Proposed Data Collection Submitted for Public Comment and Recommendations, 38150-38151 [2024-09843]
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38150
Federal Register / Vol. 89, No. 89 / Tuesday, May 7, 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. 2024–09852 Filed 5–6–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–24–1355; Docket No. CDC–2024–
0022]
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 Evaluation of
the Division of Overdose Prevention
Technical Assistance Center. This data
collection allows CDC to collect
information from partner organizations
regarding feedback on their experiences
receiving technical assistance.
DATES: CDC must receive written
comments on or before July 8, 2024.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2024–
0022 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
khammond on DSKJM1Z7X2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
15:55 May 06, 2024
Jkt 262001
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.
Proposed Project
Evaluation of the Division of
Overdose Prevention Technical
Assistance Center (OMB Control No.,
0920–1355, Exp. 11/30/202)—
Revision—National Center for Injury
Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and
Prevention (CDC) is submitting a
Revision request for the currently
PO 00000
Frm 00133
Fmt 4703
Sfmt 4703
approved Evaluating the Overdose Data
to Action TA Hub (OMB Control No.
0920–1355, Exp. Date 11/30/2024) for
three years. CDC requests a three-year
OMB approval to support the evaluation
of technical assistance (TA) provided for
the Overdose Data to Action (OD2A) in
States (S) and OD2A: Limiting Overdose
through Collaborative Actions in
Localities (LOCAL) programs. OD2A–S
and OD2A: LOCAL are cooperative
agreements funded in 2023 to focus on
comprehensive and interdisciplinary
opioid overdose prevention efforts in 49
state health departments, 39 localities,
Puerto Rico, and Washington, DC. Each
program consists of two required
components—a surveillance component
and a prevention component. OD2A
recipients implement a combination of
activities across nine state strategies and
eight local strategies within these
components in order to gain access to
high quality, complete, and timelier
data on opioid prescribing and
overdoses and to use those data to
inform prevention and response efforts
in their jurisdictions.
In the previously approved iteration
of this data collection, the information
collected surrounding OD2A (version
1.0) recipient feedback on their
experiences receiving TA proved
invaluable in the process of improving
TA delivery and overall providing more
useful TA. The feedback provided in the
original data collection instruments was
also used to improve the TA Strategy of
the updated iterations of OD2A
(including OD2A–S and OD2A: LOCAL)
and their recipients. With the
information that was collected in the
previously approved ICR, CDC can more
effectively deliver TA to an almostdoubled recipient group across two
programs instead of one and ensure that
continuous improvement in TA is
occurring. Further information gathering
through the two new instruments
proposed in this ICR (the
Implementation Feedback Form and the
Focus Group script), will even more
acutely enhance TA perspectives and
needs to effectively and responsibly
utilize the DOP TA Center resource.
Training and technical assistance
(TA) is essential to building knowledge
and strengthening the capacity of
recipients to implement and evaluate
OD2A program strategies. CDC will
develop and deploy a TA hub (hereafter
referred to as the DOP TA Center) to
deliver comprehensive technical
assistance and training to support the
successful implementation and
evaluation of surveillance and
prevention activities. The DOP TA
Center is designed to enhance the
efficiency, coordination, and
E:\FR\FM\07MYN1.SGM
07MYN1
38151
Federal Register / Vol. 89, No. 89 / Tuesday, May 7, 2024 / Notices
effectiveness of TA efforts by
streamlining and centralizing the
provision of overdose surveillance and
prevention TA. TA to OD2A recipients
is divided into four different levels with
multiple modes of TA delivery and
involves a wide range of TA providers
appropriate resources to support their
needs.
CDC requests OMB approval for an
estimated 388 annual burden hours.
There is no cost to respondents other
than their time to participate.
including CDC staff, internal and
external subject matter experts (SMEs)
and program partners as well as Tanaq
and ICF staff. The four TA levels below
are used to direct the process for
engaging stakeholders to support
program recipients and triage
ESTIMATED ANNUALIZED BURDEN HOURS
Total burden
(in hours)
Form name
OD2A (OD2A in States and OD2A:
LOCAL) Recipients.
Individual TA Feedback Form ..........
618
2
5/60
103
Universal TA Feedback Form ..........
Implementation Feedback Survey ...
Annual Technical Assistance Survey
Email invitation for Annual ...............
Focus Group Session Script ............
Focus Groups Email invitation .........
617
18
162
900
100
600
2
1
1
........................
1
1
5/60
15/60
10/60
2/60
1
2/60
103
4.5
27
30
100
20
...........................................................
........................
........................
........................
388
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. 2024–09843 Filed 5–6–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–24–24FI; Docket No. CDC–2024–
0036]
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 and/or continuing
information collection, as required by
the Paperwork Reduction Act of 1995.
This notice invites comment on a
proposed information collection project
titled Comprehensive Evaluations of the
Division for Heart Disease and Stroke
Prevention Programs (WISEWOMAN,
National CVH Program, Innovative CVH
Program). The purpose of the data
collection is to evaluate the
SUMMARY:
khammond on DSKJM1Z7X2PROD with NOTICES
Average
burden per
response
(in hours)
Number of
responses per
respondent
Number of
respondents
Type of respondents
VerDate Sep<11>2014
15:55 May 06, 2024
Jkt 262001
implementation of evidence-based
strategies within these programs,
measure their impact on cardiovascular
disease (CVD) prevention and
management, and to identify strategies
that are most effective in reaching
populations disproportionately affected
by CVD.
DATES: CDC must receive written
comments on or before July 8, 2024.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2024–
0036 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: omb@
cdc.gov.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (PRA)
PO 00000
Frm 00134
Fmt 4703
Sfmt 4703
(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
E:\FR\FM\07MYN1.SGM
07MYN1
]]>Agencies
[Federal Register Volume 89, Number 89 (Tuesday, May 7, 2024)]
[Notices]
[Pages 38150-38151]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-09843]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-24-1355; Docket No. CDC-2024-0022]
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 continuing information
collection, as required by the Paperwork Reduction Act of 1995. This
notice invites comment on a proposed information collection project
titled Evaluation of the Division of Overdose Prevention Technical
Assistance Center. This data collection allows CDC to collect
information from partner organizations regarding feedback on their
experiences receiving technical assistance.
DATES: CDC must receive written comments on or before July 8, 2024.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2024-
0022 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
Evaluation of the Division of Overdose Prevention Technical
Assistance Center (OMB Control No., 0920-1355, Exp. 11/30/202)--
Revision--National Center for Injury Prevention and Control (NCIPC),
Centers for Disease Control and Prevention (CDC).
Background and Brief Description
The Centers for Disease Control and Prevention (CDC) is submitting
a Revision request for the currently approved Evaluating the Overdose
Data to Action TA Hub (OMB Control No. 0920-1355, Exp. Date 11/30/2024)
for three years. CDC requests a three-year OMB approval to support the
evaluation of technical assistance (TA) provided for the Overdose Data
to Action (OD2A) in States (S) and OD2A: Limiting Overdose through
Collaborative Actions in Localities (LOCAL) programs. OD2A-S and OD2A:
LOCAL are cooperative agreements funded in 2023 to focus on
comprehensive and interdisciplinary opioid overdose prevention efforts
in 49 state health departments, 39 localities, Puerto Rico, and
Washington, DC. Each program consists of two required components--a
surveillance component and a prevention component. OD2A recipients
implement a combination of activities across nine state strategies and
eight local strategies within these components in order to gain access
to high quality, complete, and timelier data on opioid prescribing and
overdoses and to use those data to inform prevention and response
efforts in their jurisdictions.
In the previously approved iteration of this data collection, the
information collected surrounding OD2A (version 1.0) recipient feedback
on their experiences receiving TA proved invaluable in the process of
improving TA delivery and overall providing more useful TA. The
feedback provided in the original data collection instruments was also
used to improve the TA Strategy of the updated iterations of OD2A
(including OD2A-S and OD2A: LOCAL) and their recipients. With the
information that was collected in the previously approved ICR, CDC can
more effectively deliver TA to an almost-doubled recipient group across
two programs instead of one and ensure that continuous improvement in
TA is occurring. Further information gathering through the two new
instruments proposed in this ICR (the Implementation Feedback Form and
the Focus Group script), will even more acutely enhance TA perspectives
and needs to effectively and responsibly utilize the DOP TA Center
resource.
Training and technical assistance (TA) is essential to building
knowledge and strengthening the capacity of recipients to implement and
evaluate OD2A program strategies. CDC will develop and deploy a TA hub
(hereafter referred to as the DOP TA Center) to deliver comprehensive
technical assistance and training to support the successful
implementation and evaluation of surveillance and prevention
activities. The DOP TA Center is designed to enhance the efficiency,
coordination, and
[[Page 38151]]
effectiveness of TA efforts by streamlining and centralizing the
provision of overdose surveillance and prevention TA. TA to OD2A
recipients is divided into four different levels with multiple modes of
TA delivery and involves a wide range of TA providers including CDC
staff, internal and external subject matter experts (SMEs) and program
partners as well as Tanaq and ICF staff. The four TA levels below are
used to direct the process for engaging stakeholders to support program
recipients and triage appropriate resources to support their needs.
CDC requests OMB approval for an estimated 388 annual burden hours.
There is no cost to respondents other than their time to participate.
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)
----------------------------------------------------------------------------------------------------------------
OD2A (OD2A in States and OD2A: Individual TA 618 2 5/60 103
LOCAL) Recipients. Feedback Form.
Universal TA 617 2 5/60 103
Feedback Form.
Implementation 18 1 15/60 4.5
Feedback Survey.
Annual Technical 162 1 10/60 27
Assistance
Survey.
Email invitation 900 .............. 2/60 30
for Annual.
Focus Group 100 1 1 100
Session Script.
Focus Groups 600 1 2/60 20
Email
invitation.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 388
----------------------------------------------------------------------------------------------------------------
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. 2024-09843 Filed 5-6-24; 8:45 am]
BILLING CODE 4163-18-P
