Att 2a. Federal Register Notice

Att 2a. Federal Register Notice.pdf

Message Testing for Tobacco Communication Activities

Att 2a. Federal Register Notice

OMB: 0920-0910

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46829

Federal Register / Vol. 79, No. 154 / Monday, August 11, 2014 / Notices
ESTIMATE OF ANNUALIZED BURDEN HOURS—Continued
Number of
respondents

Type of respondents—state epidemiologists

Human Infection with Novel Influenza A Virus Case Report Form .............................................
Human Infection with Novel Influenza A Virus with Suspected Avian Source ...........................
Human Infection with Novel Influenza A Virus Severe Outcomes ..............................................
Novel Influenza A Virus Infection Contact Tracing Form ............................................................
Novel Influenza A Virus Case Status Summary .........................................................................
Novel Influenza A Virus Case Screening Form ..........................................................................
122 CMRS—City health officers or vital statistics registrars Daily Mortality Report ...................
122 CMRS—City health officers or vital statistics registrars Weekly Mortality Report ...............
Aggregate Hospitalization and Death Reporting Activity Weekly Report Form ..........................
Antiviral Resistant Influenza Infection Case Report Form ..........................................................
National Respiratory & Enteric Virus Surveillance System (NREVSS) (CDC 55.83 Lab Assessment Form, 55.83A, B, D) (electronic) .............................................................................
National Enterovirus Surveillance Report: (CDC 55.9) (electronic) ............................................
Adenovirus Typing Report Form .................................................................................................
Middle East Respiratory Syndrome Coronavirus (MERS) Patient Under Investigation (PUI)
Form .........................................................................................................................................
Form for Submitting Specimens From Suspected Norovirus Outbreaks ....................................
Waterborne Disease Transmission CDC 52.12 ..........................................................................
Influenza Virus (Electronic, Year Round), PHLIP_HL7 messaging Data Elements ...................
-Influenza virus (electronic, year round) (PHIN–MS) ..................................................................

Leroy Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
[FR Doc. 2014–18844 Filed 8–8–14; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[60Day–14–0910]

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Proposed Data Collections Submitted
for Public Comment and
Recommendations
The Centers for Disease Control and
Prevention (CDC), as part of its
continuing effort to reduce public
burden, invites the general public and
other Federal agencies to take this
opportunity to comment on proposed
and/or continuing information
collections, as required by the
Paperwork Reduction Act of 1995. To
request more information on the below
proposed project or to obtain a copy of
the information collection plan and
instruments, call 404–639–7570 or send
comments to Leroy Richardson, 1600
Clifton Road, MS–D74, Atlanta, GA
30333 or send an email to [email protected].
Comments submitted in response to
this notice will be summarized and/or
included in the request for Office of
Management and Budget (OMB)
approval. Comments are invited on: (a)

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Whether the proposed collection of
information is necessary for the proper
performance of the functions of the
agency, including whether the
information shall have practical utility;
(b) the accuracy of the agency’s estimate
of the burden of the proposed collection
of information; (c) ways to enhance the
quality, utility, and clarity of the
information to be collected; (d) ways to
minimize the burden of the collection of
information on respondents, including
through the use of automated collection
techniques or other forms of information
technology; and (e) estimates of capital
or start-up costs and costs of operation,
maintenance, and purchase of services
to provide information. Burden means
the total time, effort, or financial
resources expended by persons to
generate, maintain, retain, disclose or
provide information to or for a Federal
agency. This includes the time needed
to review instructions; to develop,
acquire, install and utilize technology
and systems for the purpose of
collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information, to search
data sources, to complete and review
the collection of information; and to
transmit or otherwise disclose the
information. Written comments should
be received within 60 days of this
notice.
Proposed Project
Message Testing for Tobacco
Communication Activities (OMB No.

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Number of
responses per
respondent

Average
burden per
response
(in hours)

57
57
57
57
57
57
58
122
56
57

6
1
1
1
1
1
365
52
52
3

30/60
30/60
1.5/60
30/60
15/60
15/60
12/60
12/60
10/60
30/60

300
25
25

52
12
12

15/60
15/60
15/60

57
20
57
49
3

3
5
1
52
52

25/60
15/60
20/60
5/60
5/60

0920–0910, exp. 1/31/2015)—
Revision—National Center for Chronic
Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
Background and Brief Description
In 2012, CDC’s Office on Smoking and
Health obtained OMB approval of a
generic clearance that established a
unified information collection
framework for the development of
tobacco-related health messages,
including messages related to CDC’s
ACA-funded tobacco education
campaign (Message Testing for Tobacco
Communication Activities (MTTCA),
OMB No. 0920–0910, exp. 1/31/2015).
The MTTCA clearance was initially
approved with the following estimates:
14,974 annualized responses and 5,775
annualized burden hours. On January 2,
2014, CDC obtained OMB approval to
increase the capacity of the MTTCA
clearance to 36,847 annualized
responses and 7,219 burden hours.
CDC has employed the MTTCA
clearance to collect information about
adult smokers’ and nonsmokers’
attitudes and perceptions, and to pretest draft messages and materials for
clarity, salience, appeal, and
persuasiveness. A variety of information
collection strategies are supported
through this mechanism, including indepth interviews, in-person focus
groups, online focus groups, computerassisted, in-person, or telephone
interviews, and online surveys. CDC
requests OMB approval for each data
collection by submitting a project-

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Federal Register / Vol. 79, No. 154 / Monday, August 11, 2014 / Notices

specific request that describes project
purpose, use, and methodology.
CDC plans to request OMB approval
to extend the MTTCA clearance, with
changes, for three years. The Revision
information collection request (ICR) will
propose further increases in the
annualized estimated number of
respondents and the annualized
estimated burden hours. These increases
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
(FDA), the Substance Abuse and Mental
Health Services Administration
(SAMHSA), the National Institutes of
Health (NIH), and the National Cancer
Institute (NCI). At this time the MTTCA
clearance is expected to be sufficient to
test tobacco related messages developed
by CDC. However, the MTTCA
clearance should not replace the need
for additional generic clearance

Finally, there may be a need to test
prevention and cessation messages
related to products that are not currently
regulated, including non-combustible
tobacco products (electronic nicotine
delivery systems such as electronic
cigarettes or e-cigarettes) and some
combustible products (such as cigars/
little cigars and cigarillos). In the event
that the FDA receives authority to
regulate these products and decides to
do a campaign about them, CDC will
work closely with FDA to avoid
duplication. Additionally, CDC will
share with FDA the findings from any
formative work related to the youth
audience.
CDC will continue to use the MTTCA
clearance to develop and test messages
and materials for current and future
phases of the ACA-funded media
campaign, OSH’s ongoing programmatic
initiatives including, but not limited to,
the Media Campaign Resource Center,
reports from the Office of the Surgeon
General, and other communication
efforts and materials. Participation is
voluntary and there are no costs to
respondents other than their time.

mechanisms HHS and other federal
partners may need to test tobacco
messages related to their campaigns and
initiatives.
CDC’s revised MTTCA clearance will
also describe expansion of the target
audience(s) that may be involved in
message testing, such as youth ages 13–
17 years. The 2014 Surgeon General’s
Report concluded that there is already
sufficient evidence to caution youth
against the use of electronic cigarettes.
Tobacco and electronic cigarette
advertising and promotional activities
can prompt smoking initiation,
especially among youth. Recent studies
have found that 90.7% of middle school
students and 92.9% of high school
students have been exposed to protobacco advertisements in stores,
magazines and on the internet. Media
campaigns have been shown to be
effective as part of a comprehensive
tobacco control program to decrease the
initiation of tobacco use among youths
and young adults. A coordinated series
of health message testing activities will
be required to support future
development of effective, audiencespecific and channel-specific messages
for CDC’s ACA-funded campaign.

ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent

Number of
respondents

Total burden
(in hours)

Form name

General Public and Special Populations.

Screening and Recruitment .................................

20,000

1

2/60

667

In-depth Interviews (In Person, telephone, etc.)
Focus Groups (In Person) ...................................
Focus Groups (Online) ........................................
Short Surveys/information needed to screen individuals being considered for inclusion in
campaign ads (Online, Bulletin Board, etc.).
Medium Surveys (Online) ....................................
In-depth Surveys (Online) ...................................

96
160
120
9,800

1
1
1
1

1
1.5
1
10/60

96
240
120
1,633

9,940
4,100

1
1

25/60
1

4,142
4,100

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

44,216

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

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

10,998

Total ........................

Leroy Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

[FR Doc. 2014–18902 Filed 8–8–14; 8:45 am]

[CMS–3300–NC]

Centers for Medicare & Medicaid
Services

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Average
burden per
response
(in hours)

Type of respondents

Medicare Program; Evaluation Criteria
and Standards for Quality
Improvement Networks Quality
Improvement Program Contracts [Base
and Task Order(s)]
Centers for Medicare &
Medicaid Services (CMS), HHS.

AGENCY:

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ACTION:

Notice with comment period.

This notice with comment
period describes the general criteria we
intend to use to evaluate the
effectiveness and efficiency of the
Quality Innovation Network (QIN)
Quality Improvement Organizations
(QIOs) that will enter into contracts
with CMS under the Quality Innovation
Network Quality Improvement
Organizations (Solicitation Number:
HHSM–500–2014–RFP–QIN–QIO)
Statement of Work (SOW) on August 1,
2014. The evaluation of a QIN–QIO’s
performance related to their SOW will
be based on evaluation criteria specified
for the tasks and subtasks set forth in

SUMMARY:

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