Proposed Data Collections Submitted for Public Comment and Recommendations, 10095-10096 [2015-03825]
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10095
Federal Register / Vol. 80, No. 37 / Wednesday, February 25, 2015 / Notices
strengthen relationships between public
health and clinical care.
These activities will facilitate the
quick and efficient identification of
cases in future outbreaks and protect the
health and safety of patients. This
request corresponds with an initial
ongoing data collection (Phase I), State
Health Department Access to Electronic
Health Record Data during an Outbreak:
A Retrospective Assessment, which
involves interviews with four types of
Health Department staff: Healthcareassociated infection coordinator,
epidemiologist, legal counsel, and
informatics director (OMB Number
0920–0879, approved on 04/24/2014).
Phase I data analysis is ongoing.
For Phase II of this study, we will be
requesting participation from hospital
and clinic staff in their official
capacities across the same 15 states
included in the Phase I request. The
investigation. In hospitals, the
evaluation team will be conducting
interviews with staff members serving
in one of three roles: Infection
preventionist, informatics director, and
other as referred (e.g. privacy officer,
risk management, etc.). In clinics, the
evaluation team will be conducting
interviews with the clinic director, and
other as referred (e.g. patient records
manager, etc.)
The maximum estimates for burden
hours are derived from interview guide
pilot testing and data collection with
HDs during Phase I data collection, in
which interviews took 27 minutes. The
total annual burden is 90 hours.
The data to be collected do not
involve questions of a personal or
sensitive nature and should have no
impact on the individual’s privacy.
There are no costs to the respondents
other than their time.
states chosen for Phase I and Phase II
data collections are: Florida, Indiana,
Kansas, Maryland, Michigan,
Minnesota, New Hampshire, New
Jersey, New York, North Carolina, Ohio,
Oregon, Tennessee, Texas, and Virginia.
Data will be collected from 150 hospital
and clinic staff in their official
capacities using one 30-minute
telephone interview per person and
limiting interviews to two hospitals and
two clinics per state. Hospital
participants include: Infection
preventionists, informatics directors,
and others as referred. Clinic
participants include: Clinic directors
and others as referred.
The focus of this OMB request is to
conduct interviews with 150 healthcare
facilities’ staff, hospitals and clinics, in
their official capacity who has been
asked by HDs to provide access to their
EHRs during an HAI outbreak
ESTIMATED ANNUALIZED BURDEN HOURS
Number of respondents
Number of
responses per
respondent
..............................................
..............................................
..............................................
..............................................
15
30
30
30
1
1
1
1
Interview Guide ..............................................
Interview Guide ..............................................
30
30
Form name
HD Epidemiologist ..........................................
Infection Preventionist ....................................
Informatics Director .........................................
Other as referred by Infection Preventionist
or Informatics Director (for example, privacy officer or risk management specialist).
Clinic Director .................................................
Other as referred by Clinic Director (for example, patient records manager).
Leroy A. 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. 2015–03805 Filed 2–24–15; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
asabaliauskas on DSK5VPTVN1PROD with NOTICES
[60 Day–15–15PI]
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 and maximize the utility of
government information, invites the
general public and other Federal
agencies to take this opportunity to
VerDate Sep<11>2014
18:05 Feb 24, 2015
Jkt 235001
Average
burden per
response
(in hours)
1
1
Type of respondent
Interview
Interview
Interview
Interview
Guide
Guide
Guide
Guide
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 A. Richardson, 1600
Clifton Road, MS–D74, Atlanta, GA
30333 or send an email to omb@cdc.gov.
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)
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
PO 00000
Frm 00052
Fmt 4703
Sfmt 4703
60/60
30/60
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.
E:\FR\FM\25FEN1.SGM
25FEN1
10096
Federal Register / Vol. 80, No. 37 / Wednesday, February 25, 2015 / Notices
Proposed Project
Extended Evaluation of the National
Tobacco Prevention and Control Public
Education Campaign—New—National
Center for Chronic Disease Prevention
and Health Promotion (NCCDPHP),
Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
In 2012, Centers for Disease Control
and Prevention (CDC) launched the first
federally funded, national mass media
campaign to educate consumers about
the adverse health consequences of
tobacco use (the National Tobacco
Prevention and Control Public
Education Campaign, or ‘‘The
Campaign’’). The Campaign continued
in 2013 and 2014 with advertisements
known as ‘‘Tips from Former Smokers.’’
Activities for Phase 3 of the campaign
are ongoing. To assess the impact of The
Campaign in Phases 1–3, CDC obtained
OMB approval to conduct a series of
longitudinal surveys of smokers and
nonsmokers (OMB Control Number
0920–0923, exp. 3/31/2017).
New media activities for Phases 4 and
5 of The Campaign are scheduled to
launch in March 2015. To support
evaluation of The Campaign through
Phase 5, CDC plans to field four new
waves of information collection. The
surveys will be fielded in English and
Information will be collected through
Web surveys to be self-administered on
computers in the respondents’ homes or
in another convenient location.
Information will be collected about
smokers’ and nonsmokers’ awareness of
and exposure to specific campaign
advertisements; knowledge, attitudes,
beliefs related to smoking and
secondhand smoke; and other marketing
exposure. 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
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.
OMB approval is requested for two
years. Participation is voluntary and
there are no costs to respondents other
than their time.
Spanish and will occur during late
2015, 2016, and early 2017. Once
enrolled in the first wave of data
collection, all participants will be recontacted for follow-up at subsequent
survey waves.
The sample for the data collection
will originate from two sources: (1) An
online longitudinal cohort of smokers
and nonsmokers, sampled randomly
from postal mailing addresses in the
United States (address-based sample, or
ABS); and (2) the existing GfK
KnowledgePanel, an established longterm online panel of U.S. adults. The
ABS-sourced longitudinal cohort will
consist of smokers and nonsmokers who
have not previously participated in any
established online panels to reduce
potential panel conditioning bias from
previous participation. The new cohort
will be recruited by GfK, utilizing
similar recruitment methods that are
used in the recruitment of
KnowledgePanel. The GfK
KnowledgePanel will be used in
combination with the new ABS-sourced
cohort to support larger sample sizes
that will allow for more in-depth
subgroup analysis, which is a key
objective for CDC. All online surveys,
regardless of sample source, will be
conducted via the GfK KnowledgePanel
Web portal for self-administered
surveys.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
(in hours)
Type of respondent
Form name
General Population ............................
Screening and Consent Questionnaire.
Smoker Survey (Wave A) ................
Smoker Survey (Wave B) ................
Smoker Survey (Wave C) ................
Smoker Survey (Wave D) ................
Nonsmoker Survey (Wave A) ..........
Nonsmoker Survey (Wave B) ..........
Nonsmoker Survey (Wave C) ..........
Nonsmoker Survey (Wave D) ..........
25,000
1
5/60
2,083
6,500
4,000
4,000
4,000
2,500
2,000
2,000
2,000
1
1
1
1
1
1
1
1
30/60
30/60
30/60
30/60
30/60
30/60
30/60
30/60
3,250
2,000
2,000
2,000
1,250
1,000
1,000
1,000
..........................................................
........................
........................
........................
15,583
Adults Smokers and Nonsmokers,
ages 18–54, in the United States.
asabaliauskas on DSK5VPTVN1PROD with NOTICES
Total ...........................................
Leroy A. 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. 2015–03825 Filed 2–24–15; 8:45 am]
[60Day–15–0824]
BILLING CODE 4163–18–P
Centers for Disease Control and
Prevention
Proposed Data Collections Submitted
for Public Comment and
Recommendations
The Centers for Disease Control and
Prevention (CDC), as part of its
VerDate Sep<11>2014
18:05 Feb 24, 2015
Jkt 235001
PO 00000
Frm 00053
Fmt 4703
Sfmt 4703
continuing effort to reduce public
burden and maximize the utility of
government information, 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
E:\FR\FM\25FEN1.SGM
25FEN1
]]>Agencies
[Federal Register Volume 80, Number 37 (Wednesday, February 25, 2015)]
[Notices]
[Pages 10095-10096]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2015-03825]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[60 Day-15-15PI]
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 and maximize the utility
of government information, 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 A.
Richardson, 1600 Clifton Road, MS-D74, Atlanta, GA 30333 or send an
email to omb@cdc.gov.
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) 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.
[[Page 10096]]
Proposed Project
Extended Evaluation of the National Tobacco Prevention and Control
Public Education Campaign--New--National Center for Chronic Disease
Prevention and Health Promotion (NCCDPHP), Centers for Disease Control
and Prevention (CDC).
Background and Brief Description
In 2012, Centers for Disease Control and Prevention (CDC) launched
the first federally funded, national mass media campaign to educate
consumers about the adverse health consequences of tobacco use (the
National Tobacco Prevention and Control Public Education Campaign, or
``The Campaign''). The Campaign continued in 2013 and 2014 with
advertisements known as ``Tips from Former Smokers.'' Activities for
Phase 3 of the campaign are ongoing. To assess the impact of The
Campaign in Phases 1-3, CDC obtained OMB approval to conduct a series
of longitudinal surveys of smokers and nonsmokers (OMB Control Number
0920-0923, exp. 3/31/2017).
New media activities for Phases 4 and 5 of The Campaign are
scheduled to launch in March 2015. To support evaluation of The
Campaign through Phase 5, CDC plans to field four new waves of
information collection. The surveys will be fielded in English and
Spanish and will occur during late 2015, 2016, and early 2017. Once
enrolled in the first wave of data collection, all participants will be
re-contacted for follow-up at subsequent survey waves.
The sample for the data collection will originate from two sources:
(1) An online longitudinal cohort of smokers and nonsmokers, sampled
randomly from postal mailing addresses in the United States (address-
based sample, or ABS); and (2) the existing GfK KnowledgePanel, an
established long-term online panel of U.S. adults. The ABS-sourced
longitudinal cohort will consist of smokers and nonsmokers who have not
previously participated in any established online panels to reduce
potential panel conditioning bias from previous participation. The new
cohort will be recruited by GfK, utilizing similar recruitment methods
that are used in the recruitment of KnowledgePanel. The GfK
KnowledgePanel will be used in combination with the new ABS-sourced
cohort to support larger sample sizes that will allow for more in-depth
subgroup analysis, which is a key objective for CDC. All online
surveys, regardless of sample source, will be conducted via the GfK
KnowledgePanel Web portal for self-administered surveys.
Information will be collected through Web surveys to be self-
administered on computers in the respondents' homes or in another
convenient location. Information will be collected about smokers' and
nonsmokers' awareness of and exposure to specific campaign
advertisements; knowledge, attitudes, beliefs related to smoking and
secondhand smoke; and other marketing exposure. 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 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.
OMB approval is requested for two years. Participation is voluntary
and there are no costs to respondents other than their time.
Estimated Annualized Burden Hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Type of respondent Form name respondents responses per response (in (in hours)
respondent hours)
--------------------------------------------------------------------------------------------------------------------------------------------------------
General Population............................. Screening and Consent Questionnaire.... 25,000 1 5/60 2,083
Adults Smokers and Nonsmokers, ages 18-54, in Smoker Survey (Wave A)................. 6,500 1 30/60 3,250
the United States. Smoker Survey (Wave B)................. 4,000 1 30/60 2,000
Smoker Survey (Wave C)................. 4,000 1 30/60 2,000
Smoker Survey (Wave D)................. 4,000 1 30/60 2,000
Nonsmoker Survey (Wave A).............. 2,500 1 30/60 1,250
Nonsmoker Survey (Wave B).............. 2,000 1 30/60 1,000
Nonsmoker Survey (Wave C).............. 2,000 1 30/60 1,000
Nonsmoker Survey (Wave D).............. 2,000 1 30/60 1,000
---------------------------------------------------------------
Total...................................... ....................................... .............. .............. .............. 15,583
--------------------------------------------------------------------------------------------------------------------------------------------------------
Leroy A. 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. 2015-03825 Filed 2-24-15; 8:45 am]
BILLING CODE 4163-18-P
