Proposed Data Collection Submitted for Public Comment and Recommendations, 3992-3994 [2023-01162]
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Federal Register / Vol. 88, No. 14 / Monday, January 23, 2023 / Notices
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
Information Collections to Advance
State, Tribal, Local, and Territorial
(STLT) Governmental Agency and
System Performance, Capacity, and
Program Delivery—Extension—Center
for State, Tribal, Local and Territorial
office or individual) acting for a
principal or submitted by another to
represent or act on their behalf. The
STLT agency is represented by a STLT
entity or delegate with a task to protect
and/or improve the public’s health.
Information will be used to: (1) assess
situational awareness of current public
health emergencies; (2) make decisions
that affect planning, response and
recovery activities of subsequent
emergencies; (3) fill CDC and HHS gaps
in knowledge of programs and/or STLT
governments that will strengthen
surveillance, epidemiology, and
laboratory science; and (4) improve
CDC’s support and technical assistance
to states and communities. CDC and
HHS will conduct brief data collections,
across a range of public health topics
related to essential public health
services.
CDC estimates up to 30 data
collections with STLT governmental
staff or delegates, and 10 data
collections with local/county/city
governmental staff or delegates will be
conducted on an annual basis.
Approximately 95% of these data
collections will be web-based and 5%
will be conducted via telephone, inperson, or focus groups.
CDC requests OMB approval for an
estimated 54,000 annual burden hours.
There are no costs to respondents other
than their time to participate.
Support (CSTLTS), Centers for Disease
Control and Prevention (CDC).
Background and Brief Description
The mission of the Department of
Health and Human Services (HHS) is to
enhance the health and well-being of all
Americans. As part of HHS, CDC
conducts critical science and provides
health information to people and
communities to save lives and protect
people from health threats. To this end,
CDC and HHS seek to accomplish their
mission by collaborating with partners
throughout the nation and the world to
monitor health, detect and investigate
health problems, conduct research to
enhance prevention, develop and
advocate sound public health policies,
implement prevention strategies,
promote healthy behaviors, foster safe
and healthful environments, and
provide leadership and training.
CDC is requesting a three-year
approval to extend a Generic clearance
to collect information related to
domestic public health issues and
services that affect and/or involve State,
Tribal, Local, and Territorial (STLT)
government entities. The respondent
universe is comprised of STLT
governmental staff or delegates acting
on behalf of a STLT agency involved in
the provision of essential public health
services in the United States. Delegate is
defined as a governmental or nongovernmental agent (agency, function,
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
Number of
respondents
Form name
State, Territorial, or Tribal government staff or delegate.
Local/County/City government staff
or delegate.
Total ...........................................
Web, telephone, in-person, focus
group.
Web, telephone, in-person, focus
group.
...........................................................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2023–01161 Filed 1–20–23; 8:45 am]
1
24,000
3,000
10
1
30,000
........................
........................
........................
54,000
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
khammond on DSKJM1Z7X2PROD with NOTICES
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:
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Total burden
(in hrs.)
30
[60Day–23–0910; Docket No. CDC–2023–
0004]
16:44 Jan 20, 2023
Average
burden per
respondent
(in hrs.)
800
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Number of
responses per
respondent
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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 Message Testing for Tobacco
Communication Activities (MTTCA).
The primary purpose and use of
information collected under MTTCA is
to inform the development and
SUMMARY:
E:\FR\FM\23JAN1.SGM
23JAN1
khammond on DSKJM1Z7X2PROD with NOTICES
Federal Register / Vol. 88, No. 14 / Monday, January 23, 2023 / Notices
pretesting of materials for the CDC’s
ongoing National Tobacco Education
Campaign (NTEC), and other health
messages that are not specifically
associated with the NTEC (e.g., Surgeon
General’s Reports).
DATES: CDC must receive written
comments on or before March 24, 2023.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2023–
0004 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
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
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
VerDate Sep<11>2014
16:44 Jan 20, 2023
Jkt 259001
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
Message Testing for Tobacco
Communication Activities (MTTCA)
(OMB Control No. 0920–0910, Exp. 01/
31/2024)—Revision—National Center
for Chronic Disease Prevention and
Health Promotion (NCCDPH), Centers
for Disease Control and Prevention
(CDC).
Background and Brief Description
CDC has employed the Message
Testing for Tobacco Communication
Activities (MTTCA, OMB Control No.
0920–0910) clearance since 2012. The
MTTCA clearance collects information
about attitudes and perceptions among
adults who smoke and adults who don’t
smoke, and is designed to pretest draft
messages and materials for clarity,
salience, appeal, and persuasiveness.
The MTTCA clearance has been used to
obtain OMB approval for a variety of
message testing activities, with
particular emphasis on communications
supporting CDC’s National Tobacco
Education Campaign (NTEC) called the
Tips From Former Smokers® campaign.
This national campaign is designed to
increase public awareness of the health
consequences of tobacco use and
exposure to secondhand smoke. The
MTTCA clearance has also supported
formative research relating to the
development of health messages for a
campaign to encourage educators to
speak with middle and high school
students about the risks of e-cigarette
use and empower them to avoid or quit
e-cigarettes.
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Fmt 4703
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3993
Information collection modes under
the MTTCA clearance that are
supported include in-person and online
in-depth interviews; in-person and
online focus groups; and online surveys.
Each project approved under the
MTTCA framework is outlined in a
project specific Generic Information
Collection Request (GenIC) that
describes its purpose and methodology.
Messages developed from MTTCA data
collection have been disseminated via
multiple media channels including
television, radio, print, out-of-home,
and digital formats.
CDC requests OMB approval for a
Revision to the MTTCA clearance, for
three years. Requested changes are to
increase the number of respondents and
burden hours. These adjustments will
support data collections among people
who smoke and people who do not
smoke, including, but not limited to,
people who smoke and are members of
populations that are disproportionately
affected by commercial tobacco (e.g.,
people from racial and ethnic minority
groups, people who are LGBTQ+,
people of lower socioeconomic status,
etc.), adult influencers of middle and
high school students (e.g., educators,
parents and health care providers), and
youth aged 13–17 years. No
modification is requested for
information collection activities,
methodology, or populations of interest
from the existing Generic Clearance.
This Revision and requested changes
are needed to support CDC’s planned
information collections and to
accommodate additional needs that CDC
may identify during the next three
years. For example, the MTTCA Generic
Clearance may be used to facilitate the
development of tobacco-related health
communications of interest for CDC’s
collaborative efforts with other federal
partners including, but not limited to,
the Food and Drug Administration’s
(FDA) Center for Tobacco Products. The
MTTCA clearance should not replace
the need for additional Generic
Clearance mechanisms of HHS and
other federal partners that may need to
test tobacco messages related to their
campaigns and initiatives.
CDC requests OMB approval for an
estimated 20,039 annualized burden
hours. Participation is voluntary and
there are no costs to respondents other
than their time.
E:\FR\FM\23JAN1.SGM
23JAN1
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Federal Register / Vol. 88, No. 14 / Monday, January 23, 2023 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
General Public
lations.
General Public
lations.
General Public
lations.
General Public
lations.
General Public
lations.
Total burden
(in hours)
and Special Popu-
Screening .........................................
74,386
1
2/60
2,480
and Special Popu-
25
1
1
25
and Special Popu-
In-Depth Interviews (Online, In Person).
Focus Groups (Online, In Person) ...
628
1
1.5
942
and Special Popu-
Surveys (Online, Short) ....................
71,000
1
15,453
and Special Popu-
Surveys (Online, Medium) ...............
2,733
1
20/60
13/60
25/60
...........................................................
........................
........................
........................
20,039
Total ...........................................
Jeffrey M. Zirger,
The Office of Child Support
Enforcement (OCSE), Administration for
Children and Families (ACF), is
requesting the federal Office of
Management and Budget (OMB) to
extend approval of the Income
Withholding for Support Order (IWO),
with minor changes, for an additional 3
years. The current OMB approval
expires September 30, 2023.
SUMMARY:
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2023–01162 Filed 1–20–23; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Proposed Information Collection
Activity; Income Withholding for
Support Order (OMB No.: 0970–0154)
Office of Child Support
Enforcement, Administration for
Children and Families, Department of
Health and Human Services.
AGENCY:
Request for public comments.
Comments due within 60 days of
publication. In compliance with the
requirements of the Paperwork
Reduction Act of 1995, ACF is soliciting
public comment on the specific aspects
of the information collection described
above.
DATES:
Administration for Children and
Families
ACTION:
Average
burden per
response
(in hours)
Number of
responses per
respondent
Number of
respondents
Form name
You can obtain copies of the
proposed collection of information and
submit comments by emailing
infocollection@acf.hhs.gov. All requests
should be identified by the title of the
information collection.
ADDRESSES:
1,139
SUPPLEMENTARY INFORMATION:
Description: The IWO is the required,
standard form used to order, and notify,
employers and income providers to
withhold child support payments from
an obligor’s income. It is also used to
notify employers and other income
providers where to remit the payments,
as well as other information needed to
correctly withhold payments so that
children and families receive the
support to which they are entitled.
The IWO form instructions underwent
minor edits to clarify the language and
improve the respondent’s ability to
properly complete the IWO Form. The
burden estimates changed to reflect
current estimates for the annual number
of respondents and responses.
Respondents: Courts, private
attorneys, custodial parties or their
representatives, employers, and other
entities that provide income to
noncustodial parents.
ANNUAL BURDEN ESTIMATES
khammond on DSKJM1Z7X2PROD with NOTICES
Income withholding order/notice (Courts, private attorneys, custodial parties
or their representatives).
Income withholding orders/termination of employment/income status (Employers and other income providers).
Electronic income withholding orders/termination of employment/income status (Employers and other income providers).
VerDate Sep<11>2014
16:44 Jan 20, 2023
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PO 00000
Frm 00029
Total annual
number of
responses per
respondent
Average
burden hours
per response
4,694,517
1
5 minutes ....
391,210
1,277,952
8.01
2 minutes ....
341,213
33,746
67.70
30 seconds ..
19,038
Total annual
number of
respondents
Information collection instrument
Fmt 4703
Sfmt 4703
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23JAN1
Total annual
burden hours
]]>Agencies
[Federal Register Volume 88, Number 14 (Monday, January 23, 2023)]
[Notices]
[Pages 3992-3994]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-01162]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60Day-23-0910; Docket No. CDC-2023-0004]
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 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 Message Testing for Tobacco
Communication Activities (MTTCA). The primary purpose and use of
information collected under MTTCA is to inform the development and
[[Page 3993]]
pretesting of materials for the CDC's ongoing National Tobacco
Education Campaign (NTEC), and other health messages that are not
specifically associated with the NTEC (e.g., Surgeon General's
Reports).
DATES: CDC must receive written comments on or before March 24, 2023.
ADDRESSES: You may submit comments, identified by Docket No. CDC-2023-
0004 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 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: [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
Message Testing for Tobacco Communication Activities (MTTCA) (OMB
Control No. 0920-0910, Exp. 01/31/2024)--Revision--National Center for
Chronic Disease Prevention and Health Promotion (NCCDPH), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
CDC has employed the Message Testing for Tobacco Communication
Activities (MTTCA, OMB Control No. 0920-0910) clearance since 2012. The
MTTCA clearance collects information about attitudes and perceptions
among adults who smoke and adults who don't smoke, and is designed to
pretest draft messages and materials for clarity, salience, appeal, and
persuasiveness. The MTTCA clearance has been used to obtain OMB
approval for a variety of message testing activities, with particular
emphasis on communications supporting CDC's National Tobacco Education
Campaign (NTEC) called the Tips From Former Smokers[supreg] campaign.
This national campaign is designed to increase public awareness of the
health consequences of tobacco use and exposure to secondhand smoke.
The MTTCA clearance has also supported formative research relating to
the development of health messages for a campaign to encourage
educators to speak with middle and high school students about the risks
of e-cigarette use and empower them to avoid or quit e-cigarettes.
Information collection modes under the MTTCA clearance that are
supported include in-person and online in-depth interviews; in-person
and online focus groups; and online surveys. Each project approved
under the MTTCA framework is outlined in a project specific Generic
Information Collection Request (GenIC) that describes its purpose and
methodology. Messages developed from MTTCA data collection have been
disseminated via multiple media channels including television, radio,
print, out-of-home, and digital formats.
CDC requests OMB approval for a Revision to the MTTCA clearance,
for three years. Requested changes are to increase the number of
respondents and burden hours. These adjustments will support data
collections among people who smoke and people who do not smoke,
including, but not limited to, people who smoke and are members of
populations that are disproportionately affected by commercial tobacco
(e.g., people from racial and ethnic minority groups, people who are
LGBTQ+, people of lower socioeconomic status, etc.), adult influencers
of middle and high school students (e.g., educators, parents and health
care providers), and youth aged 13-17 years. No modification is
requested for information collection activities, methodology, or
populations of interest from the existing Generic Clearance.
This Revision and requested changes are needed to support CDC's
planned information collections and to accommodate additional needs
that CDC may identify during the next three years. For example, the
MTTCA Generic Clearance may be used to facilitate the development of
tobacco-related health communications of interest for CDC's
collaborative efforts with other federal partners including, but not
limited to, the Food and Drug Administration's (FDA) Center for Tobacco
Products. The MTTCA clearance should not replace the need for
additional Generic Clearance mechanisms of HHS and other federal
partners that may need to test tobacco messages related to their
campaigns and initiatives.
CDC requests OMB approval for an estimated 20,039 annualized burden
hours. Participation is voluntary and there are no costs to respondents
other than their time.
[[Page 3994]]
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)
----------------------------------------------------------------------------------------------------------------
General Public and Special Screening....... 74,386 1 2/60 2,480
Populations.
General Public and Special In-Depth 25 1 1 25
Populations. Interviews
(Online, In
Person).
General Public and Special Focus Groups 628 1 1.5 942
Populations. (Online, In
Person).
General Public and Special Surveys (Online, 71,000 1 20/60 15,453
Populations. Short). 13/60
General Public and Special Surveys (Online, 2,733 1 25/60 1,139
Populations. Medium).
---------------------------------------------------------------
Total..................... ................ .............. .............. .............. 20,039
----------------------------------------------------------------------------------------------------------------
Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific
Integrity, Office of Science, Centers for Disease Control and
Prevention.
[FR Doc. 2023-01162 Filed 1-20-23; 8:45 am]
BILLING CODE 4163-18-P
