60 Day FRN

25287

Federal Register / Vol. 90, No. 114 / Monday, June 16, 2025 / Notices
smoke and e-cigarette aerosol exposure;
provision of school- and communitybased interventions, and cessation.
Results of the NYTS will continue to be
used to inform and evaluate the
National Comprehensive Tobacco
Control Program, provide data to inform
the Department of Health and Human

Service’s Tobacco Control Strategic
Action Plan, and provide national
benchmark data for state-level Youth
Tobacco Surveys. Information collected
through the NYTS also is expected to
provide multiple measures and data for
monitoring progress on seven tobacco-

related objectives for Healthy People
2030.
CDC requests OMB approval for three
years for an estimated annualized
burden of 22,600 hours. There are no
costs to respondents other than their
time to participate.

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent

Average
burden per
response
(in hours)

Total
burden
hours

Form name

State administrators ...........
District administrators ........
School administrators ........
Teachers ............................
Students .............................

State-level Recruitment Script for the NYTS ................
District-level Recruitment Script for the NYTS ..............
School-level Recruitment Script for the NYTS ..............
Data Collection Checklist ..............................................
National Youth Tobacco Survey ...................................
Screening for Cognitive Interviews ...............................
Cognitive Interviews ......................................................
Pilot Testing ...................................................................

42
384
546
1,365
28,704
300
30
100

1
1
1
1
1
1
2
1

30/60
30/60
30/60
15/60
45/60
10/60
120/60
45/60

21
192
273
341
21,528
50
120
75

Total ............................

........................................................................................

........................

........................

....................

22,600

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. 2025–10861 Filed 6–13–25; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–25–1092; Docket No. CDC–2025–
0019]

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 continuing information collection, as
required by the Paperwork Reduction
Act of 1995. This notice invites
comment on a proposed information
collection project titled Sudden Death
in the Young.
The goal of the Sudden Death in the
Young (SDY) data collection is to
improve and standardize ascertainment
of deaths so that funded jurisdictions

SUMMARY:

ddrumheller on DSK120RN23PROD with NOTICES1

Number of
respondents

Type of respondent

VerDate Sep<11>2014

18:38 Jun 13, 2025

Jkt 265001

can better understand the incidence and
risk factors for sudden death in youth.
DATES: CDC must receive written
comments on or before August 15, 2025.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2025–
0019 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: 404–639–7118; 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

PO 00000

Frm 00087

Fmt 4703

Sfmt 4703

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
Sudden Death in the Young (OMB
Control No. 0920–1092, Exp. 09/30/

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25288

Federal Register / Vol. 90, No. 114 / Monday, June 16, 2025 / Notices

2025)—Revision—National Center for
Chronic Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Estimates of the annual incidence of
Sudden Death in the Young (SDY) vary
broadly due to differences in case
definitions, inconsistencies in
classifying cause of death on death
certificates, study populations, and case
ascertainment. To address the need for
improved estimates of SDY incidence
and its epidemiology based on uniform
cases definitions, CDC, in collaboration
with NIH’s National Heart, Lung, and
Blood Institute (NHLBI) and National
Institute of Neurological Disorders and
Stroke (NINDS), implemented the SDY
Case Registry in 2015. To meet the

collect data on approximately 606 SDY
cases per year. Each of the 12 CDCfunded state/jurisdiction awardees will,
on average, review and enter data on 51
of 606 cases each year. Burden is
estimated for reporting required case
information. It is estimated that
approximately half (303) of the
estimated 606 SDY cases will undergo
advanced clinical review by a team of
three medical experts.
OMB approval is requested for three
years. The total estimated annual
burden is 438 hours which is a decrease
of 73 hours from the previously
approved information collection request
due to a decrease in the number of
participating states/local jurisdictions
from 13 to 12. There are no costs to
respondents other than their time.

ongoing need to produce accurate and
uniform information, CDC, and NIH
continued the SDY Case Registry in
2018 with 13 recipients through a CDCbased cooperative agreement program
(DP18–1806). In 2023, a new
cooperative agreement program began
with 12 recipients (DP23–0006) was
launched by CDC with continued
support from NIH. The current revision
seeks to revise burden hour estimates,
modify responses for data elements
collected, and to extend OMB approval
for a period of three years.
CDC recipients agree to compile a
defined set of SDY information about a
defined subset of child deaths through
the jurisdiction’s/state’s existing CDR
program. CDC estimates that the 12
participating states/jurisdictions will

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent

Average
burden per
response
(in hr)

Total burden
(in hr)

Form name

State Health Personnel .....................
Medical Expert ..................................
State Health Personnel .....................

SDY Module I ...................................
Advanced Review ............................
SDY Module N .................................

12
36
12

51
26
51

10/60
15/60
10/60

102
234
102

Total ...........................................

...........................................................

........................

........................

........................

438

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. 2025–10905 Filed 6–13–25; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–25–1368; Docket No. CDC–2025–
0014]

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:

ddrumheller on DSK120RN23PROD with NOTICES1

Number of
respondents

Type of respondent

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 continuing information collection, as
required by the Paperwork Reduction

SUMMARY:

VerDate Sep<11>2014

18:38 Jun 13, 2025

Jkt 265001

Act of 1995. This notice invites
comment on a proposed information
collection project titled Performance
Monitoring of CDC’s Comprehensive
Suicide Prevention Program. This
program will allow CDC to monitor
awardee’s progress, identify trends, and
translate and disseminate information
about successful suicide prevention and
control strategies.
DATES: CDC must receive written
comments on or before August 15, 2025.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2025–
0014 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

PO 00000

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Fmt 4703

Sfmt 4703

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

E:\FR\FM\16JNN1.SGM

16JNN1