Proposed Data Collections Submitted for Public Comment and Recommendations, 13852-13853 [E6-3916]
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Federal Register / Vol. 71, No. 52 / Friday, March 17, 2006 / Notices
will be funded. It is strongly
recommended that statewide
collaborative efforts be forged with
organizations with experience working
with or representing the targeted
population.
2. Cost Sharing or Matching
Grantees are required to provide at
least 25 percent of the total program
costs from non-federal cash or in-kind
resources in order to be considered for
the award. In accordance with 48 U.S.C.
1469a (d), matching requirements are
waived for grantee applicants from
Guam and the U.S. Virgin Islands.
3. DUNS Number
The Office of Management and Budget
requires applicants to provide a Dun
and Bradstreet (D&B) Data Universal
Numbering System (DUNS) number
when applying for Federal grants or
cooperative agreements on or after
October 1, 2003. It is entered on the SF
424. It is a unique, nine-digit
identification number, which provides
unique identifiers of single business
entities. The D–U–N–S number is free
and easy to obtain.
Organizations can receive a DUNS
number at no cost by calling the
dedicated toll-free DUNS Number
request line at 1–866–705–5711 or by
using this link: https://
www.whitehouse.gov/omb/grants/
duns_num_guide.pdf.
sroberts on PROD1PC70 with NOTICES
4. Intergovernmental Review
Executive Order 12372,
Intergovernmental Review of Federal
Programs, is not applicable to these
grant applications.
IV. Application and Submission
Information
All applicants are required to submit
electronically through https://
www.grants.gov by midnight April 28,
2006.
Exceptions to this requirement may
only be made by the AoA grants
management officer, Stephen Daniels on
(202) 357–3464. Exceptions may only be
made to allow for catastrophic events
such as tornadoes, floods, etc.
Applicants are responsible for mailing
or hand delivering applications to AoA
in sufficient time to be received by 5:30
p.m. Eastern Time, April 28, 2006.
Please note AoA is requiring
applications for this announcement to
be submitted electronically through
https://www.grants.gov. The Grants.gov
registration process can take several
days. If your organization is not
currently registered with https://
www.grants.gov, please begin this
process immediately. For assistance
VerDate Aug<31>2005
16:52 Mar 16, 2006
Jkt 208001
with https://www.grants.gov, please
contact Arthur Miller at AoA’s
Grants.gov helpdesk at (202) 357–3438.
At https://www.grants.gov, you will be
able to download a copy of the
application packet, complete it off-line,
and then upload and submit the
application via the Grants.gov Web site.
Applicants unable to submit their
application via https://www.grants.gov
may request permission to submit a
hard copy from AoA Grants
Management Officer, Stephen Daniels,
(202) 357–3464,
Stephen.Daniels@aoa.hhs.gov.
1. Address for Application Submission
Hard copy submissions for which
approval has been requested and
received (per section IV(6) of the
announcement), may be mailed to the
U.S. Department of Health and Human
Services, Administration on Aging,
Office of Grants Management,
Washington, DC 20201, attn: Stephen
Daniels (HHS–2006–AoA–Initial–SM),
or hand-delivered (in person, via
messenger) to the U.S. Department of
Health and Human Services,
Administration on Aging, Office of
Grants Management, One Massachusetts
Avenue, NW., Room 4604, Washington,
DC 20001, attn: Stephen Daniels (HHS–
2006–AoA–SM–0603).
Applications not submitted
electronically must include one original
and two copies of the application.
Please include a stamped self addressed
postcard for acknowledgement of
receipt. Instructions for electronic
mailing of grant applications are
available at https://www.grants.gov/.
2. Submission Dates and Times
To receive consideration, applications
must be received by the deadline listed
in the DATES section of this Notice.
V. Responsiveness Criteria
Each application submitted will be
screened to determine whether it was
received by the closing date and time.
Applications received by the closing
date and time will be screened for
completeness and conformity with the
requirements outlined in Sections III
and IV of this Notice and the Program
Announcement. Only complete
applications that meet these
requirements will be reviewed and
evaluated competitively.
VI. Application Review Information
Eligible applications in response to
this announcement will be reviewed
according to the following evaluation
criteria: Purpose and Need for
Assistance (20 points); Approach, Work
Plan and Activities (30 points); Project
PO 00000
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Outcomes, Evaluation and
Dissemination (30 points); and Level of
Effort (20 points).
VII. Agency Contacts
Direct inquiries regarding
programmatic and grant issues to:
Project Officer: U.S. Department of
Health and Human Services,
Administration on Aging, Washington,
DC 20201. Attn: Barbara Lewis.
Telephone: (202) 357–3532, e-mail:
Barbara.Lewis@aoa.hhs.gov.
Grants Management Specialist: U.S.
Department of Health and Human
Services, Administration on Aging,
Washington, DC 20201. Attn: Stephen
Daniels. Telephone: (202) 357–3464, email: Stephen.Daniels@aoa.hhs.gov.
Dated: March 14, 2006.
Josefina G. Carbonell,
Assistant Secretary for Aging.
[FR Doc. E6–3932 Filed 3–16–06; 8:45 am]
BILLING CODE 4154–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–06–06AW]
Proposed Data Collections Submitted
for Public Comment and
Recommendations
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for
opportunity for public comment on
proposed data collection projects, the
Centers for Disease Control and
Prevention (CDC) will publish periodic
summaries of proposed projects. To
request more information on the
proposed projects or to obtain a copy of
the data collection plans and
instruments, call 404–639–5960 and
send comments to Seleda Perryman,
CDC Assistant Reports Clearance
Officer, 1600 Clifton Road, MS–D74,
Atlanta, GA 30333 or send an e-mail to
omb@cdc.gov.
Comments are invited on: (a) Whether
the proposed collection of information
is necessary for the proper performance
of the functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; and (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
E:\FR\FM\17MRN1.SGM
17MRN1
13853
Federal Register / Vol. 71, No. 52 / Friday, March 17, 2006 / Notices
or other forms of information
technology. Written comments should
be received within 60 days of this
notice.
Proposed Project
Supplement to the National Birth
Defects Prevention Study: Qualitative
Assessment of the Attitudes Mothers
Have Toward Collecting Biological
Specimens on their Infants and Young
Children to Study Risk Factors for Birth
Defects and Preterm Delivery—New—
National Center on Birth Defects and
Developmental Disabilities (NCBDDD),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
National Center on Birth Defects and
Developmental Disabilities (NCBDDD),
Centers for Disease Control and
Prevention (CDC), has been conducting
the National Birth Defects Prevention
Study (NBDPS) (OMB# 0920–0010)
since 1997. The NBDPS is a case-control
study of major birth defects that
includes cases identified from existing
birth defect surveillance registries in
nine states, including metropolitan
Atlanta. Control infants are randomly
selected from birth certificates or birth
hospital records. Mothers of case and
control infants are interviewed using a
computer-assisted telephone interview.
Parents are asked to collect cheek cells
from themselves and their infants for
DNA testing. Information gathered from
both the interviews and the DNA
specimens will be used to study
independent genetic and environmental
factors as well as gene-environment
interactions for a broad range of
carefully classified birth defects.
This proposed supplement to the
National Birth Defects Prevention Study
will use qualitative research to provide
data on the barriers to participation in
the collection of biological specimens
by mothers on themselves, their infants,
and young children. It is costly to
implement the collection of biological
specimens into an interview/
questionnaire-based study. However, an
ever-increasing number of studies
include the examination of
environmental and genetic interactions
to help medical and public health
professional’s better target appropriate
interventions. A critical component for
studies of gene variants is the collection
of biological specimens. Participation
and non-participation in the collection
of biological specimens is not fully
understood. We will conduct multiple
well-designed focus groups to assess the
attitudes of both mothers who
participated and mothers who did not
participate in the collection of biological
specimens to increase the effectiveness
of these studies. This information will
be useful to many groups at the CDC
who are currently collecting biological
specimens from infants and their
families but with less than optimal
response rates and those who are
working to implement studies that
include the use of biological specimens.
Scientists from the National Birth
Defects Prevention Study in NCBDDD,
the Pregnancy Risk Assessment
Monitoring System (PRAMS) in
National Center for Chronic Disease
Prevention and Health Promotion
(NCCDPHP), and Office of Genomics
and Disease Prevention (OGDP) have
received Collaborative Initiative
intramural funding to conduct focus
groups aimed at gaining insight into the
barriers and motivations women have
for participating in the collection of
biological specimens. Among the three
collaborating Centers within the
Coordinating Center for Health
Promotion, NCBDDD’s National Birth
Defects Prevention Study provides a
unique opportunity for exploring the
barriers and motivations toward
collection of genetic material. This focus
group project will recruit mothers who
participated in the maternal interview
for the NBDPS. There are no costs to the
respondents other than their time to
participate in the survey.
ESTIMATED ANNUALIZED BURDEN
Number of
respondents
Instrument
Telephone Contact ........................................................................................
Focus Group Discussion ...............................................................................
Dated: March 12, 2006.
Joan F. Karr,
Acting Reports Clearance Officer, Centers for
Disease Control and Prevention.
[FR Doc. E6–3916 Filed 3–16–06; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
sroberts on PROD1PC70 with NOTICES
Centers for Disease Control and
Prevention
Decision To Evaluate a Petition To
Designate a Class of Employees at the
Nevada Test Site, Mercury, Nevada, To
Be Included in the Special Exposure
Cohort
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
AGENCY:
VerDate Aug<31>2005
16:52 Mar 16, 2006
Jkt 208001
ACTION:
Frequency of
response
90
45
Notice.
SUMMARY: The Department of Health and
Human Services (HHS) gives notice as
required by 42 CFR 83.12(e) of a
decision to evaluate a petition to
designate a class of employees at the
Nevada Test Site, Mercury, Nevada, to
be included in the Special Exposure
Cohort under the Energy Employees
Occupational Illness Compensation
Program Act of 2000. The initial
proposed definition for the class being
evaluated, subject to revision as
warranted by the evaluation, is as
follows:
Facility: Nevada Test Site.
Location: Mercury, Nevada.
Job Titles and/or Job Duties: Workers
potentially exposed to above-ground
weapons testing.
Period of Employment: 1951 to 1963.
FOR FURTHER INFORMATION CONTACT:
Larry Elliott, Director, Office of
PO 00000
Frm 00048
Fmt 4703
Sfmt 4703
Average burden/response
(in hours)
Annual burden
hours
5/60
2
7.5
90
1
1
Compensation Analysis and Support,
National Institute for Occupational
Safety and Health, 4676 Columbia
Parkway, MS C–46, Cincinnati, OH
45226, Telephone 513–533–6800 (this is
not a toll-free number). Information
requests can also be submitted by e-mail
to OCAS@CDC.GOV.
Dated: March 10, 2006.
John Howard,
National Institute for Occupational Safety
and Health, Centers for Disease Control and
Prevention.
[FR Doc. 06–2588 Filed 3–16–06; 8:45 am]
BILLING CODE 4163–19–M
E:\FR\FM\17MRN1.SGM
17MRN1
]]>Agencies
[Federal Register Volume 71, Number 52 (Friday, March 17, 2006)]
[Notices]
[Pages 13852-13853]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: E6-3916]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-06-06AW]
Proposed Data Collections Submitted for Public Comment and
Recommendations
In compliance with the requirement of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for opportunity for public comment on
proposed data collection projects, the Centers for Disease Control and
Prevention (CDC) will publish periodic summaries of proposed projects.
To request more information on the proposed projects or to obtain a
copy of the data collection plans and instruments, call 404-639-5960
and send comments to Seleda Perryman, CDC Assistant Reports Clearance
Officer, 1600 Clifton Road, MS-D74, Atlanta, GA 30333 or send an e-mail
to omb@cdc.gov.
Comments are invited on: (a) Whether the proposed collection of
information is necessary for the proper performance of the functions of
the agency, including whether the information shall have practical
utility; (b) the accuracy of the agency's estimate of the burden of the
proposed collection of information; (c) ways to enhance the quality,
utility, and clarity of the information to be collected; and (d) ways
to minimize the burden of the collection of information on respondents,
including through the use of automated collection techniques
[[Page 13853]]
or other forms of information technology. Written comments should be
received within 60 days of this notice.
Proposed Project
Supplement to the National Birth Defects Prevention Study:
Qualitative Assessment of the Attitudes Mothers Have Toward Collecting
Biological Specimens on their Infants and Young Children to Study Risk
Factors for Birth Defects and Preterm Delivery--New--National Center on
Birth Defects and Developmental Disabilities (NCBDDD), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
National Center on Birth Defects and Developmental Disabilities
(NCBDDD), Centers for Disease Control and Prevention (CDC), has been
conducting the National Birth Defects Prevention Study (NBDPS)
(OMB 0920-0010) since 1997. The NBDPS is a case-control study
of major birth defects that includes cases identified from existing
birth defect surveillance registries in nine states, including
metropolitan Atlanta. Control infants are randomly selected from birth
certificates or birth hospital records. Mothers of case and control
infants are interviewed using a computer-assisted telephone interview.
Parents are asked to collect cheek cells from themselves and their
infants for DNA testing. Information gathered from both the interviews
and the DNA specimens will be used to study independent genetic and
environmental factors as well as gene-environment interactions for a
broad range of carefully classified birth defects.
This proposed supplement to the National Birth Defects Prevention
Study will use qualitative research to provide data on the barriers to
participation in the collection of biological specimens by mothers on
themselves, their infants, and young children. It is costly to
implement the collection of biological specimens into an interview/
questionnaire-based study. However, an ever-increasing number of
studies include the examination of environmental and genetic
interactions to help medical and public health professional's better
target appropriate interventions. A critical component for studies of
gene variants is the collection of biological specimens. Participation
and non-participation in the collection of biological specimens is not
fully understood. We will conduct multiple well-designed focus groups
to assess the attitudes of both mothers who participated and mothers
who did not participate in the collection of biological specimens to
increase the effectiveness of these studies. This information will be
useful to many groups at the CDC who are currently collecting
biological specimens from infants and their families but with less than
optimal response rates and those who are working to implement studies
that include the use of biological specimens.
Scientists from the National Birth Defects Prevention Study in
NCBDDD, the Pregnancy Risk Assessment Monitoring System (PRAMS) in
National Center for Chronic Disease Prevention and Health Promotion
(NCCDPHP), and Office of Genomics and Disease Prevention (OGDP) have
received Collaborative Initiative intramural funding to conduct focus
groups aimed at gaining insight into the barriers and motivations women
have for participating in the collection of biological specimens. Among
the three collaborating Centers within the Coordinating Center for
Health Promotion, NCBDDD's National Birth Defects Prevention Study
provides a unique opportunity for exploring the barriers and
motivations toward collection of genetic material. This focus group
project will recruit mothers who participated in the maternal interview
for the NBDPS. There are no costs to the respondents other than their
time to participate in the survey.
Estimated Annualized Burden
----------------------------------------------------------------------------------------------------------------
Average burden/
Instrument Number of Frequency of response (in Annual burden
respondents response hours) hours
----------------------------------------------------------------------------------------------------------------
Telephone Contact.............................. 90 1 5/60 7.5
Focus Group Discussion......................... 45 1 2 90
----------------------------------------------------------------------------------------------------------------
Dated: March 12, 2006.
Joan F. Karr,
Acting Reports Clearance Officer, Centers for Disease Control and
Prevention.
[FR Doc. E6-3916 Filed 3-16-06; 8:45 am]
BILLING CODE 4163-18-P
