Agency Forms Undergoing Paperwork Reduction Act Review, 101015-101016 [2024-29444]
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Federal Register / Vol. 89, No. 240 / Friday, December 13, 2024 / Notices
2. Monthly Reports
(a) Participant Report
(b) Investment Report
(c) Legislative Report
3. Quarterly Reports
(d) Vendor Risk Management
4. 2025 Board Calendar Review
Closed Session
5. Information covered under 5 U.S.C.
552b (c)(10).
Authority: 5 U.S.C. 552b (e)(1).
Dated: December 9, 2024.
Dharmesh Vashee,
General Counsel, Federal Retirement Thrift
Investment Board.
[FR Doc. 2024–29340 Filed 12–12–24; 8:45 am]
BILLING CODE P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–25–24GO]
khammond on DSK9W7S144PROD with NOTICES
Agency Forms Undergoing Paperwork
Reduction Act Review
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled ‘‘Formative
Research on Adverse and positive
childhood experiences, social
determinants of health, and health
equity among young adults in the US’’
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 July 19, 2024 to obtain
comments from the public and affected
agencies. CDC received 17 nonsubstantive 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
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;
VerDate Sep<11>2014
18:12 Dec 12, 2024
Jkt 265001
(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
Formative Research on Adverse and
Positive Childhood Experiences, Social
Determinants of Health, and Health
Equity Among Young Adults in the
US—New—National Center for Injury
Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
CDC requests OMB approval for a new
data collection titled Formative research
on adverse and positive childhood
experiences, social determinants of
health, and health equity among young
adults in the US. This study will help
CDC to better understand the
relationship between adverse childhood
experiences (ACEs), positive childhood
experiences (PCEs), social determinants
of health (SDOH), and health outcomes
among young adults from populations
that have been socially and
economically marginalized. This is a
group at high risk for experiencing
childhood adversity and has been
historically underrepresented in
research studies.
CDC is seeking approval from OMB to
conduct a one-time information
collection effort, with data collection
occurring over a 12-month period. The
PO 00000
Frm 00067
Fmt 4703
Sfmt 4703
101015
study will include 6,000 young adults
ages 18 to 24 living in the United States.
Primary data collection in English and
Spanish, via a probability-based web
panel survey, will obtain new data on
retrospective assessments of ACEs and
other potentially traumatic experiences,
PCEs, SDOHs, and health and violence
outcomes. Sampling frameworks will be
designed to ensure overrepresentation of
some populations that are
disproportionately impacted by ACEs as
well as underrepresented in research
and violence prevention programming,
including individuals with disabilities;
individuals from racial and ethnic
minority groups; and individuals who
identify as sexual or gender minority.
This project expands the existing
evidence base and addresses several
gaps in extant data collection systems in
the following three ways:
First, this study expands how ACEs
are measured. Traditional ACEs
research has measured eight to ten
highly interconnected, household-level
childhood stressors. These include
sexual abuse, physical abuse, emotional
abuse, emotional neglect, physical
neglect, witnessing intimate partner
violence, parent separation/divorce, and
living in a home with exposure to
mental illness, substance misuse, and
incarceration (hereafter referred to as
traditional ACEs). However, most ACE
research does not account for a wide
array of other potentially traumatic
experiences that can exist across all
levels of the social ecology, including
stressors that uniquely impact
populations that are socially and
economically marginalized (e.g., fear of
deportation; experiences of transphobia;
exposure to neighborhood or
community violence). These potentially
traumatic experiences may have an
additive or multiplicative effect on risk
for poor outcomes or may have a greater
effect on risk relative to the
conventional ACEs categories.
Second, this study will create a
diverse sample which is statistically
powered to answer questions on how to
prevent ACEs and mitigate the impact of
specific and cumulative ACE exposures
among communities that have been
traditionally socially and economically
marginalized. Most samples used in
prior surveillance and research studies
do not sufficiently oversample underrepresented communities to allow for
disaggregation of results by sub-group.
Thus, there is a need for data samples
that allow for disaggregated analysis and
results.
Third, this study will link individual
level data to community-level variables.
While ACEs are individual experiences,
they are influenced by the contexts in
E:\FR\FM\13DEN1.SGM
13DEN1
101016
Federal Register / Vol. 89, No. 240 / Friday, December 13, 2024 / Notices
which children and families live. SDOH
are the conditions in which people are
born, grow, live, work, and age that are
shaped by the distribution of money,
power, and resources. SDOH contribute
to health and social inequities for
groups with disparities in access to
money, power and resources. Many
existing ACE datasets involving
individual-level respondents cannot be
linked to community-level variables.
This formative study will link survey
data with publicly available data on
structural factors (e.g., minimum wage;
generosity of unemployment benefits)
via USPS zip code or other geographic
indicators.
CDC requests OMB approval for an
estimated 3591 annual burden hours.
There is no cost to respondents other
than their time to participate.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondent
Form name
18–24-year-old survey respondents ...................
Recruitment Email ..............................................
First Follow up Recruitment Email—non-panel
Web Survey—English ........................................
Web Survey—Spanish .......................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Public Health Ethics and
Regulations, Office of Science, Centers for
Disease Control and Prevention.
[FR Doc. 2024–29444 Filed 12–12–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–25–0556]
khammond on DSK9W7S144PROD with NOTICES
Agency Forms Undergoing Paperwork
Reduction Act Review
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled ‘‘Assisted
Reproductive Technology (ART)
Program Reporting System’’ 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 April 5, 2024 to obtain
comments from the public and affected
agencies. CDC received two 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
whether the information will have
practical utility;
VerDate Sep<11>2014
18:12 Dec 12, 2024
Jkt 265001
(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
Assisted Reproductive Technology
(ART) Program Reporting System (OMB
Control No. 0920–0556, Exp. 12/31/
2024)—Revision—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
PO 00000
Frm 00068
Fmt 4703
Sfmt 4703
Number of
respondents
Number of
responses per
respondent
5,908
5,907
5,700
300
1
5
1
1
Average
burden per
response
(in hours)
1/60
1/60
30/60
30/60
Background and Brief Description
Section 2(a) of Public Law 102–493
(known as the Fertility Clinic Success
Rate and Certification Act of 1992
(FCSRCA), 42 U.S.C. 263a–1(a)) requires
that each assisted reproductive
technology (ART) program shall
annually report to the Secretary through
the Centers for Disease Control and
Prevention: (1) pregnancy success rates
achieved by such ART program; and (2)
the identity of each embryo laboratory
used by such ART program and whether
the laboratory is certified or has applied
for such certification under the Act. The
required information is currently
reported by ART programs to CDC as
specified in the Assisted Reproductive
Technology (ART) Program Reporting
System (OMB Control No. 0920–0556,
Exp. 12/31/2024). CDC seeks to revise
burden hour estimates, modify data
elements collected, and to extend OMB
approval for a period of three years. The
revised total burden estimate is higher
than the previous approval, due to an
increase in the utilization of ART in the
United States and the number of
reported cycles. Data elements collected
will be modified to remove two data
elements no longer needed and add one
new data element to reflect current
clinical practice.
The estimated number of respondents
(ART programs or clinics) is 453, based
on the number of clinics that provided
information in 2021; the estimated
average number of responses (ART
cycles) per respondent is 913.
Additionally, approximately 5–10% of
responding clinics will be randomly
selected each year to participate in data
validation and quality control activities;
an estimated 35 clinics will be selected
to report validation data on 70 cycles
each on average. Finally, respondents
may provide feedback to CDC about the
usability and utility of the reporting
E:\FR\FM\13DEN1.SGM
13DEN1
]]>Agencies
[Federal Register Volume 89, Number 240 (Friday, December 13, 2024)]
[Notices]
[Pages 101015-101016]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-29444]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-25-24GO]
Agency Forms Undergoing Paperwork Reduction Act Review
In accordance with the Paperwork Reduction Act of 1995, the Centers
for Disease Control and Prevention (CDC) has submitted the information
collection request titled ``Formative Research on Adverse and positive
childhood experiences, social determinants of health, and health equity
among young adults in the US'' 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 July 19, 2024 to obtain comments from the public and affected
agencies. CDC received 17 non-substantive 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 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
Formative Research on Adverse and Positive Childhood Experiences,
Social Determinants of Health, and Health Equity Among Young Adults in
the US--New--National Center for Injury Prevention and Control (NCIPC),
Centers for Disease Control and Prevention (CDC).
Background and Brief Description
CDC requests OMB approval for a new data collection titled
Formative research on adverse and positive childhood experiences,
social determinants of health, and health equity among young adults in
the US. This study will help CDC to better understand the relationship
between adverse childhood experiences (ACEs), positive childhood
experiences (PCEs), social determinants of health (SDOH), and health
outcomes among young adults from populations that have been socially
and economically marginalized. This is a group at high risk for
experiencing childhood adversity and has been historically
underrepresented in research studies.
CDC is seeking approval from OMB to conduct a one-time information
collection effort, with data collection occurring over a 12-month
period. The study will include 6,000 young adults ages 18 to 24 living
in the United States. Primary data collection in English and Spanish,
via a probability-based web panel survey, will obtain new data on
retrospective assessments of ACEs and other potentially traumatic
experiences, PCEs, SDOHs, and health and violence outcomes. Sampling
frameworks will be designed to ensure overrepresentation of some
populations that are disproportionately impacted by ACEs as well as
underrepresented in research and violence prevention programming,
including individuals with disabilities; individuals from racial and
ethnic minority groups; and individuals who identify as sexual or
gender minority.
This project expands the existing evidence base and addresses
several gaps in extant data collection systems in the following three
ways:
First, this study expands how ACEs are measured. Traditional ACEs
research has measured eight to ten highly interconnected, household-
level childhood stressors. These include sexual abuse, physical abuse,
emotional abuse, emotional neglect, physical neglect, witnessing
intimate partner violence, parent separation/divorce, and living in a
home with exposure to mental illness, substance misuse, and
incarceration (hereafter referred to as traditional ACEs). However,
most ACE research does not account for a wide array of other
potentially traumatic experiences that can exist across all levels of
the social ecology, including stressors that uniquely impact
populations that are socially and economically marginalized (e.g., fear
of deportation; experiences of transphobia; exposure to neighborhood or
community violence). These potentially traumatic experiences may have
an additive or multiplicative effect on risk for poor outcomes or may
have a greater effect on risk relative to the conventional ACEs
categories.
Second, this study will create a diverse sample which is
statistically powered to answer questions on how to prevent ACEs and
mitigate the impact of specific and cumulative ACE exposures among
communities that have been traditionally socially and economically
marginalized. Most samples used in prior surveillance and research
studies do not sufficiently oversample under-represented communities to
allow for disaggregation of results by sub-group. Thus, there is a need
for data samples that allow for disaggregated analysis and results.
Third, this study will link individual level data to community-
level variables. While ACEs are individual experiences, they are
influenced by the contexts in
[[Page 101016]]
which children and families live. SDOH are the conditions in which
people are born, grow, live, work, and age that are shaped by the
distribution of money, power, and resources. SDOH contribute to health
and social inequities for groups with disparities in access to money,
power and resources. Many existing ACE datasets involving individual-
level respondents cannot be linked to community-level variables. This
formative study will link survey data with publicly available data on
structural factors (e.g., minimum wage; generosity of unemployment
benefits) via USPS zip code or other geographic indicators.
CDC requests OMB approval for an estimated 3591 annual burden
hours. There is no cost to respondents other than their time to
participate.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per
Type of respondent Form name respondents responses per response
respondent (in hours)
----------------------------------------------------------------------------------------------------------------
18-24-year-old survey respondents........ Recruitment Email.......... 5,908 1 1/60
First Follow up Recruitment 5,907 5 1/60
Email--non-panel.
Web Survey--English........ 5,700 1 30/60
Web Survey--Spanish........ 300 1 30/60
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Public Health
Ethics and Regulations, Office of Science, Centers for Disease Control
and Prevention.
[FR Doc. 2024-29444 Filed 12-12-24; 8:45 am]
BILLING CODE 4163-18-P
