Proposed Data Collection Submitted for Public Comment and Recommendations, 58739-58740 [2024-15968]
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Federal Register / Vol. 89, No. 139 / Friday, July 19, 2024 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–24–24GO; Docket No. CDC–2024–
0052]
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 Formative
Research on Adverse and positive
childhood experiences, social
determinants of health, and health
equity among young adults in the U.S.
This data collection is designed to allow
CDC to better understand the
relationship between childhood
experiences and health outcomes among
young adults from populations that have
been socially and economically
marginalized.
SUMMARY:
CDC must receive written
comments on or before September 17,
2024.
DATES:
You may submit comments,
identified by Docket No. CDC–2024–
0052 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,
ddrumheller on DSK120RN23PROD with NOTICES1
ADDRESSES:
VerDate Sep<11>2014
18:53 Jul 18, 2024
Jkt 262001
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.
Proposed Project
Formative Research on Adverse and
positive childhood experiences, social
determinants of health, and health
equity among young adults in the U.S.—
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 for the study titled
Formative research on adverse and
positive childhood experiences, social
determinants of health, and health
PO 00000
Frm 00037
Fmt 4703
Sfmt 4703
58739
equity among young adults in the U.S.
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 to conduct a
one-time information collection effort,
with data collection occurring over a 12month period. The study will include
6,000 young adults ages 18–24 living in
the U.S. Primary data collection, in
English and Spanish, via a probabilitybased 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 10 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
E:\FR\FM\19JYN1.SGM
19JYN1
58740
Federal Register / Vol. 89, No. 139 / Friday, July 19, 2024 / Notices
prevent ACEs and mitigate the impact of
specific and cumulative ACEs 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
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 ACEs 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 zip code or other geographic
indicators.
It is estimated that up to 6,000 young
adults will complete the one-time
questionnaire. On average, the webbased surveys are estimated to take 30
minutes to complete. These estimates
were informed by consultations with
individuals with lived experiences and
individuals who participated in
cognitive interviews. The study team
engaged three consultants with lived
experience across the three main areas
of interest (individuals with a disability,
individuals who identify as sexual and
gender minorities, and individuals who
identify as racial/ethnic minorities) to
inform the development and
administration of the instrument. The
study team also engaged up to nine
individuals, in cognitive testing to
ensure the relevance, validity, and
equitable nature of the survey
instrument. These cognitive interviews
were a key component for developing a
final draft of the instrument that
accurately and reliably reflects the
experiences and perspectives of a
diverse range of individuals, families,
and communities. Using a standard
estimated time for question completion,
the project team calculated the burden
by averaging the time to complete the
minimum and maximum number of
survey items a respondent could be
asked based on varying skip patterns.
The estimated annualized burden is
3,985 hours. There is no cost to
respondents other than their time to
participate.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total annual
burden
(in hours)
Form name
18–24-year-old Survey Respondents
Recruitment Email ............................
Follow up Recruitment Email—Nonpanel.
Web Survey—English ......................
Web Survey—Spanish .....................
5,908
5,907
1
1
5/60
5/60
493
492
5,700
300
1
1
30/60
30/60
2,850
150
...........................................................
........................
........................
........................
3,985
Total ...........................................
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. 2024–15968 Filed 7–18–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–24–24CB]
Agency Forms Undergoing Paperwork
Reduction Act Review
ddrumheller on DSK120RN23PROD with NOTICES1
Number of
respondents
Type of respondent
In accordance with the Paperwork
Reduction Act of 1995, the Centers for
Disease Control and Prevention (CDC)
has submitted the information
collection request titled ‘‘Evaluation of
an Online Prostate Cancer Decision
Aid’’ 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’’
VerDate Sep<11>2014
18:53 Jul 18, 2024
Jkt 262001
notice on January 26, 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;
(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
PO 00000
Frm 00038
Fmt 4703
Sfmt 4703
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.
E:\FR\FM\19JYN1.SGM
19JYN1
]]>Agencies
[Federal Register Volume 89, Number 139 (Friday, July 19, 2024)]
[Notices]
[Pages 58739-58740]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-15968]
[[Page 58739]]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-24-24GO; Docket No. CDC-2024-0052]
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 Formative Research on Adverse and positive childhood
experiences, social determinants of health, and health equity among
young adults in the U.S. This data collection is designed to allow CDC
to better understand the relationship between childhood experiences and
health outcomes among young adults from populations that have been
socially and economically marginalized.
DATES: CDC must receive written comments on or before September 17,
2024.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2024-
0052 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
Formative Research on Adverse and positive childhood experiences,
social determinants of health, and health equity among young adults in
the U.S.--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 for the study
titled Formative research on adverse and positive childhood
experiences, social determinants of health, and health equity among
young adults in the U.S. 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 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 18-24 living in
the U.S. 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 10 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
[[Page 58740]]
prevent ACEs and mitigate the impact of specific and cumulative ACEs
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 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 ACEs
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 zip code or other geographic
indicators.
It is estimated that up to 6,000 young adults will complete the
one-time questionnaire. On average, the web-based surveys are estimated
to take 30 minutes to complete. These estimates were informed by
consultations with individuals with lived experiences and individuals
who participated in cognitive interviews. The study team engaged three
consultants with lived experience across the three main areas of
interest (individuals with a disability, individuals who identify as
sexual and gender minorities, and individuals who identify as racial/
ethnic minorities) to inform the development and administration of the
instrument. The study team also engaged up to nine individuals, in
cognitive testing to ensure the relevance, validity, and equitable
nature of the survey instrument. These cognitive interviews were a key
component for developing a final draft of the instrument that
accurately and reliably reflects the experiences and perspectives of a
diverse range of individuals, families, and communities. Using a
standard estimated time for question completion, the project team
calculated the burden by averaging the time to complete the minimum and
maximum number of survey items a respondent could be asked based on
varying skip patterns. The estimated annualized burden is 3,985 hours.
There is no cost to respondents other than their time to participate.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total annual
Type of respondent Form name respondents responses per response (in burden (in
respondent hours) hours)
----------------------------------------------------------------------------------------------------------------
18-24-year-old Survey Recruitment 5,908 1 5/60 493
Respondents. Email.
Follow up 5,907 1 5/60 492
Recruitment
Email--Non-
panel.
Web Survey-- 5,700 1 30/60 2,850
English.
Web Survey-- 300 1 30/60 150
Spanish.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 3,985
----------------------------------------------------------------------------------------------------------------
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. 2024-15968 Filed 7-18-24; 8:45 am]
BILLING CODE 4163-18-P
