Agency Forms Undergoing Paperwork Reduction Act Review, 71363-71364 [2023-22780]
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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
16OCN1
71364
Federal Register / Vol. 88, No. 198 / Monday, October 16, 2023 / Notices
years of age. FMB&M–IFPS III will be a
longitudinal study of pregnant women
and their new baby for two years.
Throughout the study planning period,
CDC engaged with subject matter
experts from multiple Federal agencies
including the National Institutes of
Health (NIH), the U.S. Department of
Agriculture (USDA), and the Food and
Drug Administration (FDA) to ensure
that FMB&M–IFPS III applies lessons
learned from previous studies and
represents the priorities and needs of
numerous stakeholders. The new study
design is based on updated
Form name
Pregnant/Postpartum Women .........................
Study Screener ..............................................
Study Consent ................................................
Prenatal Survey ..............................................
24-Hour Dietary Recall—Prenatal ..................
Replicate 24-Hour Dietary Recall—Prenatal
Request for notification of child’s birth ...........
Birth Screener ................................................
1-Month Survey ..............................................
2-Month Survey ..............................................
3-Month Survey ..............................................
24-Hour Dietary Recall—Month 3 ..................
Replicate 24-Hour Dietary Recall—Month 3 ..
4-Month Survey ..............................................
5-Month Survey ..............................................
6-Month Survey ..............................................
8-Month Survey ..............................................
10-Month Survey ............................................
12-Month Survey ............................................
15-Month Survey ............................................
18-Month Survey ............................................
21-Month Survey ............................................
24-Month Survey ............................................
[FR Doc. 2023–22780 Filed 10–13–23; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–24–1316; Docket No. CDC–2023–
0084]
Proposed Data Collection Submitted
for Public Comment and
Recommendations
The Centers for Disease
Control and Prevention (CDC), as part of
SUMMARY:
VerDate Sep<11>2014
17:03 Oct 13, 2023
Jkt 262001
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 continuing information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection project titled Aerosols from
Harmful Algal Blooms: Exposures and
Health Effects in Highly Exposed
Populations. The goal of this study is to
conduct exploratory analyses of the
relationships between HAB-related
biomonitoring data, environmental data,
and symptom reporting.
CDC must receive written
comments on or before December 15,
2023.
DATES:
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice with comment period.
AGENCY:
You may submit comments,
identified by Docket No. CDC–2023–
0084 by either of the following methods:
ADDRESSES:
PO 00000
Frm 00032
Fmt 4703
Sfmt 4703
recalls. CDC estimates that 7,477
pregnant women, ages 18–49, must be
screened in order to obtain complete
data on 2,500 study participants. The
goal is to recruit equal proportions of
non-Hispanic white, non-Hispanic
black, and Hispanic participants. An
OMB Extension is requested for one
year. CDC requests OMB approval for an
estimated 5,051 annualized burden
hours. Participation is voluntary, and
there are no costs to respondents other
than their time.
Estimated Annualized Burden Hours
Number of
respondents
Type of respondents
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
ddrumheller on DSK120RN23PROD with NOTICES1
methodology and questions, and
recruitment of a new cohort of study
participants.
CDC will collect information about
mother’s intentions, behaviors, feeding
decisions, and practices from pregnancy
through their child’s first two years of
life and how these change; child health
outcomes; and emerging issues related
to infant and toddler feeding practices.
Data will be collected using web-based
surveys at multiple time points. This
includes: (1) a prenatal survey; (2) 14
follow-up surveys after the baby is born;
and (3) 2–4 maternal dietary data
2,492
1,570
1,413
919
90
1,413
1,368
1,231
1,192
1,153
750
73
1,117
1,081
1,046
1,013
980
949
919
889
861
833
Number of
responses per
respondent
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
Average
burden per
response
(in hours)
3/60
5/60
20/60
24/60
24/60
2/60
2/60
20/60
15/60
15/60
24/60
24/60
15/60
15/60
15/60
15/60
20/60
15/60
15/60
15/60
15/60
15/60
• 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;
E:\FR\FM\16OCN1.SGM
16OCN1
]]>Agencies
[Federal Register Volume 88, Number 198 (Monday, October 16, 2023)]
[Notices]
[Pages 71363-71364]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-22780]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-24-1333]
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 ``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 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. 4/30/2024)--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 health-related 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
[[Page 71364]]
years of age. FMB&M-IFPS III will be a longitudinal study of pregnant
women and their new baby for two years. Throughout the study planning
period, CDC engaged with subject matter experts from multiple Federal
agencies including the National Institutes of Health (NIH), the U.S.
Department of Agriculture (USDA), and the Food and Drug Administration
(FDA) to ensure that FMB&M-IFPS III applies lessons learned from
previous studies and represents the priorities and needs of numerous
stakeholders. The new study design is based on updated methodology and
questions, and recruitment of a new cohort of study participants.
CDC will collect information about mother's intentions, behaviors,
feeding decisions, and practices from pregnancy through their child's
first two years of life and how these change; child health outcomes;
and emerging issues related to infant and toddler feeding practices.
Data will be collected using web-based surveys at multiple time points.
This includes: (1) a prenatal survey; (2) 14 follow-up surveys after
the baby is born; and (3) 2-4 maternal dietary data recalls. CDC
estimates that 7,477 pregnant women, ages 18-49, must be screened in
order to obtain complete data on 2,500 study participants. The goal is
to recruit equal proportions of non-Hispanic white, non-Hispanic black,
and Hispanic participants. An OMB Extension is requested for one year.
CDC requests OMB approval for an estimated 5,051 annualized burden
hours. Participation is voluntary, and there are no costs to
respondents other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Type of respondents Form name Number of responses per per response
respondents respondent (in hours)
----------------------------------------------------------------------------------------------------------------
Pregnant/Postpartum Women............. Study Screener.......... 2,492 1 3/60
Study Consent........... 1,570 1 5/60
Prenatal Survey......... 1,413 1 20/60
24-Hour Dietary Recall-- 919 1 24/60
Prenatal.
Replicate 24-Hour 90 1 24/60
Dietary Recall--
Prenatal.
Request for notification 1,413 1 2/60
of child's birth.
Birth Screener.......... 1,368 1 2/60
1-Month Survey.......... 1,231 1 20/60
2-Month Survey.......... 1,192 1 15/60
3-Month Survey.......... 1,153 1 15/60
24-Hour Dietary Recall-- 750 1 24/60
Month 3.
Replicate 24-Hour 73 1 24/60
Dietary Recall--Month 3.
4-Month Survey.......... 1,117 1 15/60
5-Month Survey.......... 1,081 1 15/60
6-Month Survey.......... 1,046 1 15/60
8-Month Survey.......... 1,013 1 15/60
10-Month Survey......... 980 1 20/60
12-Month Survey......... 949 1 15/60
15-Month Survey......... 919 1 15/60
18-Month Survey......... 889 1 15/60
21-Month Survey......... 861 1 15/60
24-Month Survey......... 833 1 15/60
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2023-22780 Filed 10-13-23; 8:45 am]
BILLING CODE 4163-18-P
