Agency Information Collection Activities; Submission for OMB Review; Public Comment Request; of the Evaluation of the National Paralysis Resource Center (NPRC) and Performance Management Support OMB Control Number 0985-New
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Abstract
The Administration for Community Living is announcing that the proposed collection of information listed above has been submitted to the Office of Management and Budget (OMB) for review and clearance as required under the Paperwork Reduction Act of 1995. This 30-day notice collects comments on the information collection requirements related to the Evaluation of the National Paralysis Resource Center (NPRC) and Performance Management Support.
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<title>Federal Register, Volume 88 Issue 36 (Thursday, February 23, 2023)</title>
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[Federal Register Volume 88, Number 36 (Thursday, February 23, 2023)]
[Notices]
[Pages 11446-11447]
From the Federal Register Online via the Government Publishing Office [<a href="http://www.gpo.gov">www.gpo.gov</a>]
[FR Doc No: 2023-03740]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Community Living
Agency Information Collection Activities; Submission for OMB
Review; Public Comment Request; of the Evaluation of the National
Paralysis Resource Center (NPRC) and Performance Management Support OMB
Control Number 0985-New
AGENCY: Administration for Community Living, HHS.
ACTION: Notice.
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SUMMARY: The Administration for Community Living is announcing that the
proposed collection of information listed above has been submitted to
the Office of Management and Budget (OMB) for review and clearance as
required under the Paperwork Reduction Act of 1995. This 30-day notice
collects comments on the information collection requirements related to
the Evaluation of the National Paralysis Resource Center (NPRC) and
Performance Management Support.
DATES: Submit written comments on the collection of information by
March 27, 2023.
ADDRESSES: Submit written comments and recommendations for the proposed
information collection within 30 days of publication of this notice to
<a href="http://www.reginfo.gov/public/do/PRAMain">www.reginfo.gov/public/do/PRAMain</a>. Find the information collection by
selecting ``Currently under 30-day Review--Open for Public Comments''
or by using the search function. By mail to the Office of Information
and Regulatory Affairs, OMB, New Executive Office Bldg., 725 17th St.
NW, Rm. 10235, Washington, DC 20503, Attn: OMB Desk Officer for ACL.
FOR FURTHER INFORMATION CONTACT: Amanda Cash, 202-795-7369 or
<a href="/cdn-cgi/l/email-protection#563320373a2337223f39381637353a783e3e2578313920"><span class="__cf_email__" data-cfemail="513427303d243025383e3f1130323d7f3939227f363e27">[email protected]</span></a>.
SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, ACL has
submitted the following proposed collection of information to OMB for
review and clearance. The Administration for Community Living (ACL) is
requesting approval to collect data for the National Paralysis Resource
Center (NPRC) to understand how and to what extent the NPRC is meeting
its goals. The NPRC provides resources to people living with paralysis,
their caregivers, and their support network. ACL is responsible for
oversight of the NPRC, which has been administered by the Christopher
and Dana Reeve Foundation since its authorization in 2009. This data
collection effort will be focused on evaluating specific major
activities of the NPRC: (a) the Quality of Life (QOL) Grants Program;
(b) the Peer and Family Support Program (PFSP); and (c) the Promotional
Activities, Outreach, and Collaboration program.
This evaluation seeks to identify barriers and challenges to
operating the NPRC, document best practices for other Resource Centers,
and recommend areas for improvement.
Specifically, this IC will help ACL to understand how each major
NPRC activity aims to achieve the following goals, and to what extent
the activities affect related outcomes:
a. Improving the health and quality of life of individuals living
with paralysis of all ages, their families, and their support network;
b. Raising awareness of members of the target populations about
paralysis;
c. Increasing access of members of the target populations to
services relevant to individuals with paralysis;
d. Increasing the empowerment, confidence, and independence of
individuals living with paralysis;
e. Strengthening support networks for individuals living with
paralysis; and
f. Improving and increasing opportunities for community living for
individuals living with paralysis and their caretakers.
To gain an in-depth understanding of the perspectives of mentors
and peers participating in the PFSP, QOL program subgrantees, and
people who serve as regional champions in the Promotional Activities,
Outreach, and Collaboration program, eight focus groups will be
conducted with no more than eight people per focus group. Additionally,
a web-based survey will be administered to a maximum of 400 PFSP peers,
180 PFSP mentors, and 300 people served by QOL subgrantees to
understand respondents' experiences with the NPRC.
This data will contribute to documenting how each of the NPRC's
major activities are delivered and the extent to which they improve the
quality of life of people living with paralysis, their caregivers, and
their support networks.
Findings can inform practice for the NPRC and other Resource
Centers. This evaluation will also help to identify how the NPRC can
better meet the stated goals of the Department of Health and Human
Services (HHS) to, ``protect and strengthen equitable access to high
quality and affordable healthcare,'' and to, ``strengthen social well-
being, equity, and economic resilience.'' \1\
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\1\ FY 2023 Evaluation Plan (p. 3). (2022). U.S. Department of
Health & Human Services. <a href="https://aspe.hhs.gov/reports/fy-2023-hhs-evaluation-plan">https://aspe.hhs.gov/reports/fy-2023-hhs-evaluation-plan</a>.
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[[Page 11447]]
Comments in Response to the 60-Day Federal Register Notice
A notice published in the Federal Register Vol. 87, No. 207 pages
65068-65069 on October 27, 2022. No public comments were received
during the 60-day FRN.
Estimated Program Burden: ACL estimates the burden of this
collection of information as follows:
The eight focus groups together will include no more than 64 total
individuals representing three major activities of the NPRC: the QOL
Grants Program; the PFSP; and the Promotional Activities, Outreach, and
Collaboration program. The burden for their participation is estimated
at 1.5 hours per participant, for a total of 96 hours.
A maximum of 180 PFSP mentors, 400 PFSP peers, and 300 people
served by QOL subgrantee programs are expected to respond to the web-
based survey, for a total of 880 respondents. The approximate burden
for survey completion is 15 minutes for the peer mentor survey, and 10
minutes for the peer survey and QOL end-user survey per respondent. In
addition, an estimated 5 minute non-response survey will be
administered to the PFSP mentors and PFSP peers who did not respond to
the web-based survey.
This results in a total survey burden estimate of 14,050 minutes
(234.17 hours). The estimated survey completion burden includes time to
review the instructions, read the questions, and complete responses.
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Number of Responses per Annual burden Annual burden
Data collection form Respondent type respondents respondent Hours per response hours * Cost per hour cost
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Focus group--Quality of Life Private sector-- 24 1 1.50.................... 36 \1\ $45.01 $1,620.36
organizational business, non-
representatives. profit, or
local
government.
Focus group--Peer Mentors... Individual..... 16 1 1.50.................... 24 \2\ 28.01 672.24
Focus group--Peer Mentees... Individual..... 16 1 1.50.................... 24 \2\ 28.01 672.24
Focus group--Regional Individual..... 8 1 1.50.................... 12 \2\ 28.01 336.12
Champions.
Survey--Peer Mentor......... Individual..... 180 1 0.25.................... 45 \2\ 28.01 1,260.45
Survey--Peers............... Individual..... 400 1 0.17.................... 68 \2\ 28.01 1,904.68
Survey--Quality of Life End- Individual..... 300 1 0.17.................... 51 \2\ 28.01 1,428.51
User.
Survey--Non-response follow- Individual..... 85 1 0.08.................... 6.8 \2\ 28.01 190.47
up (Peer Mentor).
Survey--Non-response follow- Individual..... 230 1 0.08.................... 18.4 \2\ 28.01 515.38
up (Peers).
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Total................... ............... 1,259 ............... .23 (weighted mean)..... 285.2 .............. 8,600.45
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* This is maximum number of hours for year one of data collection which is the largest year for data collection.
\1\ Bureau of Labor Statistics, Mean hourly wage for Social and Community Service Managers, May 2021 National Occupational Employment and Wage Estimates
by ownership, Local government, including schools and hospitals, <a href="https://www.bls.gov/oes/current/999301.htm#21-0000">https://www.bls.gov/oes/current/999301.htm#21-0000</a>.
\2\ Bureau of Labor Statistics, Mean hourly wage for All Occupations, May 2021 National Occupational Employment and Wage Estimates, United States,
<a href="https://www.bls.gov/oes/current/oes_nat.htm#00-0000">https://www.bls.gov/oes/current/oes_nat.htm#00-0000</a>.
* Annual burden hours were calculated from total minutes for each activity divided by sixty.
Dated: February 17, 2023.
Alison Barkoff,
Acting Administrator and Assistant Secretary for Aging.
[FR Doc. 2023-03740 Filed 2-22-23; 8:45 am]
BILLING CODE 4154-01-P
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