Proposed Data Collection Submitted for Public Comment and Recommendations, 47963-47965 [2024-12233]
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<![CDATA[
47963
Federal Register / Vol. 89, No. 108 / Tuesday, June 4, 2024 / Notices
collection forms. In this Revision, CDC
requests OMB approval for an estimated
annual burden of 6,455,846 hours.
There is no cost to respondents other
than their time to participate.
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondent
Form No.
Form
Microbiologist ...........
57.102
Microbiologist ...........
57.103
Microbiologist ...........
57.140
57.144
Microbiologist ...........
57.145
Microbiologist
Microbiologist
Microbiologist
Microbiologist
...........
...........
...........
...........
57.155
57.159
57.160
57.218
Microbiologist ...........
57.219
Microbiologist ...........
57.220
Microbiologist ...........
57.220
Microbiologist ...........
57.221
Microbiologist ...........
57.221
Microbiologist ...........
57.221
Microbiologist ...........
57.221
Microbiologist ...........
57.509
Microbiologist ...........
57.510
COVID–19 Hospital Data Form (excluding Psychiatric and Rehabilitation Facilities).
COVID–19 Hospital Data Form (Psychiatric and Rehabilitation Facilities).
National Healthcare Safety Network (NHSN) Registration Form .....
COVID–19 and Respiratory Pathogens Module Long Term Care
Facility: Resident Impact and Facility Capacity Pathway.
COVID–19 Module, Long Term Care Facility: Staff and Personnel
Impact form.
Point of Care Testing Results ..........................................................
VA Resident COVID–19 Event Form-LTCF .....................................
VA Staff and Personnel COVID–19 Event Form-LTCF ...................
Weekly Respiratory Pathogen and Vaccination Summary for Residents of Long-Term Care Facilities (CSV).
Healthcare Personnel COVID–19 Vaccination Cumulative Summary (CSV).
Weekly Person Level Respiratory Pathogen and Vaccination for
Residents of Long-Term Care Facilities-Long-term Care Facility
Component (Manual Entry).
Weekly Person Level Respiratory Pathogen and Vaccination for
Residents of Long-Term Care Facilities-Long-term Care Facility
Component (CSV Entry).
Healthcare Personnel COVID–19 Person Level Vaccination-LongTerm Care Component (Manual).
Healthcare Personnel COVID–19 Person Level Vaccination-LongTerm Care Component (CSV).
Healthcare Personnel COVID–19 Person Level VaccinationHealthcare Personnel Safety Component (Manual).
Healthcare Personnel COVID–19 Person Level VaccinationHealthcare Personnel Safety Component (CSV).
Weekly Patient COVID–19 Vaccination Cumulative Summary for
Dialysis Facilities.
COVID–19 Module Dialysis Outpatient Facility ................................
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. 2024–12238 Filed 6–3–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–24–24FZ; Docket No. CDC–2024–
0048]
ddrumheller on DSK120RN23PROD with NOTICES1
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
SUMMARY:
VerDate Sep<11>2014
17:15 Jun 03, 2024
Jkt 262001
Number of
responses per
respondent
5,200
365
90/60
2,847,000
870
365
90/60
476,325
11,500
16,500
1
52
5/60
25/60
958
357,500
11,621
52
5/60
50,358
6,270
195
176
16,500
200
25
25
52
10/60
35/60
30/60
25/60
209,000
2,844
2,200
357,500
32,900
76
45/60
1,875,300
1,600
52
60/60
83,200
1,600
52
40/60
55,467
73
76
60/60
5,548
73
76
40/60
3,699
73
76
60/60
5,548
73
76
40/60
3,699
7,700
12
75/60
115,500
150
56
30/60
4,200
....................
........................
....................
6,455,846
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 Annual Progress
Reports for Injury Control Research
Centers (ICRC). ICRCs focus on research,
training, and outreach for issues of local
and national importance, including the
prevention of adverse childhood
experiences, child abuse and neglect,
drowning, drug overdose, intimate
partner violence, older adult falls,
sexual violence, suicide, and traumatic
brain injuries, as well as the promotion
of transportation safety.
CDC must receive written
comments on or before August 5, 2024.
DATES:
You may submit comments,
identified by Docket No. CDC–2024–
0048 by either of the following methods:
• Federal eRulemaking Portal:
www.regulations.gov. Follow the
instructions for submitting comments.
ADDRESSES:
PO 00000
Frm 00072
Fmt 4703
Sfmt 4703
Average
burden per
response
(in hours)
Number of
respondents
Total
burden
(in hours)
• 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
E:\FR\FM\04JNN1.SGM
04JNN1
47964
Federal Register / Vol. 89, No. 108 / Tuesday, June 4, 2024 / Notices
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
Annual Progress Reports for Injury
Control Research Centers (ICRC)—
New—National Center for Injury
Prevention and Control (NCIPC),
Centers for Disease Control and
Prevention (CDC).
prevention and control. ICRC grants are
typically funded in five-year funding
cycles. The Centers for Disease Control
and Prevention (CDC) requests OMB
approval to electronically collect annual
progress report (APR) information and
Success Stories from the 11 currently
funded ICRCs. Grantees will report
progress and activity information to
CDC on an annual schedule using a
web-based CAMP. The information that
will be collected will provide crucial
data for program performance
monitoring and will improve CDC’s
ability 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. The
information that will be collected will
also strengthen CDC’s ability to monitor
grantee progress towards stated grant
research, training, and outreach
objectives, provide data-driven
technical assistance, and disseminate
Success Stories about what’s working to
reduce unintentional and intentional
injuries. This data collection will
improve and innovate through
evaluation, research, and quality
improvement; investigate, diagnose, and
address health hazards and root causes;
communicate effectively to inform and
educate; strengthen, support, and
mobilize communities and partnerships;
and create, champion, and implement
policies, plans. CDC ICRC grantees
perform all of these activities, and the
systematic collection of data, annually,
is the best way for CDC to understand
this work. This APR information
collection will enable grantees to submit
accurate, reliable, and timely activity
and performance data to the CDC.
Background and Brief Description
In 1987, the Centers for Disease
Control and Prevention (CDC) and the
National Center for Injury Prevention
and Control (NCIPC) began funding
Injury Control Research Centers (ICRCs)
at academic research institutions
throughout the United States. ICRCs
focus on three core functions—research,
training, and outreach—for issues of
local and national importance,
including the prevention of adverse
childhood experiences; child abuse and
neglect; drowning; drug overdose;
intimate partner violence; older adult
falls; sexual violence; suicide; and
traumatic brain injuries, and the
promotion of transportation safety.
ICRCs foster multidisciplinary strategies
for addressing these complex problems
and disseminating research findings. In
addition to conducting cutting-edge,
multidisciplinary research, ICRCs train
and develop the current and next
generation of researchers and public
health professionals to help ensure that
there is an adequate supply of qualified
practitioners and researchers for
advancing prevention research,
addressing new problems, and reaching
new populations across the nation.
Finally, ICRCs work with States and
communities to translate research
findings into action. ICRCs provide
partner organizations with technical
assistance on programs, public health
infrastructure, and the integration of
resources at the local, State, and
national levels. Areas of emphasis
within each ICRC are determined by the
expertise of the faculty and the public
health needs and opportunities
identified through the ICRC’s outreach
activities. This collaborative approach is
a vital component in the success of
efforts to make an impact on
population-level reduction in injuryrelated harm.
ICRCs form a national network of
expertise and innovation in injury
CDC requests OMB approval for an
estimated 183 annual burden hours.
There is no cost to participants other
than their time.
ESTIMATED ANNUALIZED BURDEN HOURS
ddrumheller on DSK120RN23PROD with NOTICES1
Type of respondents
Injury Research Center (ICRC) Grantees.
Total ...............................................
VerDate Sep<11>2014
17:15 Jun 03, 2024
Number of
respondents
Form name
Jkt 262001
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total
burden
(in hours)
Injury Control Research Indicators
Data Collection.
ICRC Publication Table ........................
Success Stories Template ...................
11
1
8
88
11
11
1
1
8
1
88
7
...............................................................
........................
........................
....................
183
PO 00000
Frm 00073
Fmt 4703
Sfmt 4703
E:\FR\FM\04JNN1.SGM
04JNN1
Federal Register / Vol. 89, No. 108 / Tuesday, June 4, 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. 2024–12233 Filed 6–3–24; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–24–0572; Docket No. CDC–2024–
0044]
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 Health Message
Testing System (HMTS). The HMTS is
a Generic information collection that
enables programs across CDC to test
proposed health messages on a target
audience before these messages are
disseminated to the public.
DATES: CDC must receive written
comments on or before August 5, 2024.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2024–
0044 by any 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
ddrumheller on DSK120RN23PROD with NOTICES1
SUMMARY:
VerDate Sep<11>2014
17:15 Jun 03, 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
Health Message Testing System
(HMTS) (OMB Control No. 0920–0572,
Exp. 10/31/2024)—Extension—Office of
Communication (OC), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
Before CDC disseminates a health
message to the public, the message
always undergoes scientific review.
However, even though the message is
based on sound scientific content, there
is no guarantee that the public will
PO 00000
Frm 00074
Fmt 4703
Sfmt 4703
47965
understand a health message or that the
message will move people to take
recommended action. Communication
theorists and researchers agree that for
health messages to be as clear and
influential as possible, target audience
members or representatives must be
involved in developing the messages
and provisional versions of the
messages must be tested with members
of the target audience. Increasingly there
are circumstances when CDC must
move swiftly to protect life, prevent
disease, or calm public anxiety. Health
message testing is even more important
in these instances, because of the
critical nature of the information need.
In the interest of timely health
message dissemination, many programs
forgo the important step of testing
messages on dimensions such as clarity,
salience, appeal, and persuasiveness
(i.e., the ability to influence behavioral
intention). Skipping this step avoids the
delay involved in the standard OMB
review process, but at a high potential
cost. Untested messages can waste
communication resources and
opportunities because the messages can
be perceived as unclear or irrelevant.
Untested messages can also have
unintended consequences, such as
jeopardizing the credibility of Federal
health officials.
The Health Message Testing System
(HMTS) is a Generic information
collection, that enables programs across
CDC to collect the information they
require in a timely manner to:
• Ensure quality and prevent waste in
the dissemination of health information
by CDC to the public.
• Refine message concepts and to test
draft materials for clarity, salience,
appeal, and persuasiveness to target
audiences.
• Guide the action of health
communication officials who are
responding to health emergencies,
Congressionally-mandated campaigns
with short timeframes, media-generated
public concern, time-limited
communication opportunities, trends,
and the need to refresh materials or
dissemination strategies in an ongoing
campaign.
Each testing instrument will be based
on specific health issues or topics.
Although it is not possible to develop
one instrument for use in all instances,
the same kinds of questions are asked in
most message testing. This package
includes generic questions and formats
that can be used to develop health
message testing data collection
instruments. These include a list of
screening questions, comprised of
demographic and introductory
questions, along with other questions
E:\FR\FM\04JNN1.SGM
04JNN1
]]>Agencies
[Federal Register Volume 89, Number 108 (Tuesday, June 4, 2024)]
[Notices]
[Pages 47963-47965]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-12233]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-24-24FZ; Docket No. CDC-2024-0048]
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 Annual Progress Reports for Injury Control Research Centers
(ICRC). ICRCs focus on research, training, and outreach for issues of
local and national importance, including the prevention of adverse
childhood experiences, child abuse and neglect, drowning, drug
overdose, intimate partner violence, older adult falls, sexual
violence, suicide, and traumatic brain injuries, as well as the
promotion of transportation safety.
DATES: CDC must receive written comments on or before August 5, 2024.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2024-
0048 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
[[Page 47964]]
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
Annual Progress Reports for Injury Control Research Centers
(ICRC)--New--National Center for Injury Prevention and Control (NCIPC),
Centers for Disease Control and Prevention (CDC).
Background and Brief Description
In 1987, the Centers for Disease Control and Prevention (CDC) and
the National Center for Injury Prevention and Control (NCIPC) began
funding Injury Control Research Centers (ICRCs) at academic research
institutions throughout the United States. ICRCs focus on three core
functions--research, training, and outreach--for issues of local and
national importance, including the prevention of adverse childhood
experiences; child abuse and neglect; drowning; drug overdose; intimate
partner violence; older adult falls; sexual violence; suicide; and
traumatic brain injuries, and the promotion of transportation safety.
ICRCs foster multidisciplinary strategies for addressing these complex
problems and disseminating research findings. In addition to conducting
cutting-edge, multidisciplinary research, ICRCs train and develop the
current and next generation of researchers and public health
professionals to help ensure that there is an adequate supply of
qualified practitioners and researchers for advancing prevention
research, addressing new problems, and reaching new populations across
the nation. Finally, ICRCs work with States and communities to
translate research findings into action. ICRCs provide partner
organizations with technical assistance on programs, public health
infrastructure, and the integration of resources at the local, State,
and national levels. Areas of emphasis within each ICRC are determined
by the expertise of the faculty and the public health needs and
opportunities identified through the ICRC's outreach activities. This
collaborative approach is a vital component in the success of efforts
to make an impact on population-level reduction in injury-related harm.
ICRCs form a national network of expertise and innovation in injury
prevention and control. ICRC grants are typically funded in five-year
funding cycles. The Centers for Disease Control and Prevention (CDC)
requests OMB approval to electronically collect annual progress report
(APR) information and Success Stories from the 11 currently funded
ICRCs. Grantees will report progress and activity information to CDC on
an annual schedule using a web-based CAMP. The information that will be
collected will provide crucial data for program performance monitoring
and will improve CDC's ability 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. The information that will be collected will also strengthen
CDC's ability to monitor grantee progress towards stated grant
research, training, and outreach objectives, provide data-driven
technical assistance, and disseminate Success Stories about what's
working to reduce unintentional and intentional injuries. This data
collection will improve and innovate through evaluation, research, and
quality improvement; investigate, diagnose, and address health hazards
and root causes; communicate effectively to inform and educate;
strengthen, support, and mobilize communities and partnerships; and
create, champion, and implement policies, plans. CDC ICRC grantees
perform all of these activities, and the systematic collection of data,
annually, is the best way for CDC to understand this work. This APR
information collection will enable grantees to submit accurate,
reliable, and timely activity and performance data to the CDC.
CDC requests OMB approval for an estimated 183 annual burden hours.
There is no cost to participants other than their time.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total
Type of respondents Form name respondents responses per response burden (in
respondent (in hours) hours)
----------------------------------------------------------------------------------------------------------------
Injury Research Center (ICRC) Injury Control 11 1 8 88
Grantees. Research
Indicators Data
Collection.
ICRC Publication 11 1 8 88
Table.
Success Stories 11 1 1 7
Template.
---------------------------------------------------------
Total........................ ................... .............. .............. ........... 183
----------------------------------------------------------------------------------------------------------------
[[Page 47965]]
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. 2024-12233 Filed 6-3-24; 8:45 am]
BILLING CODE 4163-18-P
