[Federal Register Volume 78, Number 73 (Tuesday, April 16, 2013)]
[Notices]
[Pages 22551-22552]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2013-08862]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-13-12EG]
Agency Forms Undergoing Paperwork Reduction Act Review
The Centers for Disease Control and Prevention (CDC) publishes a
list of information collection requests under review by the Office of
Management and Budget (OMB) in compliance with the Paperwork Reduction
Act (44 U.S.C. Chapter 35). To request a copy of these requests, call
the CDC Reports Clearance Officer at (404) 639-7570 or send an email to
[email protected]. Send written comments to CDC Desk Officer, Office of
Management and Budget, Washington, DC or by fax to (202) 395-5806.
Written comments should be received within 30 days of this notice.
Proposed Project
Use of Smartphones to Collect Information about Health Behaviors:
Feasibility Study--New--National Center for Chronic Disease Prevention
and Health Promotion (NCCDPHP), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
Despite the high level of public knowledge about the adverse
effects of smoking, tobacco use remains the leading preventable cause
of disease and death in the U.S., resulting in approximately 443,000
deaths annually. During 2005-2010, the overall proportion of U.S.
adults who were current smokers declined from 20.9% to 19.3%. Despite
this decrease, smoking rates are still well above Healthy People 2020
targets for reducing adult smoking prevalence to 12%, and the decline
in prevalence was not uniform across the population. Timely information
on tobacco usage is needed for the design, implementation, and
evaluation of public health programs.
New mobile communications technologies provide a unique opportunity
for innovation in public health surveillance. Text messaging and
smartphone Web access are immediate, accessible, and anonymous, a
combination of features that could make smartphones ideal for the
ongoing research, surveillance, and evaluation of risk behaviors and
health conditions, as well as targeted dissemination of information.
CDC proposes to conduct a feasibility study to evaluate the process
of conducting Web surveys by smartphone
[[Page 22552]]
and text message surveys by feature phone (cell phones that do not have
Web access), the outcomes of the surveys, and the value of the surveys.
The universe for this study is English-speaking U.S. residents aged 18-
65. The sample frame will consist of a national random digit dial
sample of telephone numbers from a frame of known cell phone exchanges.
Respondents reached on their cell phones will be asked to complete an
initial CATI survey consisting of a short series of simple demographic
questions, general health questions, and questions about tobacco and
alcohol use. At the conclusion of this brief survey, respondents who
have smartphones will be asked to participate in the feasibility study,
which consists of a first follow-up survey and, a week later, a second
follow-up survey. Those who agree will receive invitations to
participate by text message, which will include a link to the survey. A
sample of respondents who have feature phones will be asked to
participate in a text message pilot, which also consists of a first
follow-up survey and a second follow-up survey. Text message
respondents will receive a text message inviting them to participate;
respondents who opt in will receive text messages with one survey
question at a time. Before initiating the feasibility study, CDC will
conduct a brief pre-test of information collection forms and
procedures.
This study will evaluate: (1) Response bias of a smartphone health
survey by comparing data collected via CATI to data collected via
smartphones/text messages, and data collected via smartphones to data
collected via text messages, (2) relative cost-effectiveness of data
collected via CATI to data collected via smartphones/text messages; (3)
coverage bias associated with restricting the sample to smartphone
users; and (4) the utility of smartphones for completing frequent,
short interviews (e.g., diary studies to track activities or events).
OMB approval is requested for one year. Participation is voluntary.
There are no costs to respondents other than their time. The total
estimated annualized burden hours are 306.
Estimated Annualized Burden Hours
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Average
Number of Number of burden per
Type of respondents Form name respondents responses per response (in
respondent hr)
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Adults Aged 18 to 65, All cell phone Pre-test (CATI Screener/ 20 1 8/60
users. CATI Recruitment.
Screener/CATI 1,990 1 1/60
Recruitment.
Initial CATI Survey..... 1,590 1 7/60
Adults Aged 18 to 65, Smartphone Users First Web Survey Follow- 700 1 3/60
up for Smartphone Users.
Second Web Survey Follow- 595 1 3/60
up for Smartphone Users.
Adults Aged 18 to 65, Non-smartphone First Text Message 200 1 3/60
Users. Survey Follow-up for
non-Smartphone Users.
Second Text Message 170 1 3/60
Survey Follow-up for
non-Smartphone Users.
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Ron A. Otten,
Director, Office of Scientific Integrity, Office of the Associate
Director for Science, Office of the Director, Centers for Disease
Control and Prevention.
[FR Doc. 2013-08862 Filed 4-15-13; 8:45 am]
BILLING CODE 4163-18-P