Proposed Data Collection Submitted for Public Comment and Recommendations, 30366-30367 [2024-08594]
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30366
Federal Register / Vol. 89, No. 79 / Tuesday, April 23, 2024 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
REACH
REACH
REACH
REACH
REACH
REACH
REACH
Average
burden per
response
(in hrs.)
Total burden
(in hrs.)
Recipient Data Manager .....
Recipient Data Manager .....
Clients ..................................
Recipient/Clinic Staff ...........
Recipient/Clinic Staff ...........
Clients ..................................
Recipient Data Manager .....
Electronic Health Record Data Form
Client Info Form ...............................
Client Info Form ...............................
Client Info Form ...............................
Provider Info Form ...........................
Client Program Evaluation Survey ...
Client Program Evaluation Survey ...
5
5
500
5
5
100
5
2
2
1
100
10
1
2
8
2
6/60
6/60
6/60
42/60
2
80
20
50
50
5
70
20
Total ...........................................
..........................................................
........................
........................
........................
295
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. 2024–08595 Filed 4–22–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–2024–24EO; Docket No. CDC–2024–
0027]
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 Evaluation of
HIV Self-Testing and Clinical Testing
Guidelines Implementation. This project
is designed to collect data from HIV
healthcare providers, working in various
settings, on the awareness and uptake of
HIV-related guidelines.
DATES: CDC must receive written
comments on or before June 24, 2024.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2024–
0027 by either of the following methods:
• Federal eRulemaking Portal:
www.regulations.gov. Follow the
instructions for submitting comments.
SUMMARY:
ddrumheller on DSK120RN23PROD with NOTICES1
Number of
responses per
respondent
Number of
respondents
Form name
VerDate Sep<11>2014
17:48 Apr 22, 2024
Jkt 262001
• 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)
(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
PO 00000
Frm 00047
Fmt 4703
Sfmt 4703
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 HIV Self-Testing and
Clinical Testing Guidelines
Implementation—New—National
Centers for HIV, Viral Hepatitis, STD,
and TB Prevention (NCHHSTP), Centers
for Disease Control and Prevention
(CDC).
Background and Brief Description
It takes several years and a significant
number of staff and resources to develop
and disseminate guidelines. The
Division of HIV Prevention (DHP) has
been a leader in informing providers
and program staff when it comes to HIV
prevention through respective
guidelines. Yet, DHP’s understanding of
the awareness and use of HIV-related
guidelines has been limited. There have
been few efforts and resources dedicated
to assessing and evaluating guideline
implementation. With DHP’s impending
completion and publication of the HIV
self-testing and updated HIV testing
guidelines in 2024, this project proposes
a mixed methods approach to evaluate
the awareness and uptake of these
guidelines by providers using
quantitative and qualitative methods.
These providers include those who
E:\FR\FM\23APN1.SGM
23APN1
30367
Federal Register / Vol. 89, No. 79 / Tuesday, April 23, 2024 / Notices
work in health departments, community
health centers, clinics, or communitybased organizations.
The purpose of this data collection is
to: (a) assess the awareness and use of
the HIV self-testing and HIV testing
guidelines by healthcare providers
working in different health settings; (b)
understand the barriers and facilitators
to uptake of guidelines; and (c) inform
CDC efforts to support guideline
implementation through training,
promotion, or technical assistance. The
new HIV self-testing guideline and
updated HIV testing guideline are yet to
be published. This project is the first
attempt to evaluate these guidelines and
interview or survey. These data may
inform prevention program
development and monitoring, resource
allocation, and technical assistance
needs at both the local and national
levels. CDC estimates that this data
collection will involve, 1100 surveys
and 120 interviews in specific settings
(community health centers, health
departments, private clinics, public
clinics, hospitals, and community-based
organizations) over the course of three
years. CDC requests OMB approval for
an estimated 610 annual burden hours.
Participation of respondents is
voluntary and there is no cost to the
respondents other than their time.
as such, no other Federal agency
systematically collects this type of
information from healthcare providers
that supply HIV testing services. This
data collection will allow DHP to
understand how guidelines are being
implemented in the early days of release
and inform efforts including resource
allocation for guideline development,
translation, and implementation efforts.
CDC requests approval for a three-year
information collection. Data are
collected through surveys and virtual or
phone interviews conducted with
healthcare providers. There is no
monetary compensation or incentives
provided for participation in the
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
(in hours)
Form name
Eligible Providers ..............................
Eligible Providers ..............................
Survey ..............................................
Interview Questionnaire ...................
1,100
120
1
1
30/60
30/60
550
60
Total ...........................................
..........................................................
........................
........................
........................
610
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. 2024–08594 Filed 4–22–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–24–0666; Docket No. CDC–2024–
0030]
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 National Healthcare Safety
SUMMARY:
ddrumheller on DSK120RN23PROD with NOTICES1
Number of
respondents
Type of respondents
VerDate Sep<11>2014
17:48 Apr 22, 2024
Jkt 262001
Network (NHSN). NHSN provides
facilities, States, regions, and the nation
with data necessary to identify problem
areas, measure the progress of
prevention efforts, and ultimately
eliminate healthcare-associated
infections (HAIs) nationwide.
DATES: CDC must receive written
comments on or before June 24, 2024.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2024–
0030 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;
PO 00000
Frm 00048
Fmt 4703
Sfmt 4703
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;
E:\FR\FM\23APN1.SGM
23APN1
]]>Agencies
[Federal Register Volume 89, Number 79 (Tuesday, April 23, 2024)]
[Notices]
[Pages 30366-30367]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-08594]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-2024-24EO; Docket No. CDC-2024-0027]
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 Evaluation of HIV Self-Testing and Clinical Testing Guidelines
Implementation. This project is designed to collect data from HIV
healthcare providers, working in various settings, on the awareness and
uptake of HIV-related guidelines.
DATES: CDC must receive written comments on or before June 24, 2024.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2024-
0027 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 HIV Self-Testing and Clinical Testing Guidelines
Implementation--New--National Centers for HIV, Viral Hepatitis, STD,
and TB Prevention (NCHHSTP), Centers for Disease Control and Prevention
(CDC).
Background and Brief Description
It takes several years and a significant number of staff and
resources to develop and disseminate guidelines. The Division of HIV
Prevention (DHP) has been a leader in informing providers and program
staff when it comes to HIV prevention through respective guidelines.
Yet, DHP's understanding of the awareness and use of HIV-related
guidelines has been limited. There have been few efforts and resources
dedicated to assessing and evaluating guideline implementation. With
DHP's impending completion and publication of the HIV self-testing and
updated HIV testing guidelines in 2024, this project proposes a mixed
methods approach to evaluate the awareness and uptake of these
guidelines by providers using quantitative and qualitative methods.
These providers include those who
[[Page 30367]]
work in health departments, community health centers, clinics, or
community-based organizations.
The purpose of this data collection is to: (a) assess the awareness
and use of the HIV self-testing and HIV testing guidelines by
healthcare providers working in different health settings; (b)
understand the barriers and facilitators to uptake of guidelines; and
(c) inform CDC efforts to support guideline implementation through
training, promotion, or technical assistance. The new HIV self-testing
guideline and updated HIV testing guideline are yet to be published.
This project is the first attempt to evaluate these guidelines and as
such, no other Federal agency systematically collects this type of
information from healthcare providers that supply HIV testing services.
This data collection will allow DHP to understand how guidelines are
being implemented in the early days of release and inform efforts
including resource allocation for guideline development, translation,
and implementation efforts.
CDC requests approval for a three-year information collection. Data
are collected through surveys and virtual or phone interviews conducted
with healthcare providers. There is no monetary compensation or
incentives provided for participation in the interview or survey. These
data may inform prevention program development and monitoring, resource
allocation, and technical assistance needs at both the local and
national levels. CDC estimates that this data collection will involve,
1100 surveys and 120 interviews in specific settings (community health
centers, health departments, private clinics, public clinics,
hospitals, and community-based organizations) over the course of three
years. CDC requests OMB approval for an estimated 610 annual burden
hours. Participation of respondents is voluntary and there is no cost
to the respondents other than their time.
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)
----------------------------------------------------------------------------------------------------------------
Eligible Providers............ Survey.......... 1,100 1 30/60 550
Eligible Providers............ Interview 120 1 30/60 60
Questionnaire.
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 610
----------------------------------------------------------------------------------------------------------------
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. 2024-08594 Filed 4-22-24; 8:45 am]
BILLING CODE 4163-18-P
