60 Day FRN

Attachment B-1. 60-day Federal Register Notice, Docket No. CDC_2022-0071.pdf

Extended Evaluation of the National Tobacco Prevention and Control Public Education Campaign

60 Day FRN

OMB: 0920-1083

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Federal Register / Vol. 87, No. 106 / Thursday, June 2, 2022 / Notices
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2022–11771 Filed 6–1–22; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60-Day–22–1083; Docket No. CDC–2022–
0071]

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 Extended
Evaluation of the National Tobacco
Prevention and Control Public
Education Campaign. This collection is
used to evaluate the Tips From Former
Smokers (Tips) campaign, which
encourages smokers to quit smoking and
to communicate with smokers about the
dangers of smoking.
DATES: CDC must receive written
comments on or before August 1, 2022.
ADDRESSES: You may submit comments,
identified by Docket No. CDC–2022–
0071 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

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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
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
Extended Evaluation of the National
Tobacco Prevention and Control Public
Education Campaign (OMB Control No.
0920–1083, Exp. 03/31/2023)—
Revision—National Center for Chronic
Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
In 2012, HHS/CDC launched the
National Tobacco Prevention and

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33491

Control Public Education Campaign,
Tips From Former Smokers (Tips)
campaign. The primary objectives of the
Tips campaign are to encourage smokers
to quit smoking and to encourage
nonsmokers to communicate with
smokers about the dangers of smoking.
Tips airs annually in all U.S. media
markets on broadcast and national cable
TV as well as other media channels
including digital video, online display
and banners, radio, billboards, and other
formats. Tips ads rely on evidencebased paid media advertising that
highlights the negative health
consequences of smoking. Tips primary
target audience is adult smokers; adult
nonsmokers constitute the secondary
audience. Tips paid advertisements are
aimed at providing motivation and
support to smokers to quit, with
information and other resources to
increase smokers’ chances of success in
their attempts to quit smoking. A key
objective for the nonsmoker audience is
to encourage nonsmokers to
communicate with smokers they may
know (including family and friends)
about the dangers of smoking and to
encourage them to quit. Tips ads also
focus on increasing audience’s
knowledge of smoking-related diseases,
intentions to quit, and other related
outcomes.
The goal of the proposed information
collection is to evaluate the reach of the
Tips campaign among intended
audiences and to examine the
effectiveness of these efforts in
impacting specific outcomes that are
targeted by Tips, including quit
attempts and intentions to quit among
smokers, nonsmokers’ communications
about the dangers of smoking, and
knowledge of smoking-related diseases
among both audiences. This will require
customized surveys that will capture all
unique messages and components of
Tips. Information will be collected
through Web-based surveys to be selfadministered by adults 18 and over on
computers in the respondent’s home or
in another convenient location.
Evaluating the impact of the Tips
campaign on behavioral outcomes is
necessary to determine campaign cost
effectiveness and to allow program
planning for the most effective
campaign outcomes. Because Tips
content changes, it is necessary to
evaluate each yearly implementation of
the Tips campaign.
The proposed information collection
will include three survey collections per
year (nine surveys in total) generally
conducted before, during, and after the
Tips campaign in each year. Using the
same methods outlined in the currently
approved information collection (OMB

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Federal Register / Vol. 87, No. 106 / Thursday, June 2, 2022 / Notices

Control No. 0920–1083, Exp. 3/31/
2023), participants will be recruited
from two sources: (1) An online
longitudinal cohort of adult smokers
and nonsmokers, sampled randomly
from postal mailing addresses in the
United States (address-based sample, or
ABS); and (2) the existing GfK/Ipsos
KnowledgePanel, an established longterm online panel of U.S. adults. All
online surveys, regardless of sample
source, will be conducted via the GfK/
Ipsos KnowledgePanel Web portal for
self-administered surveys.
Information collected by these
surveys include smokers’ and

nonsmokers’ awareness of and exposure
to specific Tips advertisements;
knowledge, attitudes, beliefs related to
smoking and secondhand smoke; and
other marketing exposures. The surveys
will also measure behaviors related to
smoking cessation (among the smokers
in the sample) and behaviors related to
nonsmokers’ encouragement of smokers
to quit smoking, recommendations of
cessation services, and attitudes about
other tobacco and nicotine products.
It is important to evaluate the Tips
campaign in a context that assesses the
dynamic nature of tobacco product
marketing and uptake of various tobacco

products, particularly since these may
affect successful cessation rates. Survey
instruments may be updated to include
new or revised items on relevant topics,
including cigars, noncombustible
tobacco products, and other emerging
trends in tobacco use.
The total response burden is
estimated at 9,308 annual hours.
Approval is requested for three years
between early fall 2023 and December
2026. Participation is voluntary and
there are no costs to respondents other
than their time.

ESTIMATED ANNUALIZED BURDEN HOURS
Average
burden per
response
(in hours)

Total burden
(in hours)

Form name

General Population ...........................
Adult Smokers, ages 18–54, in the
United States.

Screening & Consent .......................
Smoker Survey Wave A ...................

16,667
2,668

1
1

5/60
20/60

1,389
889

Smoker Survey Wave B ...................
Smoker Survey Wave C ..................
Smoker Survey Wave D ..................
Smoker Survey Wave E ...................
Smoker Survey Wave F ...................
Smoker Survey Wave G ..................
Smoker Survey Wave H ..................
Smoker Survey Wave I ....................
Nonsmoker Survey Wave A .............

1,667
1,667
1,667
1,667
1,667
1,667
1,667
1,667
1,100

1
1
1
1
1
1
1
1
1

20/60
20/60
20/60
20/60
20/60
20/60
20/60
20/60
20/60

556
556
556
556
556
556
556
556
366

B .............
C ............
D ............
E .............
F .............
G ............
H ............
I ..............

835
835
835
835
835
835
835
835

1
1
1
1
1
1
1
1

20/60
20/60
20/60
20/60
20/60
20/60
20/60
20/60

277
277
277
277
277
277
277
277

...........................................................

........................

........................

........................

9,308

Adult Nonsmokers, ages 18–54, in
the United States.

Nonsmoker
Nonsmoker
Nonsmoker
Nonsmoker
Nonsmoker
Nonsmoker
Nonsmoker
Nonsmoker
Total ...........................................

Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2022–11773 Filed 6–1–22; 8:45 am]
BILLING CODE 4163–18–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifiers: CMS–10779]
jspears on DSK121TN23PROD with NOTICES1

Number of
responses per
respondent

Number of
respondents

Type of respondents

Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).

AGENCY:

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Notice.

The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995
(PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, and to allow
a second opportunity for public
comment on the notice. Interested
persons are invited to send comments
regarding the burden estimate or any
other aspect of this collection of
information, including the necessity and
utility of the proposed information
collection for the proper performance of
the agency’s functions, the accuracy of

SUMMARY:

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the estimated burden, ways to enhance
the quality, utility, and clarity of the
information to be collected, and the use
of automated collection techniques or
other forms of information technology to
minimize the information collection
burden.
Comments on the collection(s) of
information must be received by the
OMB desk officer by July 5, 2022.
ADDRESSES: Written comments and
recommendations for the proposed
information collection should be sent
within 30 days of publication of this
notice to www.reginfo.gov/public/do/
PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function.
To obtain copies of a supporting
statement and any related forms for the
DATES:

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