Proposed Data Collections Submitted for Public Comment and Recommendations, 68450-68451 [2013-27274]
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68450
Federal Register / Vol. 78, No. 220 / Thursday, November 14, 2013 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Notice of Senior Executive Service
Performance Review Board
Membership
The Agency for Healthcare Research
and Quality (AHRQ) announces the
appointment of members to the AHRQ
Senior Executive Service (SES)
Performance Review Board (PRB). This
action is being taken in accordance with
5 U.S.C. 4314(c)(4), which requires
notice of appointment of members to
performance review boards to be
published in the Federal Register.
Members of the PRB are appointed in
a manner that will ensure consistency,
stability and objectivity in the SES
performance appraisals. The function of
the PRB is to make recommendations to
the Director, AHRQ, relating to the
performance of senior executives in the
Agency.
The following persons will serve on
the AHRQ SES Performance Review
Board:
Irene Fraser; Stephen B. Cohen; William
Munier; David Meyers; Michael
Fitzmaurice; Phyllis Zucker; Mark
Handelman; Jean Slutsky;
For further information about the
AHRQ Performance Review Board,
contact Ms. Alison Reinheimer, Office
of Management Services, Agency for
Healthcare Research and Quality, 540
Gaither Road, Suite 4010, Rockville,
Maryland 20850.
Dated: November 5, 2013.
Richard Kronick,
AHRQ Director.
[FR Doc. 2013–27169 Filed 11–13–13; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[30Day–14–13QQ]
TKELleY on DSK3SPTVN1PROD with NOTICES
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
VerDate Mar<15>2010
19:20 Nov 13, 2013
Jkt 232001
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 omb@
cdc.gov.
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
PO 00000
Frm 00041
Fmt 4703
Sfmt 4703
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 selfadministered 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
E:\FR\FM\14NON1.SGM
14NON1
68451
Federal Register / Vol. 78, No. 220 / Thursday, November 14, 2013 / Notices
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
Number of
respondents
Type of respondent
Form name
Key informant interview respondents .............
Focus group respondents ...............................
Interview guide ...............................................
Respondent Consent & Screener ..................
Moderator guide .............................................
Respondent Consent & Screener ..................
Intercept script ................................................
Respondent Consent & Screener ..................
Survey ............................................................
Intercept respondents .....................................
Telephone survey respondents ......................
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.
DC 20503 or by fax to (202) 395–5806.
Written comments should be received
within 30 days of this notice.
[FR Doc. 2013–27274 Filed 11–13–13; 8:45 am]
Generic Clearance for the Collection
of Qualitative Feedback on Agency
Service Delivery—NEW—Centers for
Disease Control and Prevention (CDC),
Office of the Associate Director for
Communication (OADC).
As part of a Federal Government-wide
effort to streamline the process to see
feedback from the public on service
delivery, the CDC has submitted a
Generic Information Collection Request
(Generic ICR): ‘‘Generic Clearance for
the Collection of Qualitative Feedback
on Agency Service Delivery’’ to OMB for
approval under the Paperwork
Reduction Act (PRA) (44 U.S.C. 3501 et.
Seq.).
To request additional information,
please contact Kimberly S. Lane,
Centers for Disease Control and
Prevention, 1600 Clifton Road, MS–D74,
Atlanta, GA 30333 or send an email to
omb@cdc.gov.
Proposed Project
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DEPARTMENT OF HEALTH AND
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Centers for Disease Control and
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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 (404) 639–7570 or send an
email to omb@cdc.gov. Send written
comments to CDC Desk Officer, Office of
Management and Budget, Washington,
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Jkt 232001
SUPPLEMENTARY INFORMATION:
PO 00000
Frm 00042
Fmt 4703
Sfmt 4703
6
14
14
40
40
1000
1,000
Number of
responses
per
respondent
Response
burden
(in hours)
1
1
1
1
1
1
1
30/60
15/60
2
15/60
30/60
15/60
27/60
Title: Generic Clearance for the
Collection of Qualitative Feedback on
Agency Service Delivery.
Abstract: The information collection
activity will garner qualitative customer
and stakeholder feedback in an efficient,
timely manner, in accordance with the
Administration’s commitment to
improving service delivery. By
qualitative feedback we mean
information that provides useful
insights on perceptions and opinions,
but are not statistical surveys that yield
quantitative results that can be
generalized to the population of study.
This feedback will provide insights into
customer or stakeholder perceptions,
experiences and expectations, provide
an early warning of issues with service,
or focus attention on areas where
communication, training or changes in
operations might improve delivery of
products or services. These collections
will allow for ongoing, collaborative and
actionable communications between the
Agency and its customers and
stakeholders. It will also allow feedback
to contribute directly to the
improvement of program management.
Feedback collected under this generic
E:\FR\FM\14NON1.SGM
14NON1
Agencies
[Federal Register Volume 78, Number 220 (Thursday, November 14, 2013)]
[Notices]
[Pages 68450-68451]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-27274]
-----------------------------------------------------------------------
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 omb@cdc.gov.
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
----------------------------------------------------------------------------------------------------------------
Number of Response
Type of respondent Form name Number of responses per burden (in
respondents respondent hours)
----------------------------------------------------------------------------------------------------------------
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
----------------------------------------------------------------------------------------------------------------
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]
BILLING CODE 4163-18-P