Proposed Data Collection Submitted for Public Comment and Recommendations, 24007-24008 [2024-07288]
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Federal Register / Vol. 89, No. 67 / Friday, April 5, 2024 / Notices
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. 2024–07289 Filed 4–4–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–24–24EG; Docket No. CDC–2024–
0024]
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 Documenting
outcomes associated with Persistent Tic
Disorders (including Tourette
Syndrome) in Children, Adolescents,
and Young Adults through Surveillance.
This study will collect data on the
public health impact of persistent tic
disorders from children and adolescents
with tic disorders and their parents, as
well as young adults with tic disorders.
DATES: CDC must receive written
comments on or before June 4, 2024.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2024–
0024 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.
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SUMMARY:
VerDate Sep<11>2014
16:44 Apr 04, 2024
Jkt 262001
Please note: Submit all comments through
the Federal eRulemaking portal
(www.regulations.gov) or by U.S. mail to the
address listed above.
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.
FOR FURTHER INFORMATION CONTACT:
Proposed Project
Documenting outcomes associated
with Persistent Tic Disorders (including
PO 00000
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Fmt 4703
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24007
Tourette Syndrome) in Children,
Adolescents, and Young Adults through
Surveillance—New—National Center on
Birth Defects and Developmental
Disabilities (NCBDDD), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
There are an estimated 1.4 million
people in the U.S. affected by persistent
tic disorders (PTD), including Tourette
syndrome (TS). To support people with
these conditions, the impact of PTD/TS
must be understood. Although some
data on the impact of PTD/TS on social
relationships and education are
available, other potential outcomes
associated with PTD/TS have not been
well-documented; including associated
costs, suicidality, health care transition,
and the prevalence of co-occurring
disorders and how co-occurring
disorders modify these outcomes.
Limited data are available on how these
outcomes may differ among subpopulations (e.g., by sex, race/ethnicity,
age group, and geography [e.g., urban/
rural]).
This data collection aims to document
priority outcomes including costs (e.g.,
education level, employment,
healthcare beyond those available in
claims data), prevalence of suicidality
risk, transition to adult healthcare, and
the prevalence of co-occurring
conditions and how they modify these
outcomes among children and
adolescents (4–17 years) and young
adults (18–26 years) with PTD/TS. Data
will be collected once from a participant
(i.e., individuals with PTD/TS and/or
their caregiver), via a survey, and a
clinical assessment of tic symptoms. All
questions for the Tic Impact
Surveillance Survey, the survey created
for this surveillance project, were
selected from national surveys or
previously validated measures. This
will allow us to compare estimates from
the Tic Impact Surveillance Survey to
external prevalence estimates for the
same health indicators in US children,
adolescents, and young adults in the
general population and to previously
published findings. Data will be used to
inform where resources for families and
healthcare providers (e.g., professional
trainings) are most needed to support
people with PTD/TS and their families
and to address health inequities among
the population.
CDC requests OMB approval for an
estimated 401 annual burden hours.
There is no cost to respondents other
than their time to participate.
E:\FR\FM\05APN1.SGM
05APN1
24008
Federal Register / Vol. 89, No. 67 / Friday, April 5, 2024 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Number of
respondents
Total burden
(in hours)
Form name
Parents of children 4–17 years with a persistent tic disorder.
Children 4–8 years with a persistent tic disorder.
Children 9–11 years with a persistent tic
disorder.
Adolescents (teens) 12–17 years with a persistent tic disorder.
Adults (18–26 years) with a persistent tic
disorder.
Parent ...................................
225
1
45/60
169
Child 4–8 ..............................
30
1
20/60
10
Child 9–11 ............................
45
1
45/60
34
Adolescent ............................
150
1
45/60
113
Adult ......................................
75
1
1
75
Total .......................................................
...............................................
........................
........................
........................
401
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. 2024–07288 Filed 4–4–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Operating Officer, Centers for Disease
Control and Prevention, has been
delegated the authority to sign Federal
Register notices pertaining to
announcements of meetings and other
committee management activities, for
both the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Kalwant Smagh,
Director, Office of Strategic Business
Initiatives, Office of the Chief Operating
Officer, Centers for Disease Control and
Prevention.
Centers for Disease Control and
Prevention
Advisory Board on Radiation and
Worker Health
[FR Doc. 2024–07301 Filed 4–4–24; 8:45 am]
BILLING CODE 4163–18–P
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice of charter renewal.
AGENCY:
The Centers for Disease
Control and Prevention (CDC), within
the Department of Health and Human
Services (HHS), announces the renewal
of the charter of the Advisory Board on
Radiation and Worker Health (ABRWH).
FOR FURTHER INFORMATION CONTACT:
Rashaun Roberts, Ph.D., Designated
Federal Officer, Advisory Board on
Radiation and Worker Health, Centers
for Disease Control and Prevention,
Department of Health and Human
Services, 1090 Tusculum Avenue,
Mailstop C–24, Cincinnati, Ohio 45226.
Telephone: (513) 533–6800; Email:
ocas@cdc.gov.
SUPPLEMENTARY INFORMATION: CDC is
providing notice under 5 U.S.C. 1001–
1014 of the renewal of the charter of the
Advisory Board on Radiation and
Worker Health, Centers for Disease
Control and Prevention, Department of
Health and Human Services. This
charter has been renewed for a two-year
period through March 22, 2026.
The Director, Office of Strategic
Business Initiatives, Office of the Chief
SUMMARY:
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Average
burden per
response
(in hours)
Type of respondents
VerDate Sep<11>2014
16:44 Apr 04, 2024
Jkt 262001
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–10545, CMS–
R–246, CMS–43 and CMS–10842]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
AGENCY:
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995
(PRA), Federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information (including each proposed
extension or reinstatement of an existing
collection of information) and to allow
60 days for public comment on the
proposed action. Interested persons are
SUMMARY:
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Fmt 4703
Sfmt 4703
invited to send comments regarding our
burden estimates or any other aspect of
this collection of information, including
the necessity and utility of the proposed
information collection for the proper
performance of the agency’s functions,
the accuracy of the estimated burden,
ways to enhance the quality, utility, and
clarity of the information to be
collected, and the use of automated
collection techniques or other forms of
information technology to minimize the
information collection burden.
DATES: Comments must be received by
June 4, 2024.
ADDRESSES: When commenting, please
reference the document identifier or
OMB control number. To be assured
consideration, comments and
recommendations must be submitted in
any one of the following ways:
1. Electronically. You may send your
comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) that are accepting
comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number: ll, Room C4–26–05,
7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, please access the CMS PRA
website by copying and pasting the
following web address into your web
browser: https://www.cms.gov/
Regulations-and-Guidance/Legislation/
PaperworkReductionActof1995/PRAListing.
E:\FR\FM\05APN1.SGM
05APN1
]]>Agencies
[Federal Register Volume 89, Number 67 (Friday, April 5, 2024)]
[Notices]
[Pages 24007-24008]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-07288]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-24-24EG; Docket No. CDC-2024-0024]
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 Documenting outcomes associated with Persistent Tic Disorders
(including Tourette Syndrome) in Children, Adolescents, and Young
Adults through Surveillance. This study will collect data on the public
health impact of persistent tic disorders from children and adolescents
with tic disorders and their parents, as well as young adults with tic
disorders.
DATES: CDC must receive written comments on or before June 4, 2024.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2024-
0024 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
Documenting outcomes associated with Persistent Tic Disorders
(including Tourette Syndrome) in Children, Adolescents, and Young
Adults through Surveillance--New--National Center on Birth Defects and
Developmental Disabilities (NCBDDD), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
There are an estimated 1.4 million people in the U.S. affected by
persistent tic disorders (PTD), including Tourette syndrome (TS). To
support people with these conditions, the impact of PTD/TS must be
understood. Although some data on the impact of PTD/TS on social
relationships and education are available, other potential outcomes
associated with PTD/TS have not been well-documented; including
associated costs, suicidality, health care transition, and the
prevalence of co-occurring disorders and how co-occurring disorders
modify these outcomes. Limited data are available on how these outcomes
may differ among sub-populations (e.g., by sex, race/ethnicity, age
group, and geography [e.g., urban/rural]).
This data collection aims to document priority outcomes including
costs (e.g., education level, employment, healthcare beyond those
available in claims data), prevalence of suicidality risk, transition
to adult healthcare, and the prevalence of co-occurring conditions and
how they modify these outcomes among children and adolescents (4-17
years) and young adults (18-26 years) with PTD/TS. Data will be
collected once from a participant (i.e., individuals with PTD/TS and/or
their caregiver), via a survey, and a clinical assessment of tic
symptoms. All questions for the Tic Impact Surveillance Survey, the
survey created for this surveillance project, were selected from
national surveys or previously validated measures. This will allow us
to compare estimates from the Tic Impact Surveillance Survey to
external prevalence estimates for the same health indicators in US
children, adolescents, and young adults in the general population and
to previously published findings. Data will be used to inform where
resources for families and healthcare providers (e.g., professional
trainings) are most needed to support people with PTD/TS and their
families and to address health inequities among the population.
CDC requests OMB approval for an estimated 401 annual burden hours.
There is no cost to respondents other than their time to participate.
[[Page 24008]]
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)
----------------------------------------------------------------------------------------------------------------
Parents of children 4-17 years Parent.......... 225 1 45/60 169
with a persistent tic
disorder.
Children 4-8 years with a Child 4-8....... 30 1 20/60 10
persistent tic disorder.
Children 9-11 years with a Child 9-11...... 45 1 45/60 34
persistent tic disorder.
Adolescents (teens) 12-17 Adolescent...... 150 1 45/60 113
years with a persistent tic
disorder.
Adults (18-26 years) with a Adult........... 75 1 1 75
persistent tic disorder.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 401
----------------------------------------------------------------------------------------------------------------
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. 2024-07288 Filed 4-4-24; 8:45 am]
BILLING CODE 4163-18-P
