Proposed Data Collections Submitted for Public Comment and Recommendations, 10095-10096 [2015-03825]

Download as PDF 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

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