Proposed Data Collection Submitted for Public Comment and Recommendations, 71362-71363 [2023-22778]
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Federal Register / Vol. 88, No. 198 / Monday, October 16, 2023 / Notices
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[FR Doc. 2023–22575 Filed 10–13–23; 8:45 am]
BILLING CODE 4160–90–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–24–24AA; Docket No. CDC–2023–
0083]
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 effort to reduce public
burden and maximize the utility of
government information, invites the
general public and other Federal
agencies the opportunity to comment on
a proposed information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection project titled Rape Prevention
and Education (RPE) Program. The RPE
Program is designed to assess how
recipients are improving prevention
infrastructure, implementing, and
evaluating prevention strategies to
expand efforts to prevent sexual assault,
and using data to inform prevention
action.
DATES: CDC must receive written
comments on or before December 15,
2023.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2023–
0083 by either of the following methods:
• Federal eRulemaking Portal:
www.regulations.gov. Follow the
instructions for submitting comments.
• Mail: Jeffrey M. Zirger, Information
Collection Review Office, Centers for
Disease Control and Prevention, 1600
ddrumheller on DSK120RN23PROD with NOTICES1
SUMMARY:
VerDate Sep<11>2014
17:03 Oct 13, 2023
Jkt 262001
Clifton Road NE, MS H21–8, Atlanta,
Georgia 30329.
Instructions: All submissions received
must include the agency name and
Docket Number. CDC will post, without
change, all relevant comments to
www.regulations.gov.
Please note: Submit all comments
through the Federal eRulemaking portal
(www.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 Jeffrey M. Zirger,
Information Collection Review Office,
Centers for Disease Control and
Prevention, 1600 Clifton Road NE, MS
H21–8, Atlanta, Georgia 30329;
Telephone: 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 the OMB for approval. To
comply with this requirement, we are
publishing this notice of a proposed
data collection as described below.
The OMB is particularly interested in
comments that will help:
1. Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information will have
practical utility;
2. Evaluate the accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and
clarity of the information to be
collected;
4. Minimize the burden of the
collection of information on those who
are to respond, including through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submissions
of responses; and
5. Assess information collection costs.
PO 00000
Frm 00030
Fmt 4703
Sfmt 4703
Proposed Project
Rape Prevention and Education (RPE)
Program—New—National Center for
Injury Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Sexual violence (SV) is a major public
health problem, one in three women
and one in four men experienced sexual
violence involving physical contact
during their lifetimes. Nearly one in five
women and one in 38 men have
experienced completed or attempted
rape. Sexual violence starts early: one in
three female and one in four male rape
victims experienced it for the first time
between 11–17 years old. The Rape
Prevention and Education Program
(RPE) provides funding to health
departments and sexual violence
coalitions in all 50 States, the District of
Columbia (DC), and U.S. Territories, as
well as up to 10 Tribal coalitions. CDC
will collect data from RPE Program
recipients to assess how recipients are
improving prevention infrastructure,
implementing, and evaluating
prevention strategies to expand efforts
to prevent sexual assault, and using data
to inform prevention action.
Recipients will have an opportunity
to: (1) continue to build program and
partner capacity to facilitate and
monitor the implementation of SV
prevention programs, practices, and
policies; (2) continue to support State
and Territorial health departments’
implementation of community-and
societal-level programs, practices, and
policies to prevent SV; (3) continue to
support the implementation of datadriven, comprehensive, evidence-based
SV primary prevention strategies, and
approaches focused mainly on health
equity; and (4) continuously conduct
data to action activities to inform
changes or adaptations to existing SV
strategies or on selected and
implemented additional strategies.
RPE Program recipients or designated
delegates will submit data annually into
an online data system. Recipients will
monitor and report progress on their
goals, objectives, and activities, as well
as relevant information on the
implementation of their prevention
strategies, outcomes, evaluation, and
State action plan. Information will be
collected via online web-based survey
software. Descriptive analyses (e.g.,
frequencies and crosstabs) will be
performed on numeric or categorical
data, and content analyses (e.g.,
categorization) on open-ended or text
data. Information to be collected will
provide crucial data for program
E:\FR\FM\16OCN1.SGM
16OCN1
71363
Federal Register / Vol. 88, No. 198 / Monday, October 16, 2023 / Notices
performance monitoring and provide
CDC with the capacity to respond in a
timely manner to requests for
information about the program from the
Department of Health and Human
Services (HHS), the White House,
Congress, and other sources.
Information to be collected will also
strengthen CDC’s ability to monitor
awardee progress, provide data-driven
technical assistance, and disseminate
the most current surveillance data on
unintentional and intentional injuries.
CDC requests OMB approval for an
estimated 1,408 annualized burden
hours. There are no direct costs to
respondents other than their time to
participate.
ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden
per response
(in hours)
Total burden
(in hours)
Form name
RPE-funded Health Departments (State,
DC, and Territories), Sexual Assault Coalitions, Tribal Coalitions, and their Designated Delegates.
Annual Performance Report
Program Director Survey ......
Lead Evaluator Survey .........
128
128
128
1
1
1
10
30/60
30/60
1280
64
64
Total .......................................................
...............................................
........................
........................
........................
1408
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2023–22778 Filed 10–13–23; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–24–1333]
Agency Forms Undergoing Paperwork
Reduction Act Review
ddrumheller on DSK120RN23PROD with NOTICES1
Number of
responses per
respondent
Number of
respondents
Type of respondents
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled ‘‘Feeding My
Baby and Me: Infant Feeding Practices
Study III (FMB&M–IFPS III)’’ to the
Office of Management and Budget
(OMB) for review and approval. CDC
previously published a ‘‘Proposed Data
Collection Submitted for Public
Comment and Recommendations’’
notice on June 9, 2023 to obtain
comments from the public and affected
agencies. CDC received three comments
related to the previous notice. This
notice serves to allow an additional 30
days for public and affected agency
comments.
CDC will accept all comments for this
proposed information collection project.
The Office of Management and Budget
is particularly interested in comments
that:
(a) Evaluate whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
VerDate Sep<11>2014
17:03 Oct 13, 2023
Jkt 262001
whether the information will have
practical utility;
(b) Evaluate the accuracy of the
agencies estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used;
(c) Enhance the quality, utility, and
clarity of the information to be
collected;
(d) Minimize the burden of the
collection of information on those who
are to respond, including, through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses; and
(e) Assess information collection
costs.
To request additional information on
the proposed project or to obtain a copy
of the information collection plan and
instruments, call (404) 639–7570.
Comments and recommendations for the
proposed information collection should
be sent within 30 days of publication of
this notice to www.reginfo.gov/public/
do/PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function. Direct written
comments and/or suggestions regarding
the items contained in this notice to the
Attention: CDC Desk Officer, Office of
Management and Budget, 725 17th
Street NW, Washington, DC 20503 or by
fax to (202) 395–5806. Provide written
comments within 30 days of notice
publication.
Proposed Project
Feeding My Baby and Me: Infant
Feeding Practices Study III (OMB
Control No. 0920–1333, Exp. 4/30/
PO 00000
Frm 00031
Fmt 4703
Sfmt 4703
2024)—Extension—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
A child’s first two years of life can
have profound impacts on their later
dietary behaviors and health outcomes.
Early feeding behaviors (e.g.,
breastfeeding, timing of complementary
food introduction, intake of different
foods and beverages such as fruits,
vegetables, sugar sweetened beverages,
and maternal and infant feeding styles)
can play a role in the establishment of
later dietary behaviors and may be
associated with health outcomes (e.g.,
risk of infections, obesity, and weight
gain). However, limited data is available
to track how prenatal and maternal
practices impact infant feeding and
health in the early years of life. Findings
from the Feeding My Baby and Me:
Infant Feeding Practices Study III
(FMB&M–IFPS III) will be used to fill
research gaps on how feeding behaviors,
patterns, and practices change over the
first two years of life and the healthrelated impacts; inform multiple Federal
agency efforts targeting maternal and
infant and toddler nutrition through
work in hospitals, with health care
providers, with early care and education
providers, and outreach to families and
caregivers; and provide context to
documents such as the U.S. Dietary
Guidelines for Americans, which will
include pregnant women and children
birth to 24 months of age for the first
time in 2020–2025.
CDC requests an Extension of an
existing information collection designed
to address current gaps in knowledge
and strengthen programmatic efforts
aimed at promoting optimal nutrition
and health in children less than two
E:\FR\FM\16OCN1.SGM
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]]>Agencies
[Federal Register Volume 88, Number 198 (Monday, October 16, 2023)]
[Notices]
[Pages 71362-71363]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-22778]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-24-24AA; Docket No. CDC-2023-0083]
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 effort to reduce public burden and maximize the
utility of government information, invites the general public and other
Federal agencies the opportunity to comment on a proposed information
collection, as required by the Paperwork Reduction Act of 1995. This
notice invites comment on a proposed information collection project
titled Rape Prevention and Education (RPE) Program. The RPE Program is
designed to assess how recipients are improving prevention
infrastructure, implementing, and evaluating prevention strategies to
expand efforts to prevent sexual assault, and using data to inform
prevention action.
DATES: CDC must receive written comments on or before December 15,
2023.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2023-
0083 by either of the following methods:
Federal eRulemaking Portal: www.regulations.gov. Follow
the instructions for submitting comments.
Mail: Jeffrey M. Zirger, Information Collection Review
Office, Centers for Disease Control and Prevention, 1600 Clifton Road
NE, MS H21-8, Atlanta, Georgia 30329.
Instructions: All submissions received must include the agency name
and Docket Number. CDC will post, without change, all relevant comments
to www.regulations.gov.
Please note: Submit all comments through the Federal eRulemaking
portal (www.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 Jeffrey M. Zirger, Information Collection
Review Office, Centers for Disease Control and Prevention, 1600 Clifton
Road NE, MS H21-8, Atlanta, Georgia 30329; Telephone: 404-639-7570;
Email: [email protected].
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 the OMB for approval. To
comply with this requirement, we are publishing this notice of a
proposed data collection as described below.
The OMB is particularly interested in comments that will help:
1. Evaluate whether the proposed collection of information is
necessary for the proper performance of the functions of the agency,
including whether the information will have practical utility;
2. Evaluate the accuracy of the agency's estimate of the burden of
the proposed collection of information, including the validity of the
methodology and assumptions used;
3. Enhance the quality, utility, and clarity of the information to
be collected;
4. Minimize the burden of the collection of information on those
who are to respond, including through the use of appropriate automated,
electronic, mechanical, or other technological collection techniques or
other forms of information technology, e.g., permitting electronic
submissions of responses; and
5. Assess information collection costs.
Proposed Project
Rape Prevention and Education (RPE) Program--New--National Center
for Injury Prevention and Control (NCIPC), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
Sexual violence (SV) is a major public health problem, one in three
women and one in four men experienced sexual violence involving
physical contact during their lifetimes. Nearly one in five women and
one in 38 men have experienced completed or attempted rape. Sexual
violence starts early: one in three female and one in four male rape
victims experienced it for the first time between 11-17 years old. The
Rape Prevention and Education Program (RPE) provides funding to health
departments and sexual violence coalitions in all 50 States, the
District of Columbia (DC), and U.S. Territories, as well as up to 10
Tribal coalitions. CDC will collect data from RPE Program recipients to
assess how recipients are improving prevention infrastructure,
implementing, and evaluating prevention strategies to expand efforts to
prevent sexual assault, and using data to inform prevention action.
Recipients will have an opportunity to: (1) continue to build
program and partner capacity to facilitate and monitor the
implementation of SV prevention programs, practices, and policies; (2)
continue to support State and Territorial health departments'
implementation of community-and societal-level programs, practices, and
policies to prevent SV; (3) continue to support the implementation of
data-driven, comprehensive, evidence-based SV primary prevention
strategies, and approaches focused mainly on health equity; and (4)
continuously conduct data to action activities to inform changes or
adaptations to existing SV strategies or on selected and implemented
additional strategies.
RPE Program recipients or designated delegates will submit data
annually into an online data system. Recipients will monitor and report
progress on their goals, objectives, and activities, as well as
relevant information on the implementation of their prevention
strategies, outcomes, evaluation, and State action plan. Information
will be collected via online web-based survey software. Descriptive
analyses (e.g., frequencies and crosstabs) will be performed on numeric
or categorical data, and content analyses (e.g., categorization) on
open-ended or text data. Information to be collected will provide
crucial data for program
[[Page 71363]]
performance monitoring and provide CDC with the capacity to respond in
a timely manner to requests for information about the program from the
Department of Health and Human Services (HHS), the White House,
Congress, and other sources. Information to be collected will also
strengthen CDC's ability to monitor awardee progress, provide data-
driven technical assistance, and disseminate the most current
surveillance data on unintentional and intentional injuries.
CDC requests OMB approval for an estimated 1,408 annualized burden
hours. There are no direct costs to respondents other than their time
to participate.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response Total burden
respondents respondent (in hours) (in hours)
----------------------------------------------------------------------------------------------------------------
RPE-funded Health Departments Annual 128 1 10 1280
(State, DC, and Territories), Performance 128 1 30/60 64
Sexual Assault Coalitions, Report. 128 1 30/60 64
Tribal Coalitions, and their Program Director
Designated Delegates. Survey.
Lead Evaluator
Survey.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 1408
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2023-22778 Filed 10-13-23; 8:45 am]
BILLING CODE 4163-18-P
