Proposed Data Collection Submitted for Public Comment and Recommendations, 11798-11800 [2016-04933]
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11798
Federal Register / Vol. 81, No. 44 / Monday, March 7, 2016 / Notices
within and across State Public Health
Actions 1305 funded programs.
The assessment is guided by three
process-related research questions and
multiple indicators designed to examine
changes in processes, organizational
structure, and capacity. It will also
examine states’ ability to implement a
coordinated approach across the
different chronic disease areas and the
four domains; challenges and benefits;
and measurable positive outcomes. The
research questions include: (1) What
changes did States make to create
greater synergy?, (2) To what extent
were redundancies reduced or
eliminated at the State level?, and (3)
How has coordination with critical
partners changed since the
implementation of State Public Health
Actions 1305?
from each funded program for a total of
approximately 408 respondents.
CDC will use survey findings to (1)
inform future CDC technical assistance
provision to State Public Health Actions
1305 funded programs, and (2) inform
future cross-cutting, coordinated
funding models. In addition, findings
will complement existing routine
reporting by gathering information
about the specific processes that support
program implementation plans.
Findings will be disseminated via
grantee webinars, grantee annual
meetings, reports to CDC leadership,
and U.S. Congressional reports.
OMB approval is requested for 2
years. Participation is voluntary and
respondents will not receive incentives
for participation. There are no costs to
respondents other than their time.
CDC plans to administer a web-based
survey to health departments receiving
funding through the State Public Health
Actions 1305 cooperative agreement,
including 50 states and the District of
Columbia. CDC plans to administer the
survey in 2016 (program year 4) and
2018 (program year 5) to explore
changes in partnerships and synergy
throughout the 5-year cooperative
agreement. Surveys will be
administered to health department staff
directly involved in planning and/or
implementation of the State Public
Health Actions 1305 program, including
principal investigators, chronic disease
directors, program evaluators,
epidemiologists, and program staff with
subject matter expertise in one or more
of the four categorical areas. CDC will
recruit approximately 8 individuals
ESTIMATED ANNUALIZED BURDEN HOURS
Type of
respondents
Principal Investigators .......................
Chronic Disease Directors ................
Program Evaluators ..........................
Epidemiologists .................................
Program Staff with Subject Matter
Expertise.
Total ...........................................
Grantee
Grantee
Grantee
Grantee
Grantee
1
1
1
1
1
45/60
45/60
45/60
45/60
45/60
38
38
38
38
153
...........................................................
........................
........................
........................
305
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60-Day–16–0987; Docket No. CDC–2016–
0023]
asabaliauskas on DSK3SPTVN1PROD with NOTICES
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing efforts to reduce public
burden and maximize the utility of
government information, invites the
SUMMARY:
18:37 Mar 04, 2016
Jkt 238001
Survey
Survey
Survey
Survey
Survey
Total
burden
(in hr)
51
51
51
51
204
[FR Doc. 2016–04938 Filed 3–4–16; 8:45 am]
Synergy
Synergy
Synergy
Synergy
Synergy
Average
burden per
response
(in hr)
Numberof
responses per
respondent
..................
..................
..................
..................
..................
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
VerDate Sep<11>2014
Number of
respondents
Form name
general public and other Federal
agencies to take this opportunity to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on the information collection
request Qualitative Information
Collection on Emerging Diseases among
the Foreign-born in the US that enables
CDC improve the planning and
implementation of disease prevention
and control strategies targeting
communicable diseases and other
emerging health issues among high-risk
foreign-born communities in specific
and limited geographic areas in the
United States where high numbers of
those populations live.
DATES: Written comments must be
received on or before May 6, 2016.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2016–
0023 by any of the following methods:
• Federal eRulemaking Portal:
Regulation.gov. Follow the instructions
for submitting comments.
• Mail: Leroy A. Richardson,
Information Collection Review Office,
Centers for Disease Control and
PO 00000
Frm 00061
Fmt 4703
Sfmt 4703
Prevention, 1600 Clifton Road NE., MS–
D74, Atlanta, Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. All relevant comments
received will be posted without change
to Regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
Regulations.gov.
Please note: All public comment should be
submitted through the Federal eRulemaking
portal (Regulations.gov) or by U.S. mail to the
address listed above.
To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact the Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE., MS–D74, Atlanta,
Georgia 30329; phone: 404–639–7570;
Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
FOR FURTHER INFORMATION CONTACT:
E:\FR\FM\07MRN1.SGM
07MRN1
11799
Federal Register / Vol. 81, No. 44 / Monday, March 7, 2016 / Notices
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
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; (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology; and (e) estimates of capital
or start-up costs and costs of operation,
maintenance, and purchase of services
to provide information. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, disclose or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
and systems for the purpose of
issues (e.g., tuberculosis, parasitic
diseases, lead poisoning, and mental
health issues) among foreign-born
populations in the United States.
Foreign-born populations are very
diverse in terms of countries of origin,
socio-demographic, cultural and
linguistic characteristics and geographic
destinations in the U.S. Data is
especially limited at the local level.
The purpose of the extension is to
continue efforts to improve the agency’s
understanding of the health status, risk
factors for disease, and other health
outcomes among foreign-born
individuals in the United States.
Numerous types of data will be
collected under the auspices of this
generic information collection. These
include, but are not limited to,
knowledge, attitudes, beliefs, behavioral
intentions, practices, behaviors, skills,
self-efficacy, and health information
needs and sources.
Under the terms of this generic, CDC
will employ focus groups and key
informant interviews to collect
information. Depending on the specific
purpose, the information collection may
be conducted either in-person, by
telephone, on paper, or online. For each
generic information collection, CDC will
submit to OMB the project summary
and information collection tools.
CDC requests a total of 1,025
respondents and 825 burden hours
annually. The respondents to these
information collections are foreign born
individuals in the United States. There
is no cost to respondents other than the
time required to provide the information
requested.
collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information; and to
transmit or otherwise disclose the
information.
Proposed Project
Qualitative Information Collection on
Emerging Diseases among the Foreignborn in the U.S. (0920–0987 expires 09/
30/2016)—Extension—Division of
Global Migration and Quarantine,
National Center for Emerging Zoonotic
and Infectious Diseases, Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC), National Center for
Emerging and Zoonotic Infectious
Diseases (NCEZID), Division of Global
Migration and Quarantine (DGMQ),
requests approval for an extension of the
current generic information collection
Qualitative Information Collection on
Emerging Diseases among the Foreignborn in the U.S.
This qualitative data collection is
needed by DGMQ because foreign-born
individuals are considered hard-toreach populations and are often missed
by routine information collection
systems in the United States. As a
consequence, limited information is
available about the health status,
knowledge, attitudes, health beliefs and
practices related to communicable
diseases and other emerging health
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Average
burden per
response
(in hours)
Number of
responses per
respondent
Total burden
hours
Type of respondent
Form name
Foreign-born from specific country of
birth in the United States.
Screeners for focus groups (assuming 2 screenings for each recruited
participant
in
focus
groups) (300 × 2 = 600).
Focus Groups (Approximately 30
focus groups/year and 10 participants per focus group).
Key informant interviews (Approximately 125 interviews/year).
600
1
10/60
100
300
1
2
600
125
1
1
125
...........................................................
........................
........................
........................
825
Foreign-born from specific country of
birth in the United States.
asabaliauskas on DSK3SPTVN1PROD with NOTICES
Foreign-born community leaders and
staff from organizations serving
those communities.
Total ...........................................
VerDate Sep<11>2014
18:37 Mar 04, 2016
Jkt 238001
PO 00000
Frm 00062
Fmt 4703
Sfmt 4703
E:\FR\FM\07MRN1.SGM
07MRN1
11800
Federal Register / Vol. 81, No. 44 / Monday, March 7, 2016 / Notices
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2016–04933 Filed 3–4–16; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–16–0984;Docket No. CDC–2016–
0025]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), as part of
its continuing efforts to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies to take this opportunity to
comment on proposed and/or
continuing information collections, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection entitled ‘‘DELTA FOCUS
Program Evaluation.’’ CDC will use the
information collected to improve the
national DELTA FOCUS program, and
to develop strategy interactions to help
the DELTA FOCUS program meet the
requirements of the Funding
Opportunity Announcement.
DATES: Written comments must be
received on or before May 6, 2016.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2016–
0025 by any of the following methods:
Federal eRulemaking Portal:
Regulation.gov. Follow the instructions
for submitting comments.
Mail: Leroy A. Richardson,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE., MS–
D74, Atlanta, Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. All relevant comments
received will be posted without change
to Regulations.gov, including any
personal information provided. For
access to the docket to read background
documents or comments received, go to
Regulations.gov.
asabaliauskas on DSK3SPTVN1PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
18:37 Mar 04, 2016
Jkt 238001
Please note: All public comment should be
submitted through the Federal eRulemaking
portal (Regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT:
To
request more information on the
proposed project or to obtain a copy of
the information collection plan and
instruments, contact the Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
Clifton Road NE., MS–D74, Atlanta,
Georgia 30329; phone: 404–639–7570;
Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
(44 U.S.C. 3501–3520), Federal agencies
must obtain approval from the Office of
Management and Budget (OMB) for each
collection of information they conduct
or sponsor. In addition, the PRA also
requires Federal agencies to provide a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each new
proposed collection, each proposed
extension of existing collection of
information, and each reinstatement of
previously approved information
collection before submitting the
collection to OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
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; (d) ways to minimize the
burden of the collection of information
on respondents, including through the
use of automated collection techniques
or other forms of information
technology; and (e) estimates of capital
or start-up costs and costs of operation,
maintenance, and purchase of services
to provide information. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, disclose or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
and systems for the purpose of
collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
PO 00000
Frm 00063
Fmt 4703
Sfmt 4703
the collection of information; and to
transmit or otherwise disclose the
information.
Proposed Project
DELTA FOCUS Program Evaluation—
Reinstatement with change—National
Center for Injury Prevention and Control
(NCIPC), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
Intimate Partner Violence (IPV) is a
serious, preventable public health
problem that affects millions of
Americans and results in serious
consequences for victims, families, and
communities. IPV occurs between two
people in a close relationship. The term
‘‘intimate partner’’ describes physical,
sexual, or psychological harm by a
current or former partner or spouse. IPV
can impact health in many ways,
including long-term health problems,
emotional impacts, and links to negative
health behaviors. IPV exists along a
continuum from a single episode of
violence to ongoing battering; many
victims do not report IPV to police,
friends, or family.
The purpose of the DELTA FOCUS
(Domestic Violence Prevention
Enhancement and Leadership Through
Alliances, Focusing on Outcomes for
Communities United with States)
program is to promote the prevention of
IPV through the implementation and
evaluation of strategies that create a
foundation for the development of
practice-based evidence. By
emphasizing primary prevention, this
program will support comprehensive
and coordinated approaches to IPV
prevention. Each State Domestic
Violence Coalition (SDVC) is required to
identify and fund one to two wellorganized, broad-based, active local
coalitions (referred to as coordinated
community responses or CCRs) that are
already engaging in, or are at capacity to
engage in, IPV primary prevention
strategies affecting the structural
determinants of health at the societal
and/or community levels of the social
ecological model. SDVCs must facilitate
and support local-level implementation
and hire empowerment evaluators to
support the evaluation of IPV
prevention strategies by the CCRs.
SDVCs must also implement and with
their empowerment evaluators, evaluate
state-level IPV prevention strategies.
CDC seeks a one-year OMB approval
to collect information electronically
from awardees, their CCRs and their
empowerment evaluators. Information
will be collected using the DELTA
FOCUS Program Evaluation Survey
(referred to as DF Survey). The DF
E:\FR\FM\07MRN1.SGM
07MRN1
]]>Agencies
[Federal Register Volume 81, Number 44 (Monday, March 7, 2016)]
[Notices]
[Pages 11798-11800]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-04933]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60-Day-16-0987; Docket No. CDC-2016-0023]
Proposed Data Collection Submitted for Public Comment and
Recommendations
AGENCY: Centers for Disease Control and Prevention (CDC), Department of
Health and Human Services (HHS).
ACTION: Notice with comment period.
-----------------------------------------------------------------------
SUMMARY: The Centers for Disease Control and Prevention (CDC), as part
of its continuing efforts to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies to take this opportunity to comment on proposed and/or
continuing information collections, as required by the Paperwork
Reduction Act of 1995. This notice invites comment on the information
collection request Qualitative Information Collection on Emerging
Diseases among the Foreign-born in the US that enables CDC improve the
planning and implementation of disease prevention and control
strategies targeting communicable diseases and other emerging health
issues among high-risk foreign-born communities in specific and limited
geographic areas in the United States where high numbers of those
populations live.
DATES: Written comments must be received on or before May 6, 2016.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2016-
0023 by any of the following methods:
Federal eRulemaking Portal: Regulation.gov. Follow the
instructions for submitting comments.
Mail: Leroy A. Richardson, Information Collection Review
Office, Centers for Disease Control and Prevention, 1600 Clifton Road
NE., MS-D74, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. All relevant comments received will be posted
without change to Regulations.gov, including any personal information
provided. For access to the docket to read background documents or
comments received, go to Regulations.gov.
Please note: All public comment should be submitted through the
Federal eRulemaking portal (Regulations.gov) or by U.S. mail to the
address listed above.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the information collection plan
and instruments, contact the Information Collection Review Office,
Centers for Disease Control and Prevention, 1600 Clifton Road NE., MS-
D74, Atlanta, Georgia 30329; phone: 404-639-7570; Email: omb@cdc.gov.
SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995
(PRA) (44 U.S.C. 3501-3520), Federal agencies must obtain approval from
the Office of Management and Budget (OMB) for each
[[Page 11799]]
collection of information they conduct or sponsor. In addition, the PRA
also requires Federal agencies to provide a 60-day notice in the
Federal Register concerning each proposed collection of information,
including each new proposed collection, each proposed extension of
existing collection of information, and each reinstatement of
previously approved information collection before submitting the
collection to OMB for approval. To comply with this requirement, we are
publishing this notice of a proposed data collection as described
below. 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; (d) ways to
minimize the burden of the collection of information on respondents,
including through the use of automated collection techniques or other
forms of information technology; and (e) estimates of capital or start-
up costs and costs of operation, maintenance, and purchase of services
to provide information. Burden means the total time, effort, or
financial resources expended by persons to generate, maintain, retain,
disclose or provide information to or for a Federal agency. This
includes the time needed to review instructions; to develop, acquire,
install and utilize technology and systems for the purpose of
collecting, validating and verifying information, processing and
maintaining information, and disclosing and providing information; to
train personnel and to be able to respond to a collection of
information, to search data sources, to complete and review the
collection of information; and to transmit or otherwise disclose the
information.
Proposed Project
Qualitative Information Collection on Emerging Diseases among the
Foreign-born in the U.S. (0920-0987 expires 09/30/2016)--Extension--
Division of Global Migration and Quarantine, National Center for
Emerging Zoonotic and Infectious Diseases, Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and Prevention (CDC), National
Center for Emerging and Zoonotic Infectious Diseases (NCEZID), Division
of Global Migration and Quarantine (DGMQ), requests approval for an
extension of the current generic information collection Qualitative
Information Collection on Emerging Diseases among the Foreign-born in
the U.S.
This qualitative data collection is needed by DGMQ because foreign-
born individuals are considered hard-to-reach populations and are often
missed by routine information collection systems in the United States.
As a consequence, limited information is available about the health
status, knowledge, attitudes, health beliefs and practices related to
communicable diseases and other emerging health issues (e.g.,
tuberculosis, parasitic diseases, lead poisoning, and mental health
issues) among foreign-born populations in the United States. Foreign-
born populations are very diverse in terms of countries of origin,
socio-demographic, cultural and linguistic characteristics and
geographic destinations in the U.S. Data is especially limited at the
local level.
The purpose of the extension is to continue efforts to improve the
agency's understanding of the health status, risk factors for disease,
and other health outcomes among foreign-born individuals in the United
States. Numerous types of data will be collected under the auspices of
this generic information collection. These include, but are not limited
to, knowledge, attitudes, beliefs, behavioral intentions, practices,
behaviors, skills, self-efficacy, and health information needs and
sources.
Under the terms of this generic, CDC will employ focus groups and
key informant interviews to collect information. Depending on the
specific purpose, the information collection may be conducted either
in-person, by telephone, on paper, or online. For each generic
information collection, CDC will submit to OMB the project summary and
information collection tools.
CDC requests a total of 1,025 respondents and 825 burden hours
annually. The respondents to these information collections are foreign
born individuals in the United States. There is no cost to respondents
other than the time required to provide the information requested.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Type of respondent Form name respondents responses per response (in hours
respondent hours)
----------------------------------------------------------------------------------------------------------------
Foreign-born from specific Screeners for 600 1 10/60 100
country of birth in the focus groups
United States. (assuming 2
screenings for
each recruited
participant in
focus groups)
(300 x 2 = 600).
Foreign-born from specific Focus Groups 300 1 2 600
country of birth in the (Approximately
United States. 30 focus groups/
year and 10
participants
per focus
group).
Foreign-born community leaders Key informant 125 1 1 125
and staff from organizations interviews
serving those communities. (Approximately
125 interviews/
year).
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 825
----------------------------------------------------------------------------------------------------------------
[[Page 11800]]
Leroy A. Richardson,
Chief, Information Collection Review Office, Office of Scientific
Integrity, Office of the Associate Director for Science, Office of the
Director, Centers for Disease Control and Prevention.
[FR Doc. 2016-04933 Filed 3-4-16; 8:45 am]
BILLING CODE 4163-18-P
