[Federal Register Volume 78, Number 220 (Thursday, November 14, 2013)]
[Notices]
[Pages 68450-68451]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2013-27274]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
[30Day-14-13QQ]
Proposed Data Collections Submitted for Public Comment and
Recommendations
In compliance with the requirement of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995 for opportunity for public comment on
proposed data collection projects, the Centers for Disease Control and
Prevention (CDC) will publish periodic summaries of proposed projects.
To request more information on the proposed projects or to obtain a
copy of the data collection plans and instruments, call 404-639-7570
and send comments to Kimberly S. Lane, 1600 Clifton Road, MS-D74,
Atlanta, GA 30333 or send an email to [email protected].
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; and (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. Written comments should be received
within 30 days of this notice.
Proposed Project
Older Adult Safe Mobility Assessment Tool--NEW--National Center for
Injury Prevention and Control (NCIPC), Centers for Disease Control and
Prevention (CDC).
Background and Brief Description
In 2010, there were 40 million adults aged 65 or older in the U.S.,
representing 13% of the U.S. population. By 2030, this segment of the
population will increase to an estimated 72 million or 20%. People now
aged 65 are expected to live well into their 80s with the vast majority
preferring to ``age in place'' (i.e., grow old in their current homes).
With most adults aging in place, rather than in retirement or nursing
homes, it is absolutely critical to better prepare communities and
older Americans for what is on the horizon.
There is widespread agreement that older adults in the U.S. do not
adequately plan for their future mobility needs, nor are most aware of
existing mobility resources in their communities. Thus, when an
individual's mobility becomes impaired they are ill prepared to adapt
their lifestyle to their changing needs. A process of mobility
assessment would begin to address this situation and aid older adults
in meeting their changing mobility needs.
At present there are numerous mobility-related assessments actively
used throughout the U.S. Most are designed to collect information from
just one particular mobility silo, such as assessments that focus on
fall prevention. None of these existing tools cut across mobility silos
while focusing on older adults. None create a national picture of older
adult safe mobility that captures an individual's physical and
emotional health, their social network, or the ease of mobility in
their home, transportation, their neighborhood, their city, and beyond.
And no existing older adult tools are both mobility holistic and
empowerment driven self-administered assessments. The data collected in
this project will allow CDC to develop a Tool that can help older
adults both assess and improve their complete mobility.
This project involves developing, refining and validating a Safe
Mobility Assessment Tool that allows older adults to assess their
current mobility situation, learn about mobility challenges that may
affect them in the future, and receive actionable feedback on how to
improve and protect their mobility. The information collected in this
project will be used to refine and improve the Tool, as well as to
conduct feasibility and audience acceptability analysis of the Tool.
This information will allow CDC to create the most useful Safe Mobility
Assessment Tool possible for U.S. older adults.
CDC requests OMB approval for one year to collect both qualitative
and quantitative data in order to develop and refine the Tool, and
assess feasibility and audience acceptability. Qualitative data
collection will include key informant interviews, focus groups, and
intercepts in urban and rural communities. In brief, these methods will
include key informant interviews of community stakeholders (three
stakeholder interviews in two states for a total of six key informant
interviews); older adult consumer focus groups (two focus groups in two
states with seven people each for a total of fourteen participants);
and older adult consumer intercepts (thirty intercepts in two rural
locations and ten intercepts in two urban locations for a total of
forty intercepts). The qualitative data collection will be used to help
inform a quantitative stage of work to include a national sample of
geographically and socio-demographically diverse older adults (N =
1,000) who will be recruited and interviewed by telephone. The key
informant interviews, focus groups, intercepts and telephone survey
data collection will allow us to gain information about the feasibility
and usefulness of the Older Adult Safe Mobility Tool; about what
impacts the Tool may have on older adults (e.g., motivation to change/
behavior intent, and changes in knowledge, attitude, and awareness);
about which mobility domains are most valuable to include in the Tool
(e.g., which are of greatest
[[Page 68451]]
interest and can be improved by older adults), and about what other
areas of the Tool could be refined and improved. This information will
allow us to create a final version of the Safe Mobility Assessment Tool
that can be used by older adults across the U.S. to protect and enhance
their mobility.
CDC anticipates that data collection will begin in December 2013
and that all data collection will be completed by July 2014. CDC
estimates the following burden for one-time respondents: Key informant
interviews will be administered to 6 individuals and will take
approximately 30 minutes to complete for a total burden of 3 hours,
focus groups will be conducted for 14 older adults requiring up to 15
minutes per participant to review the consent form and screener and 120
minutes to participate in the focus group for a total burden of 32
hours, intercept interviews will be administered to 40 older adults
requiring up to 15 minutes to review the consent and screener form and
30 minutes to participate in the interview for a total burden of 30
hours, and the telephone survey will survey 1000 older adults involving
an on-your-own review of materials (approximately 15 minutes) and a
pre-scheduled telephone survey (approximately 27 minutes) for a total
burden of 700 hours.
Key informant interviews and the quantitative survey will be
conducted by telephone. As telephone survey participants are recruited,
they may elect to receive stimulus material (i.e., a draft version of
the Tool) prior to the survey either by mail or electronically via
email, whichever they prefer. In addition, focus group participants may
receive communications (confirmation and reminder notices) via email or
mail. Email communication will be used with key informant, focus group
and telephone survey respondents, however each will be given the option
of mail rather than email as their preferred communication method.
Email will be provided not only as a courtesy to respondents, for those
respondents that prefer email rather than mail, but also, it will allow
more open and swift communication between CDC and the study
participants. Additionally, recruitment/screening for the focus groups
and telephone surveys, as well as administration of the telephone
surveys will use Computer Assisted Telephone Interview (CATI) systems
for data collection, which are designed to reduce the burden to
respondents.
There are no costs to respondents other than their time. The total
estimated annual burden hours are 765.
Estimate Annualized Burden Hours
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Number of Response
Type of respondent Form name Number of responses per burden (in
respondents respondent hours)
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Key informant interview respondents... Interview guide......... 6 1 30/60
Focus group respondents............... Respondent Consent & 14 1 15/60
Screener.
Moderator guide......... 14 1 2
Intercept respondents................. Respondent Consent & 40 1 15/60
Screener.
Intercept script........ 40 1 30/60
Telephone survey respondents.......... Respondent Consent & 1000 1 15/60
Screener.
Survey.................. 1,000 1 27/60
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Kimberly S. Lane,
Deputy Director, Office of Science Integrity, Office of the Associate
Director for Science, Office of the Director, Centers for Disease
Control and Prevention.
[FR Doc. 2013-27274 Filed 11-13-13; 8:45 am]
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