times more
frequently than in the U.S. population
as a whole.
AI/AN also have been documented to
exhibit high rates of chronic respiratory
disease. AI/AN adults have the highest
asthma rate among single-race groups.
Recent evidence suggests that 11.6
percent of AI/AN suffer from asthma.
This is significantly higher than the
national average of 7.5 percent, and
much higher than every other single
racial or ethnic group. Chronic
obstructive pulmonary disease (COPD),
which includes emphysema and chronic
bronchitis, is the sixth leading cause of
death from chronic disease for AI/AN
men and the seventh leading cause of
death for women. AI/AN have the
second highest rates of cystic fibrosis
following whites. One in 10,500 AI/AN
has cystic fibrosis compared with one in
3,200 whites. Pueblo Indians and Zuni
Indians have higher incidence than
among other AI/AN Tribes. NHLBI is
interested in supporting research in AI/
AN communities that includes studies
of approaches to improve clinical
delivery of efficacious treatments of
chronic lung disease and their risk
factors, improved methods of chronic
lung disease self-management, studies
to promote or maintain respiratory
health or improved methods of
rehabilitation for diseases of the lungs
and airways, such as asthma, COPD,
cystic fibrosis; sleep disordered
breathing, occupational lung diseases,
pulmonary vascular disease or
pulmonary complications of AIDS.
In addition to these areas of research,
the NHLBI recognizes a unique and
compelling need to promote diversity in
the biomedical, behavioral, clinical, and
social sciences research workforce. The
NHLBI expects efforts to diversify the
workforce to lead to:
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• The recruitment of the most
talented researchers from all groups;
• An improvement in the quality of
the educational and training
environment;
• A more balanced perspective in the
determination of research priorities;
• An improved capacity to recruit
subjects from diverse backgrounds into
clinical research protocols; and
• An improved capacity to address
and eliminate health disparities.
For more information, please contact:
Jared B. Jobe, Ph.D. (Cherokee), Program
Director, Clinical Applications and
Prevention Branch, Division of
Prevention and Population Sciences,
National Heart, Lung, and Blood
Institute, 6701 Rockledge Drive, Suite
10018, MSC 7936, Bethesda, Maryland
20892–7936 (20817 express), Phone:
(301) 435–0407, Fax: (301) 480–5158, Email: JobeJ@mail.nih.gov.
National Institute of Arthritis and
Musculoskeletal and Skin Diseases
(NIAMS)
Research in Osteoporosis and other
Bone Diseases, Osteoarthritis,
Rheumatoid Arthritis and Skin Disease
Within the NIAMS Mission
The NIAMS supports efforts to
conduct research into the causes,
treatment, and prevention of arthritis
and musculoskeletal and skin diseases;
the training of basic and clinical
scientists to carry out this research; and
the dissemination of research progress
to improve the public health. Goals
specific to the AI/AN communities
involve research addressing the training
of underrepresented minority AI/AN
researchers and ensuring inclusion of
Native communities in clinical research
studies. NIAMS actively monitors the
inclusion of minority populations in
clinical research and will highlight any
grants that specifically target AI/AN
populations. The mission of the NIAMS
is to support research into the causes,
treatment, and prevention of arthritis
and musculoskeletal and skin diseases,
the training of basic and clinical
scientists to carry out this research, and
the dissemination of information on
research progress in these diseases.
Studies in these mission areas as they
relate to the AI/AN population may be
proposed.
For additional information about
research in these areas contact: Dr. Phil
Tonkins, National Institute of Arthritis
and Musculoskeletal and Skin Diseases,
6701 Democracy Blvd., Suite 800,
Bethesda, MD 20912, Phone: (301) 594–
4979, Fax: (301) 480–1284, E-mail:
tonkinsw2@mail.nih.gov.
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National Center for Complementary and
Alternative Medicine (NCCAM)
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Research on Traditional Healing
Practices
Many AI/AN communities use
traditional healing practices to prevent
and/or treat diseases and to maintain
health. NCCAM is interested in
supporting research on traditional
healing practices with these goals in
mind. NCCAM is also interested in
research on the safe and effective
integration of conventional care with
traditional healing practices for AI/AN
communities. The methodological
feasibility for integration has yet to be
addressed for many traditional healing
practices. Consequently, NCCAM is
interested in supporting developmental
studies to identify and address difficult
methodological and design issues
particular to traditional healing
practices, as well as to allow for the
development of contextually and
culturally sensitive research mirroring
the values of AI/AN communities.
Examples of study areas of interest
include, but are not limited to:
• Qualitative research to characterize
and document healing practices and
diagnostic approaches of indigenous
peoples, and study the feasibility of
research on those practices and
approaches in future clinical studies;
• Observational studies to explore
patient and care provider preferences,
beliefs, attitudes, and patient-provider
interactions;
• Case-control, observational, and
other studies to understand traditional
healing strategies from multiples
perspectives, including: (a) Optimal
dosing, duration, and frequency of
treatment; (b) type of treatment; (c)
examinations of different healing
practices to treat a particular disease/
condition; (d) comparisons of complex
versus simple interventions; (e)
evaluation of adherence among patient
populations to interventions with
varying levels of complexity; and (f)
examination of potentially important
individual differences that mediate or
moderate treatment outcome;
• Studies to determine if traditional
healing practices can be translated into
a broader clinical setting, in terms of:
Reliability, responsiveness and utility;
assessment procedures, instruments,
and tools in psychosocial, functional,
and physiological domains;
• Studies to construct and validate
culturally sensitive data collection
instruments; to design and pilot
outcome measures consistent with the
tenets of traditional, indigenous systems
of medicine and comparisons of these
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outcome measures to those commonly
used by conventional biomedicine; and
• Health services research of
established AI/AN traditional healing
practices to explore the factors that
influence access to and use of such
therapies; the nature, cost effectiveness,
and quality of such care; and ultimately
the effects on health and well-being.
For additional information on
NCCAM-supported research topics,
contact:
Sheila A. Caldwell, Ph.D., Program
Officer, Office of Special Populations,
National Center for Complementary and
Alternative Medicine, 6707 Democracy
Boulevard, Suite 401, MSC 5475,
Bethesda MD, 20892–5475, Phone: (301)
594–3396, Fax: (301) 480–3621, E-mail:
caldwells@mail.nih.gov.
Office of Research on Women’s Health
(ORWH)
Women’s Health Research
The ORWH at the NIH supports
research related to women’s health and
the study of sex and gender differences.
Detailed information about the NIH
Research Priorities for Women’s Health,
can be found at https://orwh.od.nih.gov/
research.html.
For additional information on
women’s health research, contact: Lisa
Begg, Dr. P.H., R.N., Director of
Research Programs, NIH Office of
Research on Women’s Health, 6707
Democracy Blvd., Suite 400, Bethesda,
MD 20892–5484, Phone: (301) 496–
7853, Fax: (301) 402–1798, E-mail:
beggl@od.nih.gov.
National Insitute of Mental Health
(NIMH)
Research projects aimed at
understanding the burden, treatment,
intervention or prevention of mental
disorders and Human
Immunodeficiency Virus (HIV)/AIDS in
AI/AN populations
Indigenous people in the United
States are disproportionately affected by
mental illness and HIV infection, as are
the larger racial and ethnic populations
such as African Americans and Latinos.
AI/ANs are highly underrepresented in
the physician workforce, as researchers,
and in health research in general,
numbering fewer than one hundred.
Other factors that contribute to
disparities that affect these communities
include geographic isolation, poor
access to health services,
underutilization of health services,
insufficient screening and partner
management services, social and
cultural norms, linguistics, stigma, and
gender. Research is needed to identify
and address the impact as well as the
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specific and unique aspects of mental
disorders and HIV infection upon
Native American communities. A
critical component of response to
mental health and HIV infection in
Native American communities will be to
identify, train, mentor, and develop
Native American investigators. Towards
these ends, a promising model is
community-based participatory research
together with community capacity
building.
Areas of interest to the NIMH that can
contribute to scientific knowledge about
mental health and HIV interventions in
Native Americans include, but are not
limited to research studies:
• To investigate the clinical
epidemiology of mental disorders and
HIV infection across all clinical and
service settings (e.g., primary care);
• To investigate research methods/
community assessment to eliminate
mental health disparities;
• To evaluate the impact of traumatic
stress and other social, cultural,
interpersonal, and environmental
factors on risk for and course of mental
disorders;
• To examine patient, provider, and
contextual factors that influence
diagnosis, help-seeking decisions and
preferences, and the helping
relationship;
• To understand processes
underlying HIV and mental illness
stigmas and discrimination in Native
American communities;
• To develop and assess effective
strategies and approaches for reducing
HIV and mental illness stigmas and
discrimination;
• To evaluate the effectiveness of
treatment, pharmacologic, psychosocial
(psychotherapeutic and behavioral),
somatic, rehabilitative, and combination
interventions on mental and behavior
disorders—including acute and longerterm therapeutic effects on functioning
for children, adolescents, and adults;
• To develop and tailor/target
interventions to communities/
individuals of Native Americans;
• To employ interventions that
improve quality and outcomes of care
(including diagnostic, treatment,
preventive, and rehabilitation services);
• To conduct scientifically rigorous
investigations of culturally appropriate
interventions, prevention, and control
strategies;
• To employ services interventions
that remove barriers to care leading to
the elimination of mental health
disparities;
• To conduct studies of services
organization, delivery (process and
receipt of care), and related health
economics at the individual, clinical,
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program, community, and systems
levels in specialty mental health,
general health, and other delivery
settings (such as the workplace,
schools);
• To enhance research infrastructure
and build research capacity for
conducting intervention and services
research;
• To explore alternative approaches
(e.g., telehealth) to translating,
delivering, implementing, and
disseminating mental health care;
• To investigate adaptation,
evaluation, safety, and costs of proven
interventions;
• To explore dissemination and
implementation strategies at multiple
organizational levels; and
• To examine the role of community
stakeholders in the research process,
especially readiness for change.
For additional information on NIMH
NonAIDS Applications contact: Carmen
P. Moten, Ph.D., Chief, Primary Care,
Socio Cultural and Disparities Research
Programs, Division of Services and
Intervention Research, National Institute
of Mental Health, 6001 Executive
Boulevard, Room 7131, MSC 9631,
Bethesda, MD 20892–9631, Phone: (301)
443–3725, Fax: (301) 443–4045, E-mail:
cmoten@mail.nih.gov.
For additional information on NIMH
HIV/AIDS-related applications contact:
David M. Stoff, Ph.D., Chief, HIV/AIDS
Neuropsychiatry Program, AIDS
Research Training and HIV/AIDS
Disparities Program, Division of AIDS
and Health and Behavior Research,
National Institute of Mental Health,
6001 Executive Boulevard, Room 6210,
MSC 9619, Bethesda, MD 20892–9619,
Phone: (301) 443–4625, Fax: (301) 443–
9719, E-mail: dstoff@mail.nih.gov.
For additional information on NIMH
research on Stigma and Health
Disparities contact: Emeline Otey, Ph.D.,
Chief, Stigma and Health Disparities
Program, Division of AIDS and Health
and Behavior Research, National
Institute of Mental Health, 6001
Executive Boulevard, Room 6227, MSC
9615, Bethesda, MD 20892–9615,
Phone: (301) 443–9284, Fax: (301) 480–
2920, E-mail: eotey@mail.nih.gov.
National Institute of Biomedical
Imaging and Bioengineering (NIBIB)
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Research in Technology for Health
The National Institute of Biomedical
Imaging and Bioengineering (NIBIB) is
committed to reducing health
disparities through the development of
new and affordable biomedical
technologies. To this end, the NIBIB is
interested in supporting the translation
of biomedical technologies that target
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the health needs of AI/AN communities.
Specifically, the NIBIB is interested in
supporting the development of
technologies that have broad therapeutic
and interventional applications as well
as technologies that complement
technology development in all program
areas of the NIBIB, https://
www.nibib.nih.gov/Research/
ProgramAreas.
For additional information about
NIBIB programs contact: John W. Haller,
Ph.D., National Institute of Biomedical
Imaging and Bioengineering, NIH/
DHHS, 6707 Democracy Blvd., Suite
200, Bethesda, MD 20892–5649, Phone:
(301) 451.4780, Fax: (301) 480.1614, Email: John.Haller@nih.hhs.gov.
National Eye Institute (NEI)
Vision Research
The NEI supports research and health
information dissemination with the goal
of protecting and prolonging the vision
of the American people. Examples of
such activity that may be of interest
include, but are not limited to:
• Epidemiological studies to
determine the prevalence and possible
risk factors of eye diseases and disorders
among AI/AN populations;
• Basic research studies into the
causes and mechanisms of eye diseases
and visual impairments in AI/AN,
research into disparities in access to
ophthalmic/optometric health services;
and,
• Development and evaluation of
culturally appropriate health education
and intervention.
For additional information on vision
research topics contact: Jerome R.
Wujek, Ph.D., National Eye Institute,
2020 Vision Place, Bethesda, MD
20892–3655, Phone: (301) 451–2020,
Fax: (301) 402–0528, E-mail:
wujekjer@nei.nih.gov.
THE OMISSION ABOVE OF ANY NIH
INSTITUTE, CENTER, OFFICE, OR
RESEARCH AREA SHOULD NOT BE
TAKEN AS A LACK OF AVAILABILITY
OF SUPPORT FOR PROJECTS IN
THOSE AREAS. NARCH is an NIH-wide
partnership, led at NIH by the National
Institute of General Medical Sciences
(NIGMS). General research priorities for
all of the individual NIH Institutes,
Centers, Divisions and Offices can be
found on their respective Web sites at:
https://www.nih.gov/icd/.
However, applicants and potential
academic partners are reminded that the
NARCH program is focused on the
research needs of the tribes and not
those of the federal or academic
partners.
Previous NARCH grants have been
funded by the following partners:
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• National Institute of General
Medical Sciences (NIGMS);
• National Cancer Institute (NCI);
• National Heart, Lung, and Blood
Institute (NHLBI);
• National Human Genome Research
Institute (NHGR);
• National Institute on Alcohol Abuse
and Alcoholism (NIAAA);
• National Institute of Allergy and
Infectious Diseases (NIAID);
• National Institute of Arthritis and
Musculoskeletal and Skin Diseases
(NIAMS);
• National Institute of Dental and
Craniofacial Research (NIDCR);
• National Institute of Diabetes and
Digestive and Kidney Diseases (NIDDK);
• National Institute on Drug Abuse
(NIDA);
• National Center for Complementary
and Alternative Medicine (NCCAM);
• National Center on Minority Health
and Health Disparities (NCMHD);
• NIH Office of Behavioral and Social
Sciences Research (OBSSR);
• NIH Office of Research on Women’s
Health (ORWH); and
• Agency for Healthcare Research and
Quality (AHRQ).
In addition to these partners within
HHS, the Federal Collaborative on
Health Disparities Research (FCHDR),
Headquartered in the HHS Office of
Minority Health (OMH) is in the process
of seeking co-funding partnerships for
the NARCH program with other
departments and agencies of the Federal
Government. Any additional
information that develops after the
publication of this announcement will
be posted on the NARCH program Web
site at https://www.ihs.gov/
MedicalPrograms/Research/narch.cfm
and disseminated to the
TECHASSISTANCE-NARCH listserve
developed from persons e-mailing their
contact information to narch@ihs.gov.
Public Policy Requirements: All
Federal-wide public policies apply to
IHS grants with exception of the
Lobbying and Discrimination public
policy.
3. Submission Dates and Times
A. Letter of Intent Deadline: March 15,
2009
Prospective applicants are asked to
submit a letter of intent that includes
the title of the new project(s) proposed,
the name, address, and telephone
number of the project Principal
Investigator(s), the identities of the
partners and of key personnel, and the
number and title of this RFA. The letter
of intent should be received before 5
p.m. Eastern Standard Time on March
15, 2009, by Mushtaq A. Khan, D.V.M.,
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Ph.D., Chief, Digestive and Respiratory
Sciences IRGs, Center for Scientific
Review, MSC 7818, Room 2176; 6701
Rockledge Drive; Bethesda, MD 20892
(20817 for express or courier service).
Phone: (301) 435–1778; Fax (301) 451–
2043; E-Mail: khanm@csr.nih.gov.
Letters may be submitted by mail, fax
or e-mail. Although a letter of intent is
not required, is not binding, and does
not enter into the review of a
subsequent application, the information
that it contains allows the IHS and NIH
Center for Scientific Review (CSR) staffs
to estimate the potential review
workload and avoid conflict of interest
in the review.
B. Application Deadline: May 14, 2009
The applications must be received
before 5 p.m. Eastern Standard Time on
May 14, 2009, at the Center for
Scientific Review (CSR) National
Institutes of Health, 6701 Rockledge
Drive, Room 6160—MSC 7892,
Bethesda, MD 20892–7720, Bethesda,
MD 20817 (for express or courier
service). Phone: (301) 435–0715) and at
the IHS Division of Grants Operations
(DGO) Indian Health Service, Reyes
Building, 801 Thompson Avenue, TMP
Suite 360, Rockville, MD 20852–1627
[zip code is unchanged for express/
courier services], Phone: (301) 443–
5204. Applications received after this
date will be returned to the applicant.
Competing applications not meeting the
deadline date specified in the
announcement are considered late
applications and will not be considered
for funding under this announcement.
The CSR will not accept any application
in response to this RFA that is
essentially the same as one currently
pending initial review, unless the
applicant withdraws the pending
application.
The CSR will not accept any
application that is essentially the same
as one already reviewed. This does not
preclude the submission of substantial
revisions of applications already
reviewed, but such applications must
include an introductory letter
addressing the previous critique.
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4. Intergovernmental Review
This funding opportunity is not
subject to Executive Order 12372,
‘‘Intergovernmental Review of Federal
Programs.’’ A State approval is not
required.
5. Funding Restrictions
• Pre-award costs are allowable
pending prior approval from the
awarding agency. However, in
accordance with 45 CFR part 74 all preaward costs are incurred at the
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recipient’s risk. The awarding office is
under no obligation to reimburse such
costs if for any reason the applicant
does not receive an award or if the
award to the recipient is less than
anticipated.
• The available funds are inclusive of
direct and appropriate indirect costs.
• Only one grant/cooperative
agreement will be awarded per
applicant under this announcement.
• IHS will not acknowledge receipt of
applications.
• Grantees are allowed a reasonable
period of time in which to submit
required financial and performance
reports. Failure to submit required
reports within the time allowed may
result in suspension or termination of
an active grant, withholding of
additional awards for the project, or
other enforcement actions such as
withholding of payments or converting
to the reimbursement method of
payment. Continued failure to submit
required reports may result in the
imposition of special award provisions,
or cause other eligible projects or
activities involving that grantee
organization, or the individual
responsible for the delinquency to not
be funded. Failure to obtain prior
approval for change in Scope, Principal
Investigator, Grantee Institutions,
Successor in Interest, or Recipient
Institute Name, undertaking any
activities disapproved or restricted as a
condition of the award, may result in
fund restrictions.
6. Other Submission Requirements
Each submitted research project
(including pilot research projects) must
be budgeted so that it could stand on its
own. That is, each project should be
fundable under its own budget so that
it could be completed even if none of
the rest of the NARCH is funded. All
things vital to each project should be
included in the budget of that project
and not included in the core. The
NARCH core should include only
administrative, training or other items
that are non-essential to the research
projects. The core should also include
the capacity to take advantage, for
training purposes, of any new research
opportunity that becomes available to
the grantee, whether through NARCH
funding or other new resources. The
core should be budgeted as if it were an
additional project and the total amounts
requested on the face page of the
NARCH application should represent
the sum of the projects plus the core.
Each subcontractor participating in each
project (or core) should submit its
budget as part of that project’s budget,
using appropriate form pages from the
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78581
PHS 398. Each project submission
should include a set of budget pages
from each of the institutional partners
participating in that project. Each
research project budget should
explicitly include that portion of the
grantee’s indirect costs that are
associated with activities under that
project, including direction and
oversight of the subcontracts. Each
project (and core) must include a
checklist and face page for that project.
Only the main face page for the entire
NARCH is required to have the
signatures of the NARCH principal
investigator and official signing for the
applicant organization.
Submit a typed and signed original
application, including the checklist, and
one single-sided photocopy of the entire
application (including Appendices and
supporting documents) in one package
to: Division of Grants Operations, Indian
Health Service, Reyes Building, 801
Thompson Avenue, TMP Suite 360,
Rockville, MD 20852–1627 (zip code is
unchanged for express/courier services),
Phone: (301) 443–5204.
At the time of submission, applicants
must also send four additional singlesided photocopied and signed
applications, including the Checklist,
Appendices, and supporting
documentation to: Center for Scientific
Review, National Institutes of Health,
6701 Rockledge Drive, Room 6160--MSC
7892, Bethesda, MD 20892–7720,
Bethesda, MD 20817 (for express or
courier service). Phone: (301) 435–0715.
The CSR no longer accepts hand
delivered applications. E-mail or other
electronic applications will not be
accepted under this announcement.
Specific supplementary instructions
for the PHS 398 application and budget
preparation for the NARCH program
may be obtained from the initiative
contacts listed under VII. Agency
Contacts, and will be posted at https://
www.ihs.gov/MedicalPrograms/
Research/narch.cfm. They will also be
sent to any potential applicant who emailed their contact information to
narch@ihs.gov with the words
‘‘technical assistance’’ in the subject
heading.
DUNS Number
Applicants are required to have a Dun
and Bradstreet (DUNS) number to apply
for a grant or cooperative agreement
from the Federal Government. The
DUNS number is a nine-digit
identification number, which uniquely
identifies business entities. Obtaining a
DUNS number is easy and there is no
charge. To obtain a DUNS number,
access https://
www.dunandbradstreet.com or call 1–
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866–705–5711. Interested parties may
wish to obtain their DUNS number by
phone to expedite the process.
A DUNS number is required before
Central Contractor Registry (CCR)
registration can be completed. Many
organizations may already have a DUNS
number. Please use the number listed
above to investigate whether or not your
organization has a DUNS number.
Registration with the CCR is free of
charge.
Applicants may register by calling 1–
888–227–2423. Please review and
complete the CCR Registration
Worksheet located at https://
www.grants.gov/CCRRegister.
More detailed information regarding
these registration processes can be
found at https://www.grants.gov.
Electronic Research Administration
(eRA) User Name
Each NARCH Application’s Principal
Investigator is required to have a user
name with the NIH eRA system. This
also requires that the applicant
institution (Tribe or Tribal organization)
be an eRA Commons Registered
Organization. A list of eRA Commons
Registered Organizations can be found
at https://era.nih.gov/commons/
quick_queries/
commons_registered_orgs.cfm. More
information on the eRA Commons
system can be found at https://
era.nih.gov/.
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V. Application Review Information
Upon receipt, IHS and NIH staff will
administratively review applications for
completeness and responsiveness.
Applications that are incomplete, nonresponsive to this RFA, or do not follow
the guidelines of the PHS form 398
(revised 11/2007) or of the
supplementary instructions for NARCH
grants (available at: https://www.ihs.gov/
MedicalPrograms/Research/narch.cfm
or from narch@ihs.gov), may be returned
to the applicant without further
consideration. Applications will be
evaluated in accordance with the
criteria stated below for scientific and
technical merit by appropriate peer
review groups convened by the CSR.
The National Advisory General Medical
Sciences Council will conduct the
second level of review.
1. Criteria
Priorities for funding will be based on
the scientific and technical merit of the
application, the assessed potential of
investigators in the developmental
stages of their careers, and the
likelihood that the proposed project(s)
can further the purposes of the NARCH
initiative. Awards will be made only to
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organizations with financial
management systems and management
capabilities that are acceptable under
HHS policy. Awards will be
administered under the HHS Grants
Policy Statement, January 2007.
A. Review of Student and Faculty/
Researcher Development Plans
The anticipated effectiveness of the
proposed NARCH in making a
difference relative to the current baseline data (based in part on previous
experience of the NARCH) will be
assessed. Factors to be considered
include:
• The appropriateness of the content,
phasing, quality, and duration of the
student or faculty/researcher
development plans in the NARCH
application to achieve the scientific
development of the faculty/researcher,
post-doctoral, pre-doctoral,
undergraduate, and (if well justified)
high school students; and
• The research experience and
expertise, proposed commitment, and
quality of the mentoring plan and of
individual mentors of the partners in
providing mentoring, guidance, and
advice to candidates (including training
in responsible conduct of research and
research integrity, teaching, and
protection of human subjects), and in
fostering the development of academic
and community-based AI/AN
researchers.
B. Review of Research Projects
The NIH has announced procedures
to be used for the review of research
grant applications (NIH Guide, Volume
26, Number 22, June 27, 1997 or see
https://grants.nih.gov/grants/guide/
notice-files/not97-010.html and https://
grants.nih.gov/grants/guide/notice-files/
NOT-OD-05-002.html for additional
updated information.) For NARCH
applications, the five criteria listed in
this announcement will be used for the
scientific review of research projects
and pilot research projects. The review
of research projects and pilot research
projects will be the same except that
applications for pilot studies may be
smaller in scope and would not be
expected to have preliminary data.
In the written comments, reviewers
will be asked to discuss the following
aspects of the application in order to
judge the likelihood that the proposed
research will have a substantial impact
on the pursuit of these purposes. Each
of these criteria will be addressed and
considered in assigning the overall
score, weighting them as appropriate for
each application.
• Significance: Does this study
address an important problem? If the
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aims of the application are achieved,
how will scientific knowledge or
clinical practice be advanced? What will
be the effect of these studies on the
concepts, methods, technologies,
treatments, services, or preventative
interventions that drive this field?
• Approach: Are the conceptual or
clinical framework, design, methods,
and analyses adequately developed,
well integrated, well reasoned, and
appropriate to the aims of the project?
Does the applicant acknowledge
potential problem areas and consider
alternative tactics?
• Innovation: Is the project original
and innovative? For example: Does the
project challenge existing paradigms or
clinical practice; address an innovative
hypothesis or critical barrier to progress
in the field? Does the project develop or
employ novel concepts, approaches,
methodologies, tools, or technologies for
this area?
• Investigators: Are the investigators
appropriately trained and well suited to
carry out this work? Is the work
proposed appropriate to the experience
level of the principal investigator and
other researchers? Does the investigative
team bring complementary and
integrated expertise to the project (if
applicable)?
• Environment: Does the scientific
environment in which the work will be
done contribute to the probability of
success? Do the proposed studies
benefit from unique features of the
scientific environment, or subject
populations, or employ useful
collaborative arrangements? Is there
evidence of institutional support?
In reviewing the overall Center, the
initial scientific review group will
examine evidence of the partners’
commitment to the purposes of the
NARCH initiative to develop a cadre of
AI/AN scientists and health
professionals engaged in biomedical,
clinical, behavioral and health services
research that is competitive for Federal
funding; to increase the capacity of both
research-intensive institutions and AI/
AN organizations to work in partnership
to reduce distrust by AI/AN
communities and people toward
research; and to encourage competitive
research linked to the health priorities
of the AI/AN partner and to reducing
health disparities.
The evidence will include:
• The quality of the partnership of the
institutional and community partners,
and the quality of the involvement of
the Community and Scientific Advisory
Council, as demonstrated by
documentation of (for instance): The
intellectual and tangible contributions
and activities of the partners, and of the
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Council, in developing the application
and the proposed NARCH; the
interactions of the partners, and of the
members of the Council, in meetings
(such as those to develop the
application and proposed NARCH); the
past activities and future plans to
increase the capacity of the partners and
of the Council; the plans for future
contributions and activities by the
partners, and by the Council, in
furthering the goals of the proposed
NARCH; and the plans for future
development of the partnership itself;
• The experience and commitment of
the institutional and community
partners to recruit, retain, and advance
AI/AN faculty/ researcher and students,
to support faculty/researcher and
student research efforts, and to increase
the role of the involved AI/AN
communities in the plans of the
proposed NARCH;
• The appropriateness of the plan for
evaluating the impact of the proposed
NARCH, including the quality of
baseline data and milestones for
accomplishments, and a system to track
the future course of program
participants; and
• The potential of the proposed
NARCH to be a regional and national
resource, including: Capacity to provide
quality research training and mentoring
for integrated promotion and
development of AI/AN research careers
from undergraduate (or if well justified,
high school) through post-doctoral
levels; attainment of quality research
linked to health priorities of the AI/AN
partner and to reducing health
disparities; plans for research
information dissemination and
education activities; and plans for the
development of research networks to
support the scientific aims of the
proposed NARCH. For competitive
renewal applications, reviewers will
also assess the previous
accomplishments and progress of the
applicants.
In addition to the above criteria, in
accordance with NIH policy, all
applications will also be reviewed with
respect to the following:
• The adequacy of plans, if research
on human subjects is involved, to
include both genders and children as
appropriate for the scientific goals of the
research. Plans for the recruitment and
retention of subjects will also be
evaluated.
• For applications that are competing
renewals of existing NARCH centers,
has significant progress been achieved
toward each of the originally proposed
projects?
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• The reasonableness of the proposed
budget and duration in relation to the
proposed research.
• The adequacy of the proposed
protection for humans, animals or the
environment, to the extent they may be
adversely affected by the project
proposed in the application.
• The adequacy of the proposed plan
to share data, if appropriate.
VI. Award Administration Information
1. Award Notices
The Notice of Award (NoA) will be
initiated by the IHS Division of Grants
Operations (DGO) and will be mailed
via postal mail to each entity that is
approved for funding under this
announcement. The NoA will be signed
by the Grants Management Officer and
this is the authorizing document for
which funds are dispersed to the
approved entities. The NoA will serve
as the official notification of the grant
award and will reflect the amount of
Federal funds awarded, the purpose of
the grant, the terms and conditions of
the award, the effective date of the
award, and the budget/project period.
The NoA is a legally binding document.
Applicants who are approved but
unfunded or disapproved based on their
objective review score will receive a
copy of the Executive Summary which
identifies the weaknesses and strengths
of the application submitted.
2. Administrative and Policy
Requirements
A. Grants are administrated in
accordance with the following
documents:
• This Announcement.
• Administrative Requirements: 45
CFR part 92, (Uniform Administrative
Requirements for Grants and
Cooperative Agreements to State, Local
and Tribal Governments, (or 45 CFR
part 74, (Uniform Administrative
Requirements for Awards to Institutions
of Higher Education, Hospitals, Other
Non-Profit Organizations, and
Commercial Organizations.
• Grants Policy Guidance: HHS
Grants Policy Statement, January 2007.
• Cost Principles: OMB Circular A–
87, (State, Local, and Indian (Title 2 Part
225).
• Cost Principles: OMB Circular A–
122, (Non-profit Organizations (Title 2
Part 230).
• Audit Requirements: OMB Circular
A–133, (Audits of States, Local
Governments, and Non-profit
Organizations).
B. Inclusion of Women and Minorities
in Research Involving Human Subjects:
It is the policy of the NIH that women
and members of minority groups and
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their subpopulations must be included
in all NIH supported biomedical,
clinical, behavioral, and health services
research projects involving human
subjects, unless a clear and compelling
rationale and justification is provided
that inclusion is inappropriate with
respect to the health of the subjects or
the purpose of the research. This policy
results from the NIH Revitalization Act
of 1993 (Section 492B of Pub. L. 103–
43). Because the NARCH initiative
targets AI/AN people and communities,
a minority population, only the policy
of inclusion of women applies to this
RFA. The IHS has fully accepted the
Office for Human Research Protections
(OHRP) policy regarding human
subjects. The OHRP Web site is https://
www.hhs.gov/ohrp/. All investigators
proposing research involving human
subjects should read the Updated NIH
Guidelines for Inclusion of Women and
Minorities as Subjects in Clinical
Research, published in the NIH Guide
for Grants and Contracts on August 2,
2000. (https://grants.nih.gov/grants/
guide/notice-files/NOT-OD-00048.html). The complete Guidelines are
available at: https://grants1.nih.gov/
grants/funding/women_min/
guidelines_amended_10_2001.htm . The
revisions relate to NIH defined Phase III
clinical trials and require:
• All applications or proposals and/or
protocols to provide a description of
plans to conduct analyses, as
appropriate, to address differences by
sex/gender and/or racial/ethnic groups,
including subgroups if applicable; and
• All investigators to report accrual,
and to conduct and report analyses, as
appropriate, by sex/gender and/or
racial/ethnic group differences.
C. Inclusion of Children as Participants
in Research Involving Human Subjects
It is the policy of NIH that children
(i.e., individuals under the age of 21)
must be included in all human subjects
research, conducted or supported by the
NIH, unless there are scientific or
ethical reasons not to include them.
This policy applies to all initial (Type
1) applications submitted. All
investigators proposing research
involving human subjects should read
the NIH Policy and Guidelines on the
Inclusion of Children as Participants in
Research Involving Human Subjects that
was published in the NIH Guide for
Grants and Contracts, March 6, 1998,
and is available at the following URL
address: https://grants.nih.gov/grants/
guide/notice-files/not98–024.html.
Investigators may obtain copies of these
policies from the initiative staff listed
under VII. Agency Contacts. Initiative
staff may also provide additional
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relevant information concerning the
policy.
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D. URLS in NIH Grant Applications or
Appendices
All applications and proposals for
NIH funding must be self-contained
within specified page limitations.
Unless otherwise specified in an NIH
solicitation, Internet addresses (URLs)
should not be used to provide
information necessary to the review
because reviewers are under no
obligation to view the Internet sites.
Reviewers are cautioned that their
anonymity may be compromised when
they directly access an Internet site.
E. Allowable Administrative Costs
Certain administrative costs for
managing a comprehensive program are
allowable and may vary, depending
upon the size and complexity of the
program’s activities. The costs budgeted
for NARCH grants and subcontracts may
not duplicate items already budgeted in
other cost centers of the AI/AN,
research-intensive, and subcontracted
organizations and institutions, such as
accounts which make up the Facilities
and Administration (F&A) cost pool.
The grantee organization receiving the
award must be prepared to provide
documentation showing the direct
relationship of proposed costs to the
program, and that costs of this type are
charged in a uniform manner to all other
grants at all institutions and
organizations participating in the award.
Limited salary support for secretarial
or clerical help is allowable only when
in direct support of the proposed
NARCH project. For guidance,
applicants should refer to the OMB
Circular appropriate for them, A–87
(Cost Principles for State, local, and
Indian Tribal Governments), at https://
www.whitehouse.gov/omb/circulars or
A–122 (Cost Principles for Non-Profit
Organizations), at https://
frwebgate.access.gpo.gov/cgi-bin/
leaving.cgi?from=leavingFR.html&log=
linklog&to=https://https://
www.whitehouse.gov/omb/circulars, or
should contact the Grants Management
Officer listed under VII. Agency
Contacts.
Costs for evaluation activities are
allowable, as are costs for the
Community and Scientific Advisory
Council. All research project
applications must include costs
associated with one annual meeting per
year in Rockville, MD, of the project
Principal Investigator(s) and their key
scientific personnel. Research project
applications should also include costs
associated with attendance for key
personnel and presenters to the annual
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Native Health Research Conference.
NARCH core and/or training budgets
should include these travel costs for key
NARCH personnel and trainees who are
not associated with specific research
projects.
Student Development Costs: Student
(graduate, undergraduate, and high
school if well justified) remuneration
through salary/wages for participation
in research experiences may be
requested, provided all the following
conditions are met:
I. The student is performing necessary
work involved in the research;
II. There is an employer-employee
relationship between the student and
the proposed NARCH or its partners;
III. The total compensation is
reasonable for the work performed; and
IV. It is the practice of the proposed
NARCH or its partners to provide
compensation for all students in similar
circumstances, regardless of the source
of support for the activity.
Graduate students, but not
undergraduate students, are allowed
tuition costs as part of a compensation
package. When requesting support for a
graduate student, the NARCH
application should provide, in the
budget justification section of the
application, the basis for the
compensation level. The IHS staff will
review the requested compensation
level and, if it is reasonable and
justified, will provide compensation up
to a maximum of $45,000 (https://
grants.nih.gov/grants/guide/notice-files/
not98-168.html). Post-doctoral students
should be compensated at a rate
commensurate with that of other postdoctoral employees with similar degrees
and experience at the research-intensive
institution. It is the expectation of the
IHS and NIGMS that students who are
enrolled in a accredited graduate
program, as part of a proposed NARCH,
will not be excluded from support from
other non-Federal or Federal graduate
training sources (such as loans and
assistance under the Veterans’
Adjustment Benefit Act or Pell Grants)
for which they are eligible.
Graduate and post-doctoral students
cannot concurrently hold other
Federally-sponsored stipends or
fellowship or any other Federal award
that duplicates the NARCH support.
Faculty/Researcher Development Costs
Costs to support faculty/researcher
development activities, such as
workshops or courses, national
meetings, or short-term research
experiences in the laboratory of an
active NIH-extramurally-funded
researcher needed for acquiring specific
skills or methodologies needed for
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prospective research, are allowable.
Such costs might include tuition, travel
and per diem costs, as well as salary
support appropriate to the percent effort
needed for the activity.
Research Project Costs
Direct costs associated with research
and pilot research projects are allowable
when adequate justification is provided.
These include faculty/researcher
salaries, reimbursed according to
percent effort. Summer salary support
can be paid provided the institution’s
academic schedule permits such release
and when the institution approves. The
maximum summer-salary support
provided by the program cannot exceed
the equivalent of three months at 100
percent effort, or time specified by the
institution as its policy. Grant funds
may not be used to increase or
supplement faculty/researcher academic
year salaries. Salary support for
technical assistance and costs for
consultants, if justified, are allowable.
Costs for equipment to be used to carry
out the proposed research are allowable.
Cost for Supplies
Costs for supplies, including costs for
animals necessary to carry out the
proposed research, may be included.
Travel costs for the investigator(s) and
staff are permitted to required meetings
or when direct benefits to the program
are expected, and when adequate
justification is provided. Alterations and
renovations costs (up to $40,000) are
allowable only when essential for
conduct of the proposed research. Other
permitted costs include animal
maintenance (unit care costs and
number of care days), donor fees,
publication costs, computer charges,
rentals and leases, equipment
maintenance, and service contracts.
Consortium and Contract Arrangements
Consortium arrangements that may
involve personnel costs, supplies, and
other allowable costs, including
overhead costs; contractual costs for
support services, such as the laboratory
testing of biological materials, clinical
services, data processing, or core
administrative services, are allowable
expenses. Consortia and contractual
costs with Native health organizations,
Tribes and/or research institutions in
Canada or Mexico are allowable
expenses.
Pilot Research Projects
The intent of pilot research projects is
to lead to regular research projects
funded as part of the center grant or as
freestanding grants. For pilot research
projects, applications may request
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support for up to $75,000 (direct costs)
per year for up to four years. Pilot
research investigators considering
project periods of less than four years
are encouraged to consider the fact that
initiation of a new research activity in
a new population often takes much
longer than originally anticipated and
that the creation of a trusting
relationship between the investigator
and the community is both vital and
time consuming. NARCH pilot research
support is non-renewable. However,
NARCH research projects based on prior
NARCH pilot research projects are
encouraged.
Subcontracts
The grant recipient may issue
subcontracts to other organizations
(such as the research-intensive
institution of the partnership), as long as
a minimum of 30 percent of the grant
funds are budgeted in the application to
remain with the eligible AI/AN
organization(s); that is, no more than 70
percent of the application’s total budget
may be contained in subcontract
budgets of the non-eligible
subcontracting partner institutions or
organizations.
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F. Unallowable Costs
Unallowable costs for research
projects (including for pilot projects)
include costs for student development,
textbooks, journals, memberships, and
Internet subscription costs, as well as
other costs prohibited by OMB Circulars
A–87 or A–122 as applicable.
Employees of the applicant organization
may not serve as paid consultants but
may be paid. The pilot research project
is intended for faculty/researcher
without current Federal research
support. Therefore, investigators with
significant current support from other
mechanisms such as the R01 and
research funding from other extramural
sources are not eligible, and the costs
therefore are not allowable. Release time
for preparing proposals or mini-research
projects, not submitted as pilot projects,
is not allowed.
G. Research Subjects Protection
Under governing policy, Federal
funds administered by the HHS shall
not be expended for research involving
live vertebrate animals without prior
approval by the NIH Office of
Laboratory Animal Welfare (OLAW), of
an assurance to comply with the Public
Health Service (PHS) Policy on Humane
Care and Use of Laboratory Animals.
This restriction applies to all
performance sites (e.g., collaborating
institutions, subcontractors,
subgrantees) without OLAW-approved
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assurances, whether domestic or
foreign. Funds included in this award
may not be used to support studies
using live vertebrate animals until
approval from the Institutional Animal
Care and Use Committee (IACUC) has
been received by the IHS Grants
Management Officer (GMO).
Federal Regulations (45 CFR, Part 46)
require that applications and proposals
involving human subjects must be
evaluated with reference to the risks to
the subjects, the adequacy of protection
against these risks, the potential benefits
of the research to the subjects and
others, and the importance of the
knowledge gained or to be gained.
Under governing regulations 45 CFR
part 46, found at https://www.hhs.gov/
ohrp/humansubjects/guidance/
45cfr46.htm, Federal funds
administered by HHS shall not be
expended for research involving human
subjects, and individuals shall not be
enrolled in such research, without prior
approval by the Office for Human
Research Protections (OHRP), of an
appropriate Federal Wide Assurance
(FWA) and prior approval by an
Institutional Review Board (IRB)
recognized and listed by the OHRP.
Funds included in this award may not
be used to support studies using human
subjects until evidence of IRB approval
has been received by the IHS GMO.
Grantees are expected to provide their
own institutional FWA.
H. Research Integrity
Grantees shall comply with Public
Health Service Policies on Research
Misconduct (42 CFR part 93) which
require grantees to have procedures for
responding to allegations of research
misconduct that comply with those
policies, to submit their procedures to
the Office of Research Integrity (ORI)
(https://ori.hhs.gov) upon request for
review, and revise their procedures in
accordance with ORI comments. In
addition, grantees shall file the Annual
Report on Possible Research Misconduct
with ORI at https://www.ori.dhhs.gov/
assurance/electronic_submission.shtml.
Grantees shall file documentation of
their Annual Reports with the IHS
GMO.
I. Healthy People 2010
The Public Health Service (PHS) is
committed to achieving the health
promotion and disease prevention
objectives of Healthy People 2010, a
PHS led national activity for setting
priority areas. This RFA announcement
is related to one or more of the priority
areas. Potential applicants may obtain a
copy of Healthy People 2010 at:
https://www.healthypeople.gov.
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3. Indirect Costs
This section applies to all grant
recipients that request reimbursement of
indirect costs in their grant application,
but not to the indirect costs that may be
negotiated by the grantees with their
subcontractors (which become direct
costs to the grantee). In accordance with
HHS Grants Policy Statement, Part II–
27, IHS requires applicants to have a
current indirect cost rate agreement in
place prior to award. The rate agreement
must be prepared in accordance with
the applicable cost principles and
guidance as provided by the cognizant
agency or office. A current rate means
the rate covering the applicable
activities and the award budget period.
If the current rate is not on file with the
DGO at the time of award, the indirect
cost portion of the budget will be
restricted and not available to the
recipient until the current rate
documentation is provided to the DGO.
Generally, indirect costs rates for IHS
grantees are negotiated with the
Division of Cost Allocation https://
rates.psc.gov/ and/or the Department of
the Interior (National Business Center)
https://www.nbc.gov/acquisition/ics/
icshome.html. If your organization has
questions regarding the indirect cost
policy, please contact the DGO at (301)
443–5204.
4. Reporting
A. Progress Report. Program progress
reports are required semi-annually.
These reports will include a brief
comparison of actual accomplishments
to the goals established for the period,
or, if applicable, provide sound
justification for the lack of progress, and
other pertinent information as required.
A final annual progress report,
cumulative from the beginning of the
project period, must be submitted
within 90 days of expiration of each
budget period.
B. Financial Status Report. Quarterly
financial status reports must be
submitted within 30 days of the end of
each quarter. Final financial status
reports are due within 90 days of
expiration of the budget/project period.
Standard Form 269 (long form) will be
used for financial reporting.
C. Reports. Grantees are responsible
and accountable for accurate reporting
of the Progress Reports and Financial
Status Reports. Financial Status Reports
(SF–269) are due 90 days after each
budget period and the final SF–269
must be verified from the grantee
records on how the value was derived.
Grantees must submit reports in a
reasonable period of time.
Failure to submit required reports
within the time allowed may result in
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suspension or termination of an active
grant, withholding of additional awards
for the project, or other enforcement
actions such as withholding of
payments or converting to the
reimbursement method of payment.
Continued failure to submit required
reports may result in one or both of the
following: (1) The imposition of special
award provisions; and (2) the nonfunding or non-award of other eligible
projects or activities. This applies
whether the delinquency is attributable
to the failure of the grantee organization
or the individual responsible for
preparation of the reports.
5. Telecommunication for the Hearing
Impaired is Available at: TTY (301)
443–6394.
VII. Agency Contact(s)
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1. Questions on the initiative
regarding IHS NARCH issues and
policies may be directed to: Alan
Trachtenberg, M.D., M.P.H., Division of
Planning, Evaluation and Research,
Indian Health Service, 801 Thompson
Avenue, TMP Suite 450, Rockville, MD
20852, Phone: (301) 443–4700, Fax:
(301) 443–0114, e-mail: narch@ihs.gov.
2. Questions on grants management
and fiscal matters may be directed to:
Sylvia Ryan, Division of Grants
Operations, Indian Health Service,
Reyes Building, 801 Thompson Avenue,
TMP Suite 350, Rockville, MD 20852,
Phone: (301) 443–5204, Fax: (301) 443–
9602, e-mail: narch@ihs.gov.
3. Questions on NIH and NIGMS
issues and policies, may be directed to:
Clifton A. Poodry, Ph.D., Minority
Opportunities in Research Division,
National Institute of General Medical
Sciences, 45 Center Drive, Suite 2AS.37,
MSC 6200, Bethesda, MD 20892, Phone:
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(301) 594–3900, Fax: (301) 480–2753, email: poodryc@nigms.nih.gov.
4. Questions on the review of
applications may be directed to:
Mushtaq A. Khan, D.V.M., Ph.D., Chief,
Digestive and Respiratory Sciences
IRGs, Center for Scientific Review, MSC
7818, Room 2176; 6701 Rockledge
Drive; Bethesda, MD 20892 (20817 for
courier or express service) Phone: (301)
435–1778; Fax: (301) 451–2043; e-mail:
khanm@csr.nih.gov.
VIII. Other Required Documents
If the applicant is a federallyrecognized Tribe, Tribal organization, or
a Tribal college, letters of support from
the Chairman, President, Governor, or
Tribal Health Director is required of all
Tribes to be served to show their
support of the grant project. Letters of
support are intended to document that
applicants have Tribal support for the
specific grant for which they are
applying. All letters of support must
accompany the grant application.
IX. Other Information
References for Background Information:
Anderson, N.B. Levels of analysis in health
science: A framework for integrating
sociobehavioral and biomedical research.
Annals of the New York Academy of
Sciences, 1998, 840, 563–576.
Ballantine, B., Ballantine, I. (Eds.),
Thomas, D.H., Miller, J., White, R., Nabokov,
P., Deloria, P.J. (Text by), Joseph, A.M.
(Intro.) The Native Americans: An Illustrated
History. Turner Publishing, Inc. Atlanta, GA,
1993.
Freeman, W.L. The role of community in
research with stored tissue samples. Weir R
(Ed.) Stored tissue samples: Ethical, legal,
and public policy implications. University
Iowa Press. Iowa City, IA, 1998, 267–301.
Gazmararian, J.A., Baker, D.W., Williams,
M.V., Parker, R.M., Scott, T.L., Green, D.C.,
Fehrenbach, S.N., Ren, J. & Koplan, J.P.
Health literacy among Medicare enrollees in
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Sfmt 4703
a managed care organization. Journal of the
American Medical Association, 1999, 281,
545–551.
Haynes, M.A. & Smedley, B.D. (Eds.) The
Unequal Burden of Cancer: An Assessment of
NIH Programs for Ethnic Minorities and the
Medically Underserved. Institute of
Medicine. National Academy Press.
Washington, DC, 1999.
Macaulay, A.C., Commanda, L.E., Freeman,
W.L., Gibson, N., McCabe, M.L., Robbins,
C.M., & Twohig, P.L., (for the) North
American Primary Care Research Group.
Participatory research maximizes community
and lay involvement. British Medical Journal,
1999, 319, 774–778.
Minority Economic Profiles. U.S. Bureau of
the Census, Population Division. Issued July
24, 1992. (Tables 1990 CPH–L–92, 93, 94 and
95).
NIH Publication 98–4247. Women of Color
Health Data Book. Office of Research On
Women’s Health, National Institutes of
Health, 1998.
Trends in Indian Health 1998–99. Program
Statistics Team, Office of Public Health,
Indian Health Service, 2001.
Regional Differences in Indian Health
1998–99. Program Statistics Team, Office of
Public Health, Indian Health Service, 2000.
Weiss, B.D., Reed, R.L., & Kligman, E.W.
Literary skills and communication methods
of low-income older persons. Patient
Education and Counseling, 1995, 25, 109–
119.
Williams, D.R. & Collins, C. U.S.
Socioeconomic and Racial Differences in
Health: Patterns and Explanations. Annual
Review of Sociology, 1995, 21, 349–386.
Williams, M.V., Parker, R.M., Baker, D.W.,
Parikh, N.S., Pitkin, K., Coates, W.C., &
Nurss, J.R. Inadequate functional health
literacy among patients at two public
hospitals. Journal of the American Medical
Association, 1995, 274, 1677–1682.
Dated: December 15, 2008.
Robert G. McSwain,
Director, Indian Health Service.
[FR Doc. E8–30300 Filed 12–19–08; 8:45 am]
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[Federal Register Volume 73, Number 246 (Monday, December 22, 2008)]
[Notices]
[Pages 78570-78586]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E8-30300]
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Part VII
Department of Health and Human Services
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Indian Health Service
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Native American Research Centers for Health (NARCH) Grants; Notice
Federal Register / Vol. 73, No. 246 / Monday, December 22, 2008 /
Notices
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Indian Health Service
Native American Research Centers for Health (NARCH) Grants
Announcement Type: New and Competing Continuations.
Funding Announcement Number: HHS-2010-IHS-NARCHVI-0001.
Catalog of Federal Domestic Assistance Numbers (s): 93.933.
Key Dates: Letter of Intent Deadline: March 15, 2009.
Application Deadline Date: May 14, 2009.
Review Date: October, 2009.
Earliest Anticipated Start Date: June 1, 2010.
I. Funding Opportunity Description
The Indian Health Service (IHS), in conjunction with the National
Institute of General Medical Sciences (NIGMS) and other institutes of
the National Institutes of Health (NIH) announces competitive grant
applications for Native American Research Centers for Health (NARCH),
an initiative to support new and/or continuing centers or projects
funded under the NARCH grant program. This funding mechanism will
develop further opportunities for conducting research and research
training to meet the needs of American Indian/Alaska Native (AI/AN)
communities. This program is authorized under the Snyder Act, 25 U.S.C.
13, the Public Health Service Act, 42 U.S.C. 241 as amended, and the
Indian Health Care Improvement Act, 25 U.S.C. 1602(a)(b)(16). This
program is described at 93.933 in the Catalog of Federal Domestic
Assistance.
Background Information:
The AI/AN Tribal nations and communities have long experienced
health status worse than that of other Americans. Although major gains
in reducing health disparities were made during the last half of the
twentieth century, most gains stopped by the mid-1980s (Trends in
Indian Health 1998-99) and a few diseases, e.g., diabetes, worsened.
''All Indian'' rates contain marked variation among the IHS Areas or
regions (Regional Differences in Indian Health 1998-99); and variation
by Tribe exists within Areas as well. The Trends and Regional
Differences reference can be found at the IHS Web site at: https://
www.ihs.gov/NonMedicalPrograms/IHS_Stats. Although the AI/AN mortality
rates for all cancers are about 20 percent lower than the U.S. rates
for all races, there is variation among IHS Areas for specific cancers.
Moreover, the favorable AI/AN mortality rates for some cancers may be
due to markedly lower incidence rates partly offset by higher case-
fatality rates. Unfamiliarity with modern health care may adversely
influence health status among the elderly, the low-income elderly, and
Tribes, and also may reduce the acceptability of health research among
them. The daunting tasks confronting Tribes, researchers, and health
care and public health programs in the beginning of the twenty-first
century are to resume the reduction of health disparities that had
occurred through the 1980s, to reverse the worsening in a few diseases,
to maintain and strengthen the favorable status, and to reduce the
disparities among and within Areas and Tribes. Factors known to
contribute to health status and disparities are complex, and include
underlying biology, physiology, and genetics, as well as ethnicity,
culture, socioeconomic status, gender/sex, age, geographical access to
care, and levels of insurance.
Additional factors known to contribute to health status and
disparities include:
1. Family, home, and work environments;
2. General or culturally specific health practices;
3. Social support systems;
4. Lack of access to culturally appropriate health care; and
5. Attitudes toward health.
Yet none of these alone, or in combination, accounts for all
documented differences. Health disparities of AI/ANs may also reflect a
lack of in-depth research relevant to improving their health status.
Many AI/ANs distrust research for historical reasons. One approach that
combats this distrust is to ensure that Tribes are the managing
partners in training and research that involves them, as for example,
in community-based participatory research (i.e., a collaborative
research process between researchers and community representatives).
This approach is especially helpful to design both training relevant to
researchers from Tribal communities, and research relevant to the
health needs of the communities.
Research Objectives:
The NARCH initiative will support partnerships between Federally
recognized AI/AN Tribes or Tribal organizations (including national and
area Indian health boards, and Tribal colleges meeting the definition
of a Tribal organization as defined by 25 U.S.C. 1603(d) or (e)) and
institutions that conduct intensive academic-level biomedical,
behavioral and health services research. These partnerships are called
Native American Research Centers for Health (NARCH). Due to the
complexity of factors contributing to the health and disease of AI/ANs,
and to their health disparities compared with other Americans, the
collaborative efforts of the agencies of the Department of Health and
Human Services (HHS) and the collaboration of researchers and AI/AN
communities are needed to achieve significant improvements in the
health status of AI/AN people. To accomplish this goal, in addition to
objectives set by the Tribe, Tribal organization or Indian health
boards, the IHS NARCH program will pursue the following program
objectives:
To develop a cadre of AI/AN scientists and health
professionals--Opportunities are needed to develop more AI/AN
scientists and health professionals engaged in research, and to conduct
biomedical, clinical, behavioral and health services research that is
responsive to the needs of the AI/AN community and the goals of this
initiative. Faculty/researchers and students at each proposed NARCH
will develop investigator-initiated, scientifically meritorious
research projects, including pilot research projects, and will be
supported through science education projects designed to increase the
numbers of, and to improve the research skills of, AI/AN investigators
and investigators involved with AI/ANs.
To enhance partnerships and reduce distrust of research by
AI/AN communities--Recent community-based participatory research
suggests that AI/AN communities can work collaboratively in partnership
with health researchers to further the research needs of AI/ANs. Fully
utilizing all cultural and scientific knowledge, strengths, and
competencies, such partnerships can lead to better understanding of the
biological, genetic, behavioral, psychological, cultural, social, and
economic factors either promoting or hindering improved health status
of AI/ANs, and generate the development and evaluation of interventions
to improve their health status. Community distrust of research and
researchers will be reduced by offering the Tribe greater control over
the research process.
To reduce health disparities--In the Indian Health Care
Improvement Act, Public Law 94-437 (as amended), IHS was legislatively
mandated to improve the delivery of effective health care to AI/ANs. In
the NIH Revitalization Act of 1993, NIH was encouraged to increase
[[Page 78571]]
the number of under-represented minorities participating in biomedical,
clinical, and behavioral research, including studies on drug abuse and
alcoholism, and the examination of the role of resiliency in the
prevention and treatment of those conditions. Also, the ``Initiative to
Eliminate Racial and Ethnic Disparities in Health'' by HHS (https://
www.omhrc.gov/rah) encouraged NIH to help reduce health disparities. In
response to these priorities, the IHS and NIH have established a
collaboration to support the NARCH.
Reducing health disparities among AI/AN communities and individuals
may be fostered by greater understanding of how to enhance their
strengths and resilience. While AI/AN communities have relied on health
research and medical science to reduce health disparities, they have
also relied on their own psychological, organizational, and cultural
assets and strengths to survive major harms and disruptions over the
centuries, and to rebound from insults to health.
The mission of NIH is to acquire new knowledge that will lead to
better health by understanding the processes underlying health and
disease that in turn will help prevent, detect, diagnose, and treat
disease and disability. The NARCH initiative works toward the NIH
mission by supporting research that discovers the interrelationships
among the many factors that contribute to health and disease, and by
helping to train and promote AI/AN researchers and researchers
concerned with AI/AN health.
II. Award Information
Type of Awards: Grant.
Estimated Funds Available: The estimated funds (total costs)
available for the first year of support for the entire initiative is
expected to be at least $2.0 million in Fiscal Year 2010. The actual
amount may vary, depending on the response to the request for
applications (RFA) and availability of funds. An applicant may request
a project period not to exceed four years of support, and direct costs
not to exceed $1,100,000 per center or $550,000 per project (research
or training) in the first year of each award. Direct costs to the
applicant include the total cost of each subcontract (subcontractor
direct plus subcontractor indirect costs).
Anticipated Number of Awards: An estimated five to fifteen awards
will be made under the program.
Award Amount: $100,000-$1,100,000 per year.
III. Eligibility Information
The new or existing NARCH must be a working partnership of the
eligible AI/AN organization and of the research-intensive institution.
Applicants eligible to receive the NARCH award are Federally recognized
Tribes and Tribal organizations as defined under the Indian Health Care
Improvement Act, 25 U.S.C. 1603 (d) or (e), including eligible Indian
health boards or Tribal colleges applying on behalf of eligible
Federally recognized Tribes or Tribal organizations. As the grantee,
the eligible AI/AN organization will define criteria and eligibility
for participation in all aspects of the partnership, consistent with
this announcement. A minimum of 30 percent of the grant funds must be
budgeted in the application to remain with the eligible AI/AN
organization(s); that is, no more than 70 percent of the application's
total budget may be contained in subcontract budgets of the non-
eligible subcontracting partner institutions or organizations.
1. Eligible Applicants--The AI/AN applicant must be one of the
following:
A federally recognized AI/AN Tribe, as defined under 25
U.S.C. 1603(d); or
A Tribal organization, as defined under 25 U.S.C. 1603(e),
including Tribal colleges or health boards meeting this definition; or
A consortium of two or more of those Tribes or Tribal
organizations. Applicants other than Tribes must provide proof of non-
profit status.
2. Cost Sharing or Matching--The NARCH program does not require
matching funds or cost sharing.
3. The Research-Intensive Partner--The Research-Intensive Partner
must be an accredited public or private nonprofit university, academic
medical center, or other institution that has an established record of
conducting research into the health problems of AI/AN; has demonstrated
a commitment to enhancing the capability of AI/AN faculty/researchers,
students, investigators, and communities to engage in biomedical,
behavioral, clinical and health services research; and has demonstrated
a commitment to mentoring AI/AN faculty/researchers, students, and
investigators.
4. Principal Investigator--The Principal Investigator, the
individual responsible for the administration (including fiscal
management) of the overall project, must have his/her primary
appointment with the AI/AN applicant organization. Special arrangements
of employment, such as inter-organizational personnel agreements, are
permissible. The Principal Investigator may be, but is not required to
be, the NARCH Program Director or a Research Project Investigator. The
NARCH Principal Investigator may or may not have formal academic/
research credentials, but if not, then the NARCH Program Director must
be so qualified.
The traditional NIH research project grant consists of a single
Principal Investigator (PI) working with a small group of subordinates
on an independent research project. Although this model clearly
continues to work well and encourages creativity and productivity, it
does not always work well for multidisciplinary efforts and
collaboration. Increasingly, health-related research involves teams
that vary in terms of size, hierarchy, location of participants, goals,
disciplines, and structure. There is growing consensus that team
science would be encouraged if more than one PI could be recognized on
individual awards. The NIH has adopted a multiple-PI model, as recently
directed by the Office of Science and Technology Policy. All agencies
that have research and research-related programs must offer the
multiple-PI model as an option. Note, it is only an option, not a
requirement. The traditional NARCH division of roles between PI and
Project Director will usually address these issues to a satisfactory
degree. For additional information regarding the new multiple-PI model,
please click on the following website: https://grants.nih.gov/grants/
multi_pi/index.htm.
5. NARCH Program Director--The NARCH Program Director is the
individual responsible for the day-to-day leadership and management of
the research and training programs within the proposed NARCH. The
Program Director may be, but is not required to be, the Student and
Faculty/Researcher Development Director or a Research Project
Investigator. The NARCH Program Director may or may not have formal
academic/research credentials, but if not, then the Principal
Investigator must be so qualified.
6. Student and Faculty/Researcher Development Director and
Participant--The NARCH initiative is an institutional developmental
grant mechanism that places an emphasis on the continual development of
students and faculty/researchers. If a new Student and/or Faculty/
Researcher Development Program is proposed in the current application,
then the Principal Investigator of that project is expected to be the
NARCH Student and Faculty Development Director. In order to be included
as the Student and Faculty
[[Page 78572]]
Development Director, the prospective director must have a faculty/
researcher appointment at the research-intensive institution (or
equivalent appointment at the AI/AN organization or other consortium
partner) and must demonstrate that he/she has the knowledge, skills,
and capabilities to mentor students and faculty/researchers and to
generate and direct development and mentoring programs.
The Student and Faculty Development Director may be the NARCH
Program Director. Faculty/researchers and students should be supported
in research education activities that improve their skills and
abilities to be successful at the next stage of their professional
development. To be included as a participant for faculty/researcher
development in the proposed NARCH, the individual must have a faculty/
researcher appointment at the research-intensive institution or
equivalent appointment at the AI/AN organization or consortium partner.
7. Research Project Investigators--The NARCH initiative is an
institutional developmental grant mechanism that places an emphasis on
continual improvement of the research competitiveness of the research
investigators. In order to be included as a research project
investigator in the NARCH, a prospective investigator must have a
faculty appointment at the research-intensive institution or equivalent
appointment at the AI/AN organization or other consortium partner, and
must show that he/she has the need, based on institutional,
departmental, and professional development plans, to enhance his/her
research knowledge, skills, and capabilities by engaging in the
proposed research program and associated activities.
8. Tribal Approval of the Application--It is the policy of the IHS
that all research involving AI/AN Tribes be approved by the Tribal
governments with jurisdiction. Therefore, the following documentation
is required as part of the application for new or continuing centers or
additional NARCH projects:
Tribal Resolution:
If the applicant is an Indian Tribe or Tribal organization, a
resolution supporting the project from the Tribal government of all
Tribes to be served must accompany the application submission.
Applications by Tribal organizations will not require resolutions if
the current Tribal resolutions under which they operate would encompass
the proposed activities. In this instance, a copy of the current
resolution must accompany the application. The listed Tribes to be
served by the project in the proposal must match the set of appended
resolutions. If a resolution from an appropriate representative of each
Tribe to be served is not submitted prior to October 1, 2009, the
application will be considered incomplete and will not be considered
for funding.
An official signed resolution must be received by October 1, 2009
by the Division of Grants Operations (DGO), IHS, at the Reyes Building,
801 Thompson Avenue, TMP 360, Rockville, MD 20852. A grant will not be
awarded unless the signed resolution is received. Please include the
funding opportunity number, as a reference to this announcement, if the
resolutions are submitted as a separate mailing.
9. Mechanism of Support--Awards under this initiative will be
administered using the competing institutional grant mechanism of the
IHS, and will be reviewed using the NIH S06 mechanism.
IV. Application and Submission Information
1. Address to Request Application Package: NARCH Program Official,
Reyes Building, 801 Thompson Avenue, Rockville, MD 20852 or by e-mail
to narch@ihs.gov. Applicants are strongly encouraged to establish
eligibility of their proposed applications prior to submission.
Inquiries about eligibility should be addressed to Alan Trachtenberg,
M.D., M.P.H., at (301) 443-0578 or by e-mail to narch@ihs.gov. The
application package, including supplemental instructions will be posted
on the IHS Research Program Web site, at: https://www.ihs.gov/
MedicalPrograms/Research/narch.cfm. Technical assistance will be made
available for applicants, and first time applicants are urged to take
advantage of it. To sign up for technical assistance, potential
applicants should e-mail their contact information to narch@ihs.gov
with the words ``technical assistance'' in the subject heading and full
contact information, including email address, listed in the body of the
e-mail.
The NIH instructions for the PHS 398 application form are available
in an interactive format at: https://grants.nih.gov/grants/funding/
phs398/phs398.html. Applicants must use the currently approved version
of the PHS 398. For further assistance contact GrantsInfo, Telephone
(301) 435-0714, e-mail: GrantsInfo@nih.gov, Telecommunications for the
hearing impaired: TTY 301-451-0088.
Submit a typed and signed original application, including the
Checklist, and one (1) single-sided photocopy of the entire application
(including Appendices and supporting documents) in one package to:
Division of Grants Operations, Indian Health Service, Reyes Building,
801 Thompson Avenue, TMP 360, Rockville, MD 20852-1627 (zip code is
unchanged for express/courier services), Telephone: (301) 443-5204.
``Native American Research Centers for Health'' and the RFA number
NOT-GM-09-010 must be typed on line 2 of the face page of the
application form and the YES box must be marked.
At the time of submission, applicants must also send four (4)
additional single-sided photocopied and signed applications, including
the Checklist, Appendices, and supporting documentation to: Center for
Scientific Review (CSR), National Institutes of Health, 6701 Rockledge
Drive, Room 6160--MSC 7892, Bethesda, MD 20892-7720, Bethesda, MD 20817
(for express or courier service). Telephone: (301) 435-0715. The CSR no
longer accepts hand delivered applications. E-mail or other electronic
applications will not be accepted under this announcement.
Specific supplementary instructions for the PHS 398 application and
budget preparation for the NARCH program may be obtained from the
initiative contacts listed under VII. Agency Contacts, and will be
posted at: https://www.ihs.gov/MedicalPrograms/Research/narch.cfm. They
will also be sent to any potential applicant who e-mailed their contact
information to narch@ihs.gov with the words ``technical assistance'' in
the subject heading.
There will be no acknowledgment of receipt of the application.
2. Content and Form of Application Submission:
A proposed NARCH may include any or all of the following
components: Student development projects; faculty/researcher
development projects; research projects (including pilot projects); and
``core'' administrative facilities.
The content of the application should explain the components of the
application, and how they help meet the purposes of the NARCH
initiative. A description should be provided of the current state of
the research and research training enterprise at the proposed NARCH and
its institutional and community partners, including faculty/researcher
and student profiles.
A clear statement should be presented of the overall goals,
specific measurable objectives, and anticipated milestones. These
elements should be presented in the context of needed improvements in
the partners' organizational
[[Page 78573]]
infrastructure and environment for research. Documentation should be
provided to establish that the research-intensive partner is an
institution with a record of conducting research into the health of AI/
ANs, and that it has a demonstrated commitment to the special
encouragement of, and assistance to, AI/AN faculty/researchers,
students, investigators, and communities for enhancing their capacity
to engage in biomedical, behavioral and health services research. For
competitive renewals of existing NARCH grants, previous accomplishments
and progress from the time of the initial NARCH award must be
described. Documentation about the nature of the partnership itself
should be included, such as: the process to develop the application and
proposed NARCH itself, the past and future efforts to increase the
capacity of the partners to improve their partnership, and efforts to
contribute to the success of the NARCH. Applicants are encouraged to
articulate plans for the development of partnerships toward the
possible planning of a national native health research conference or
other national research training. The development of additional future
collaborative research and research training opportunities should also
be an integral part of each NARCH core proposal. For previously
existing NARCH centers, a specific and detailed list of accomplishments
and assessment of the benefits from the previous NARCH grant(s) is
required.
A plan for assessment of the benefits of the activities by the
proposed NARCH on specific, measurable outcomes identified in the
application should be provided. IHS and NIGMS recognize that Tribes,
Tribally-based organizations, and research-intensive institutions are
diverse in their missions, their health and economic status, and their
cultures. Such an assessment for a new NARCH could include a self-study
by the proposed NARCH and its partners, which focuses on fact-finding,
program evaluation, and recommendations for improvement in key areas.
Strategies for determining the initial and ongoing success of their
efforts for organizational development should also be presented. It is
expected that each proposed NARCH will develop its own set of
strategies that best match its circumstances. Guidance and suggestions
for program evaluation of a proposed NARCH can be obtained from https://
www.the-aps.org/education/promote/promote.html. For applications that
are competing renewals of existing NARCH centers, the report and
evaluation of the progress made under the previous NARCH grant(s) will
be a key part of the application.
Applicants are strongly urged to contact NARCH initiative staff at
an early stage to request the specific supplementary instructions for
the PHS 398 for the NARCH grants. Supplementary instructions may be
obtained from the initiative contacts listed under VII. Agency
Contacts, and will be posted at: https://www.ihs.gov/MedicalPrograms/
Research/narch.cfm. They will also be sent to any potential applicant
who e-mailed their contact information to narch@ihs.gov with the words
``technical assistance'' in the subject heading.
If Student Development Projects are proposed, the NARCH application
should describe new programs or modifications or additions to existing
programs of the partners that encourage and facilitate AI/AN students
to enter, advance, and remain in health research careers. Such projects
might include, but are not limited to, providing employment as research
assistants in research projects of research-active mentors with an
explicit mentoring plan, providing other mentoring with an explicit
mentoring plan, providing workshops to improve technical or
communication skills, providing motivating seminars or journal clubs
highlighting problems of interest to students, providing contact with
role models, and providing opportunities to travel to present results
at national scientific meetings. If research mentorships or
apprenticeships are proposed, the application should clearly document
the experience, proposed commitment, and quality of the mentors in
providing guidance and advice to students (including responsible
conduct of research and research integrity, teaching, and protection of
human subjects), and in fostering the development of academic and/or
community-based AI/AN researchers.
The application should describe how the development plans for the
students will meet both the individuals' professional development
goals, and one purpose of the NARCH initiative: To develop a cadre of
AI/AN scientists and health professionals. The application must have an
evaluation plan for the new project(s) that indicates the anticipated
outcomes relative to the current baseline data. For example, one
outcome might be the improved retention of AI/AN students in science
majors. The application should indicate the anticipated (quantitative)
improvement relative to the current retention rate. Accomplishments of
(and connections with) any previously funded NARCH student development
projects by the applicant or partners must be described.
A student in a NARCH Student Development Project must be a full-
time or part-time student officially enrolled in an educational program
leading to an undergraduate or graduate degree, or in a post-doctoral
educational program, or (if well justified) in late high school. A
helpful book about mentoring science students is found at https://
books.nap.edu/catalog/5789.html.
If Faculty/Researcher Development Projects are proposed, the NARCH
application should describe the need, proposed activity, and
anticipated outcomes. Faculty/researcher development projects might
include, but are not limited to, short-term mentored research
experiences in the lab of an active NIH-extramurally-funded researcher
with an explicit mentoring plan, long-term general mentoring under an
explicit mentoring plan, or attendance at workshops or courses or
national meetings needed for acquiring specific skills or methodologies
needed for prospective research. As with student development projects,
the application should document the experience, proposed commitment,
and quality of the mentors, teachers, or experience in providing
guidance and advice to faculty/researchers, and in fostering the
development of academic and community-based AI/AN research. The
application must also describe the evaluation plan for the faculty/
researcher development project. The application must clearly describe
how the development plans for faculty/researchers will meet both the
individuals' professional development goals, and two purposes of the
NARCH initiative:
To develop a cadre of AI/AN scientists and health
professionals, and
To enhance the partnership of the proposed NARCH.
For grantees with previous NARCH funding for faculty/researcher
development projects, a detailed list of the accomplishments of (and
connections with) any previously funded NARCH faculty/researcher
development projects by the applicant or partners must be described.
NARCH applications may include a maximum of five (5) regular
Research Projects and a maximum of five (5) Pilot Research Projects.
Unlike regular research projects, a pilot research project is limited
in scope and is not expected to have preliminary data. It is also
limited to a budget of no more than $75,000 direct costs per year for
four years. The pilot research project is intended for faculty/
researchers without current Federal research support.
[[Page 78574]]
Support for faculty/researchers participating in pilot research
projects is preparatory to seeking more substantial funding from NIH
research grant programs (e.g., Academic Research Enhancement Award, K,
and R01 awards), as well as funding from other agencies and private
sources. Funds received from the proposed NARCH to support pilot
research projects may not be used to supplement ongoing research
projects. A NARCH application need not include both research projects
and pilot research projects. Applications for only pilot research
projects or for only research projects may be submitted. Individual
project investigators may propose either a research project or a pilot
research project, but not both. For research projects that are
continuations or modifications or outgrowths of research projects
(including pilot research projects) under previous NARCH grants, the
accomplishments of the previous research project(s) should be detailed
and a logical description given as to how the results of the previous
work has led to the current proposal.
Each research project or pilot research project should follow the
instructions provided in PHS 398 (Revised 11/2007) for preparing
research grant applications. The professional development goals must
clearly describe specific objectives and milestones which should
include, but are not limited to, improving competitiveness in acquiring
grant support. The applicant should describe how successful completion
of the proposed research project will improve the research skills and
will help develop the students and faculty/researchers, thus
contributing to the overall goals and specific measurable objectives of
the proposed NARCH.
Each research project or pilot research project must follow the IHS
policy concerning Tribal approval, that all research involving AI/AN
Tribes be approved by the Tribal governments with jurisdiction. That
is, each grantee must include a resolution of approval from the Tribal
government(s), or (if applicable) a letter of support signed by the
Executive Director or CEO of the eligible AI/AN organization, or both
(if applicable) for projects that involve people or community(ies) of
an AI/AN Tribe, or an eligible Tribal organization. For NARCH proposals
from multi-Tribal consortia with projects that involve only one or a
few of the Tribes of the consortium, some description should be
provided as to the process through which the particular Tribes were
chosen to participate.
Research projects (including pilot research projects) proposed
under this initiative must be in research areas normally funded by any
of the NIH or other research agencies in the HHS. Research projects
addressing health disparities and the health priorities of the AI/AN
partner are especially encouraged.
A listing of grants recently funded by NIH may be found at Computer
Retrieval of Information on Scientific Projects (CRISP), a searchable
database of Federally-funded biomedical research projects conducted at
universities, hospitals, and other research institutions. It may be
accessed at https://report.nih.gov/crisp/crispquery.aspx. The following
agencies, institutes, offices, and centers have stated particular
interests in supporting research under the NARCH Program as follows:
National Institute of Dental and Craniofacial Research (NIDCR)
Oral Health Research
NIDCR is committed to reducing the disproportionate burden of oral
diseases experienced by AI/ANs. The focus of NIDCR's health disparities
research is on improving oral health status and quality of life by
understanding and addressing oral diseases that are prevalent in AI/AN
communities, specifically caries (including early childhood caries),
oral and pharyngeal cancer, and periodontal disease. Interdisciplinary
research teams and the full participation of communities are viewed by
NIDCR as essential components of any health disparities research.
Data that document oral disease prevalence are readily available
for some populations, but not for others. Homogeneity in subgroups of
populations cannot be assumed. For instance, there are national data
for Mexican Americans, but not for the numerous other Hispanic
subgroups. Similarly, data regarding the oral health status of various
AI/AN Tribes are unavailable. Moreover, available data provide little
insight into the etiology or determinants of oral disease and oral
health. The paucity of quality data and conceptual models concerning
the broad array of potential determinants and risk-factors inhibits
progress toward preventing disease, and improving oral health status
and quality of life. The NIDCR invites applications that, in
preparation for intervention research, explore the complex array of
social, behavioral, psychological, contextual, environmental, and
biological factors and their interactions that may contribute to oral
health disparities within AI/AN communities. Including oral health
status measures within broader epidemiologic studies is encouraged.
However, applications that are limited to the assessment of disease
prevalence and that explore a very limited range of potential
determinants will be considered non-responsive.
The NIDCR has particular interest in intervention research that
will provide clinically meaningful outcomes and essential information
needed to inform clinical practice, public health policy, health care
provision, community and/or individual action. Intervention studies
that are grounded in theory are needed. Both basic and applied
intervention research applications are invited. Studies may need to
intervene at multiple levels within communities. The NIDCR encourages
the use of the strongest research design possible and recognizes that
not all intervention research is amenable to randomized clinical
trials. Examples of health disparities intervention research of
interest to the NIDCR includes but are not limited to:
Effectiveness studies that tailor/target preventive
approaches to communities/individuals;
Research that intervenes in novel ways on macro- or
intermediate level determinants of oral health status;
Health services research that explores alternative
approaches to delivering preventive oral health care;
Studies that intervene on common risk factors or that take
a systems approach;
Studies that explore multifaceted strategies to intervene
at several levels within society;
Dissemination and implementation research at multiple
organizational levels; and
Research that uses appropriate technology for translation,
implementation, adoption, adherence, and acceptance of oral disease
prevention programs in defined populations, clinics, and communities.
Intervention research should be reasonably applicable to a specific
AI/AN population. To facilitate adequate enrollment and
generalizability, intervention studies may need to be conducted at
multiple sites. Studies may be conducted at a single site only if
enrollment is adequate and if sufficient numbers of participants are
available to allow extrapolation of clinically meaningful results to
the specific AI/AN population of interest.Pilot research projects that
are designed to lead to larger research projects funded as part of a
center or as
[[Page 78575]]
free-standing NIH grants may be proposed.
For additional information about oral health research contact: Ruth
Nowjack-Raymer, M.P.H., PhD, Director, Health Disparities Research
Program, National Institute of Dental and Craniofacial Research, 6701
Democracy Blvd., Room 640, Bethesda, MD 20892-4878, Phone: (301) 594-
5394, Fax: (301) 480-8322, e-mail: nowjackr@mail.nih.gov.
National Institute on Drug Abuse (NIDA)
Neuroscience and Drug Abuse Research:
AI/ANs demonstrate higher rates of drug abuse, particularly
methamphetamine, tobacco and alcohol abuse, relative to other racial
subgroups. According to 2002-2006 National Survey on Drug Use and
Health (NSDUH) data, AI/AN past year methamphetamine use was 1.4%
compared to 0.1% for African Americans, 0.6% for Hispanics or Latinos
and 0.7% for Whites. Prevalence of use is high in both men and women.
Drug abuse patterns among AI/AN are complex and can vary by factors
such as Tribe and geographic location. While some datasets are
available that can provide general epidemiological data regarding use
and abuse rates in this group, data are needed that better clarify
where use rates are highest, among which Tribes, age and gender groups
and the factors that predict drug abuse in these locales and groups.
These data will assist in developing more targeted interventions and in
identifying mechanisms related to drug abuse which can then serve as
focal points for intervention.
In addition to scarce data on patterns of use, limited data are
available assessing drug abuse prevention and treatment interventions
for AI/AN. The matrix model has been proposed in particular to address
methamphetamine abuse, but few data are available to assess the
efficacy of this approach with this population. Several preventive
interventions have been designed particularly for this population and
results from them indicate their value, but more research is needed to
clarify why these sometimes don't work in expected ways and whether the
interventions that are being used but have not been evaluated are
working to reduce drug use.
The NIDA is committed to reducing health disparities in drug abuse
and related health and social consequences among AI/AN. Further, the
Institute supports methodologies required by the NARCH, expecting that
studies be developed and implemented using community participatory
approaches.
Research topics of interest include but are not limited to:
Studies that explore a range of behavioral, cultural,
environmental, and individual factors that contribute to drug abuse;
Studies that explore the consequences of drug abuse among
AI/ANs;
Studies that consider the full context of drug abuse,
including poverty, family factors, school factors, intergenerational
trauma, etc.;
Studies that explore the role of traditional practices and
spirituality in protecting against drug abuse;
Studies that explore other factors that protect against
use in those groups for whom use rates are lower;
Studies that explore the efficacy and/or effectiveness of
culturally relevant preventive interventions;
Studies that explore the efficacy and/or effectiveness of
culturally relevant treatment interventions;
Studies that assess factors related to service
utilization, including use rates and access to services, either in
reservation or urban settings; and
Studies that explore the organization, management and
delivery of interventions.
For additional information about neuroscience or drug abuse
research contact: Kathy Etz, PhD, National Institute on Drug Abuse,
6001 Executive Blvd., Room 5153 MSC 9589, Bethesda, MD 20852, Phone:
(301) 402-1749, Fax: (301) 480-2543, e-mail: Kathleen.Etz@nih.hhs.gov.
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
Alcohol Research
NIAAA is committed to reducing the disproportionately high burden
of illness associated with alcohol use, abuse, and dependence among AI/
AN people. Alcohol-associated disability-adjusted life years (DALYs)
remain highest among AI/ANs in comparison to all other U.S. ethnic
groups. AI/AN people suffer from unacceptably high rates of alcohol
abuse and dependence, alcohol-related morbidity and mortality, and
intentional and unintentional injuries associated with alcohol use.
Nevertheless, AI/AN people are heterogeneous on many dimensions with
over 562 Federally-recognized Tribal entities. To address alcohol-
related health disparities of AI/AN people, more needs to be known
about how differences between Tribes, geographic regions, residence on
reservations, urban or rural areas, as well as more typical demographic
variables such as age, education, income, and gender influence alcohol
use and associated health status outcomes. Such information can guide
the development of more effective and culturally appropriate ways of
identifying and intervening with those who suffer from alcohol-related
problems, as well as preventing alcohol problems before they occur.
Additional research is also needed to understand how to best advance
the dissemination of research findings on alcohol and health, so that
AI/AN people can benefit from the latest research discoveries. Finally,
NIAAA is aware that oftentimes researchers who conduct investigations
among communities of color are members of these cultural, racial or
ethnic groups themselves. NIAAA is committed to identifying and
providing training and mentoring experiences to help AI/AN alcohol
researchers advance the science of alcohol use and give back to their
communities.
The NIAAA is committed to reducing alcohol related health
disparities and is committed to the NARCH program. Research topics of
interest to NIAAA include but are not limited to:
--Studies that assess the differing needs of various Tribal groups,
considering variations in rates of alcohol use, misuse and abstinence.
--Studies that develop new interventions or adapt existing prevention
and/or treatment interventions that take strengths of the AI/AN culture
into consideration.
--Studies that investigate the application/adaptation of evidence based
interventions among AI/AN groups.
--Studies that investigate how traditional spiritual and medical
treatments can be applied/adapted to improve intervention outcomes
among AI/AN peoples.
--Studies that explore the effectiveness and/or efficacy of commonly
used interventions such as screening and brief intervention or referral
among AI/AN populations.
--Studies that investigate the risk and protective factors associated
with drinking among women of childbearing age so as to inform
culturally sensitive, effective FASD prevention.
--Studies that investigate ways to delay onset of youth drinking among
AI/AN young people.
--Studies that investigate the association between alcohol use and
suicide among AI/AN people, especially youth. Studies may attempt to
understand the individual and
[[Page 78576]]
group level variables that contribute to ``epidemics'' of suicide among
AI/AN youth.
--Studies that explore the consequences of alcohol use and misuse among
AI/AN peoples; these consequences may include but are not limited to
other social and health problems (i.e., diabetes, obesity, poor
nutrition, cancer, liver disease, etc.), interfamilial violence,
intentional and unintentional injury, and driving under the influence.
--Studies that investigate the acceptance and efficacy of
pharmacotherapy for alcohol abuse and dependence within integrated
health counseling approaches.
--Studies that investigate the influence of alcohol use on the spread
and treatment of Human Immunodeficiency Virus (HIV)/Acquired Immune
Deficiency Syndrome (AIDS) among AI/AN peoples.
For additional information contact:
Judith A. Arroyo, PhD, Minority Health and Health Disparities
Coordinator, Project Official, Division of Epidemiology and Prevention
Research, National Institute on Alcohol Abuse and Alcoholism, 5635
Fishers Lane Room 2079, Bethesda, MD 20892-9304, (for Fed Ex use
Rockville, MD 20852-1705), Office: 301-402-0717, Fax: 301-443-8614, e-
mail: Judith.Arroyo@nih.hhs.gov.
National Cancer Institute (NCI)
Cancer Health Disparities Research
The Center to Reduce Cancer Health Disparities (CRCHD) is committed
to reducing cancer health disparities among AI/ANs. Investigators are
encouraged to submit research projects addressing every aspect of
cancer and cancer health disparities research. CRCHD welcomes
investigations in basic, clinical, translational, and population-based
research addressing cancer health disparities among AI/AN. The CRCHD is
central to the NCI's efforts to reduce the unequal burden of cancer in
our society. As part of these efforts, the Diversity Training Branch,
CRCHD, has been supporting NARCH projects with cancer relevance since
2003.
For additional information contact:
Dr. Peter Ogunbiyi, Program Director, Diversity Training Branch,
Center to Reduce Cancer Health Disparities, National Cancer Institute,
6116 Executive Boulevard, Suite 602, Bethesda, MD 20892-8341 (U.S.
Postal Service), Phone: 301-496-7344, Fax: 301-435-9225, e-mail:
po43t@nih.gov.
Health Literacy Research:
The HHS, in its Healthy People 2010 initiative, defines health
literacy as, ``the degree to which individuals have the capacity to
obtain, process, and understand basic health information and services
needed to make appropriate health decisions.'' (Please see: https://
www.healthypeople.gov/document/HTML/Volume1/11HealthCom.htm). Health
literacy is a complex phenomenon that involves individuals, families,
communities, and systems. For instance, consumers, patients,
caregivers, traditional healers, or other laypersons may vary with
respect to:
Access (e.g., to audience-appropriate information, media
or professionals);
Skills (e.g., to gather and comprehend health information;
to speak and share personal information about health history and
symptoms; to act on information by initiating appropriate follow-up
visits and conveying understanding back to the information source; to
make decisions about basic healthy behaviors, such as healthy eating
and exercise; to engage in self-care and chronic disease management);
Knowledge (e.g., of health and medical vocabulary,
concepts such as ``risk'', the organization and functioning of
healthcare systems, cultural beliefs and possible differences in
traditional and current medical systems about disease causation,
prevention and treatment);
Abilities (e.g., sensory, communication, cognitive, or
physical challenges or limitations);
Features of health care providers and public health
systems (e.g., the communication skills of health professionals,
platforms employed for patient education, built environments, and
signage);
Traditional healers and their role, especially in relation
to the existing medical systems which could lead to different
understanding in health and disease progression;
Demographics (e.g., developmental or life stage, cultural,
linguistic, or educational differences that affect health beliefs,
knowledge, and communication).
Too often people with the greatest health burdens have limited
access to relevant health information. One reason is the complex and
cumbersome ways in which health information is presented. Health care
professionals may not communicate effectively with individuals. For
instance, achieving informed consent for treatment is difficult when
health care personnel cannot explain biological processes or treatment
procedures in simplified language and patients cannot interpret health
information. These situations hamper the effectiveness of health
professionals' efforts to prevent, diagnose, and treat medical
conditions, and limit many health care consumers' abilities to make
important health care decisions. Another reason is due to individuals'
limited abilities to fully interpret and understand complex health
terminology and instructions. This could be further exacerbated by
different belief systems and adoption of methods for prevention and
treatment. Limited numeracy can also impede the ability to make
personal decisions related to risk, risk avoidance, and risk reduction.
For instance, to follow health care instructions, patients need to be
able to comprehend written and oral prescription instructions,
directions for self-care, and plans for follow-up tests and
appointments.
Specific Objectives
Researchers are strongly encouraged to review the general
illustrative examples of topics relevant to health literacy provided
below. Applications should address health promotion, prevention,
treatment, or management of diseases or health conditions, and/or the
improvement of health or health care outcomes. The research must
involve at least one of the following:
Health literacy, or one of its many components, as a key
outcome;
Health literacy as a key explanatory variable for some
other outcome;
Methodological or technological improvement to strengthen
research on health literacy; and/or
Prevention and/or intervention strategies that focus on
health-literacy.
Studies to develop, or evaluate, the readability or utility of
specific materials that are intended for single uses or single
audiences are not responsive to this program announcement unless these
investigations are integral to testing a significant research
hypothesis related to health literacy.
Approaches
A wide variety of research approaches are encouraged:
Basic research that investigates or describes the nature
of health literacy and the magnitude of health literacy problems;
Applied research addressing issues pertinent to health
literacy practices (e.g., systems level interventions) and research-in-
practice (e.g., active
[[Page 78577]]
potential end users participate as supportive research partners);
Develop theoretical models, refine research constructs,
improve methods and measurements, and establish causal relationships
(e.g., between low health literacy and lack of effective health
promotion);
Evaluation research that develops and tests the
effectiveness of interventions, or adapts and tests existing programs
(including those that are implemented by health care systems and
systems outside of health care), to reduce low health literacy and its
adverse consequences;
Secondary analyses of existing datasets as well as meta-
analytic studies; and
Multilevel, multidisciplinary, interdisciplinary, and
transdisciplinary research is encouraged, especially studies that
incorporate individual, family, community and societal mediators of
health literacy in childhood and adulthood, or state-of-the-art health
communication theory and knowledge.
For additional information about NCI health literacy research
contact: Sabra F. Woolley, Ph.D., Program Director, Health
Communication and Informatics Research Branch, National Cancer
Institute, 6130 Executive Blvd. Room 4084, Bethesda, Maryland 20892-
7365, Phone: 301-435-4589, Fax: 301-480-2087, E-mail:
Sabra.Woolley@nih.hhs.gov.
Tobacco Control Research
AI/ANs have been documented to have the highest smoking rate of any
major racial/ethnic group in the U.S. According to the 2005 National
Health Interview Survey of adults 18 and over, 32% of AI/AN are current
smokers, compared with 21.9% of non-Hispanic whites, 21.5% of non-
Hispanic blacks, 13.3% of Asians and 16.2% of Hispanics. Prevalence of
smoking is high among both men (37.5%) and women (26.8%).\(1)\ A
similar pattern can be seen among youth, where AI/AN youth have
substantially higher smoking prevalence (23.1%) than non-Hispanic
whites (14.9%), Hispanics (9.3%), non-Hispanic blacks (6.5%), and
Asians (4.3%), according to data from the National Survey on Drug Use
and Health. These data also show that non-smoking AI/AN youth
demonstrated higher susceptibility to experimenting with smoking than
most other racial/ethnic groups.\(2)\
At the same time, however, tobacco use patterns among the AI/AN
population are complex and can vary substantially among subgroups of
this population. Smoking rates among AI/ANs vary widely by region,
being highest in the northwestern United States, in Canada, and in
Alaska. Additionally, use of smokeless tobacco is higher among AI/AN
adults compared with other racial/ethnic groups. Some studies have
found particularly high rates of smokeless tobacco use (greater than
50%) among AN populations, including pregnant women, due to the use of
Iqmik, a traditional form of smokeless tobacco.\(3)\
Understanding tobacco use among Native American populations is also
complicated by the fact that tobacco has had a substantial role in
Native American culture and tradition. Historically, tobacco has been
used in medicinal and healing rituals and in ceremonial and religious
practices. It is important to distinguish the traditional, ceremonial
uses of tobacco, which are limited to specific occasions, from
addictive use of tobacco products. However, the relationship between
these different contexts of tobacco use and their impact on behavior
has not received sufficient scientific study.
Moreover, limited data are available on the effectiveness of
tobacco use cessation interventions targeted to AI/ANs. Preliminary
focus group studies suggest that Native American smokers are more
likely to have negative attitudes towards pharmacotherapies, such as
concerns about side effects and lack of trust in conventional
medicine.\(4)\ Thus, there is a need to develop culturally-appropriate
interventions targeted to this population.
The NCI Tobacco Control Research Branch is committed to supporting
transdisciplinary research aimed at reducing disparities in tobacco use
and related health outcomes. The NARCH provides a unique mechanism to
support collaborative research involving researchers from multiple
disciplines to address a complex scientific and public health
challenge.
Sample research areas of interest include but are not limited to
the following:
Studies to understand the role of a range of behavioral,
cultural, and environmental factors that lead to initiation of tobacco
use among AI/AN populations;
Development and evaluation of culturally appropriate
interventions for tobacco use prevention and cessation targeted to AI/
AN populations;
Studies of how tobacco related attitudes and behaviors in
youth and adults are influenced by ceremonial tobacco use and other
cultural factors;
Studies of tobacco use behavior in relation to different
products, including dual use of cigarettes and smokeless tobacco;
Research on the characteristics, use, and health effects
of traditional tobacco products, such as Iqmik;
Research to understand disparities in tobacco use within
AI/AN populations given substantial variations by region and other
factors; and
Studies to identify and address barriers to treatment
among AI/ANs.
References
1. Tobacco Use Among Adults--United States, 2005. MMWR. October
27, 2006; 55: 1145-1148.
2. Racial/Ethnic Differences Among Youths in Cigarette Smoking
and Susceptibility to Start Smoking--United States, 2002-2004. MMWR.
December 1, 2006; 55; 1275-1277.
3. Renner CC, Patten CA, Day GE, Enoch CC, Schroeder DR, Offord
KP, Hurt RD, Gasheen A, Gill L. Tobacco use during pregnancy among
Alaska Natives in western Alaska. Alaska Med. 2005;47:12-16.
4. Burgess D, Fu SS, Joseph AM, Hatsukami DK, Solomon J, van Ryn
M. Beliefs and experiences regarding smoking cessation among
American Indians. Nicotine Tob Res. 2007;9 Suppl 1:S19-28.
For additional information about NCI tobacco research contact: Mark
Parascandola, PhD, Epidemiologist, Tobacco Control Research Branch,
National Cancer Institute, 6130 Executive Blvd. MSC 7337, Executive
Plaza North, Room 4039, Bethesda, MD 20892, Phone: 301-451-4587, Fax:
301-496-8675, E-mail: paramark@mail.nih.gov.
National Heart, Lung, and Blood Institute (NHLBI)
Cardiovascular and Respiratory Research
The NHLBI has a strong history of supporting research to document
and intervene on health disparities among AI/ANs, including the Strong
Heart Study, Pathways, Genetics of Coronary Artery Disease in Alaska
Natives (GOCADAN), the Stop Atherosclerosis in Native Diabetics Study
(SANDS), and Community-Responsive Interventions to Reduce
Cardiovascular Risk in AI/ANs.
The Strong Heart Study showed that many AI/AN communities bear a
heavy burden of cardiovascular disease (CVD) and cardiovascular risk
factors (e.g., obesity, diabetes) that could be reduced through
effective interventions on modifiable risk factors. The high burden of
disease will worsen unless behaviors and lifestyles affecting CVD risk
can be changed. Prevalence of obesity in AI/AN communities is about 50%
higher than in the U.S. general population, in which obesity is often
described as being of epidemic proportions. In some AI/AN communities,
cigarette smoking,
[[Page 78578]]
sedentary lifestyle, and stress augment the adverse effects of obesity.
AI/ANs are particularly vulnerable to Type 2 diabetes, a problem
exacerbated by high rates of obesity. Diabetes prevalence is 3-20 fold
higher among AI/ANs than in the general U.S. population. It is an
important cause of coronary heart disease, cardiomyopathy, end-stage
renal disease, non-traumatic amputation, and vision impairment. Lipid
abnormalities also are common in Type 2 diabetics, particularly high
triglycerides and low HDL-cholesterol levels. Dyslipidemia and blood
pressure can be improved by appropriate changes in diet and by
increased exercise. CVD risk is also substantially improved by smoking
cessation. In addition, attention to high stress levels, untreated
sleep disordered breathing, short sleep duration, and depression may be
warranted, because of evidence that they may influence the health
behaviors of interest. For example, poorer diet, higher smoking rates,
and physical inactivity are more prominent in those with high stress,
sleep disorders, or depression. These psychosocial factors also are
associated with CVD progression in observational epidemiologic studies,
and there is evidence from smaller clinical studies that they may
affect mechanisms leading to CVD. NHLBI is interested in supporting
research in AI/AN communities that promotes the adoption of healthy
lifestyles and/or improves behaviors related to cardiovascular risk,
such as weight reduction, regular physical activity, and smoking
cessation. These behaviors and lifestyles are known to affect
biological cardiovascular risk factors, such as hypertension,
dyslipidemia, obesity, glucose intolerance, and diabetes. In addition,
control of these risk factors by guideline-based use of
antihypertensive, lipid lowering, and hypoglycemic drugs can reduce
their adverse consequences. However, these pharmacological
interventions are often suboptimally utilized in AI/AN communities. The
NHLBI is interested in reducing cardiovascular disease mortality and
morbidity in AI/AN, whether by lifestyle changes, drug interventions,
or combinations thereof.
Lifestyles characterized by sleeping less than 7 hours per night
are associated with increased risk of CVD, obesity, diabetes, and all-
cause mortality. Insufficient sleep and poor sleep quality is
associated with abnormalities in hypothalamic-pituitary axis function
and behavioral stress. Sleep deprivation compromises vigilance,
judgment, mood, emotional expression, and other aspects of cognition
increasing the risk of unstable patterns of behavior. The ability of
sleep deprivation to enhance the encoding and recall of emotional
(relative to neutral) memories may profoundly influence social
interactions and stress. Insufficient sleep is associated with an
increased risk of new onset substance abuse and relapse, and new onset
depression and relapse. Intervention studies to assess the efficacy of
improving sleep as part of a healthy lifestyle or assessing how
improving sleep disorders could improve CVD outcomes would be of
interest to NHLBI. Sleep disordered breathing appears to be 30-60% more
common among American Indians than other racial and ethnic groups.
Sudden infant death syndrome occurs 2.5 times more frequently in AI/AN
children than in white children, and 2.0 times more frequently than in
the U.S. population as a whole.
AI/AN also have been documented to exhibit high rates of chronic
respiratory disease. AI/AN adults have the highest asthma rate among
single-race groups. Recent evidence suggests that 11.6 percent of AI/AN
suffer from asthma. This is significantly higher than the national
average of 7.5 percent, and much higher than every other single racial
or ethnic group. Chronic obstructive pulmonary disease (COPD), which
includes emphysema and chronic bronchitis, is the sixth leading cause
of death from chronic disease for AI/AN men and the seventh leading
cause of death for women. AI/AN have the second highest rates of cystic
fibrosis following whites. One in 10,500 AI/AN has cystic fibrosis
compared with one in 3,200 whites. Pueblo Indians and Zuni Indians have
higher incidence than among other AI/AN Tribes. NHLBI is interested in
supporting research in AI/AN communities that includes studies of
approaches to improve clinical delivery of efficacious treatments of
chronic lung disease and their risk factors, improved methods of
chronic lung disease self-management, studies to promote or maintain
respiratory health or improved methods of rehabilitation for diseases
of the lungs and airways, such as asthma, COPD, cystic fibrosis; sleep
disordered breathing, occupational lung diseases, pulmonary vascular
disease or pulmonary complications of AIDS.
In addition to these areas of research, the NHLBI recognizes a
unique and compelling need to promote diversity in the biomedical,
behavioral, clinical, and social sciences research workforce. The NHLBI
expects eff