Agency Information Collection Activities: Proposed Collection; Public Comment Request; of the Office of Healthcare Information and Counseling (OHIC) Profiles at ACL OMB #0985-New, 65068-65069 [2022-23364]
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65068
Federal Register / Vol. 87, No. 207 / Thursday, October 27, 2022 / Notices
used, including aggregate data on
people served and program
development toward stated goals.
In this IC, the new quantitative grant
reporting tool will be disseminated to
all new Lifespan Respite Program
grantees upon grant award. Specifically,
the tool will collect information related
to respite care services delivered,
caregiver demographics, care recipient
demographics, respite training, and
lifespan respite program systems and
providers. Ultimately, this reporting
will assist ACL’s Office of Supportive
and Caregiver Services to assess the
performance of the Lifespan Respite
Program grantees in improving the
delivery and quality of respite services
for family caregivers of children and
adults of all ages with special needs.
The proposed data collection tools
may be found on the ACL website for
review at: https://www.acl.gov/aboutacl/public-input.
Estimated Program Burden: ACL
estimates the burden of this collection
of information as follows:
A maximum of 40 grantees are
expected to respond to the grant
reporting tool semiannually. The
approximate burden for completion may
be 6 hours per respondent for a total
estimate of 480 hours. The estimated
completion burden includes time to
review the instructions, read the
questions, compile information, and
complete responses.
IC BURDEN CHART
Respondent/data collection activity
Number of
respondents
Responses per
respondent
Hours per
response
Annual
burden hours
Grantee reporting tool ....................................................................................
40
2
6
480
........................
..........................
........................
480
Total ........................................................................................................
Dated: October 21, 2022.
Alison Barkoff,
Acting Administrator and Assistant Secretary
for Aging.
[FR Doc. 2022–23363 Filed 10–26–22; 8:45 am]
BILLING CODE 4154–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
Agency Information Collection
Activities: Proposed Collection; Public
Comment Request; of the Office of
Healthcare Information and Counseling
(OHIC) Profiles at ACL OMB #0985–
New
Administration for Community
Living, Department of Health and
Human Services.
ACTION: Notice.
AGENCY:
The Administration for
Community Living (ACL) is announcing
an opportunity for the public to
comment on the proposed collection of
information listed above. Under the
Paperwork Reduction Act of 1995
(PRA), Federal agencies are required to
publish a notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension of an existing collection of
information, and to allow 60 days for
public comment in response to the
notice. This is a new information
collection request soliciting comments
on the information collection
requirements relating to the Office of
Healthcare Information and Counseling
(OHIC) Profiles project at ACL.
DATES: Comments on the collection of
information must be submitted
khammond on DSKJM1Z7X2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
16:55 Oct 26, 2022
Jkt 259001
electronically by 11:59 p.m. (EST) or
postmarked by December 27, 2022.
ADDRESSES: Submit electronic
comments on the collection of
information to: Amanda Cash,
Amanda.Cash@acl.hhs.gov, 202–795–
7369. Submit written comments on the
collection of information to
Administration for Community Living,
330 C Street SW, Washington, DC
20201, Attention: Amanda Cash.
FOR FURTHER INFORMATION CONTACT:
Amanda Cash, Amanda.Cash@
acl.hhs.gov, 202–795–7369.
SUPPLEMENTARY INFORMATION: Under the
PRA (44 U.S.C. 3501–3520), Federal
agencies must obtain approval from the
Office of Management and Budget
(OMB) for each collection of
information they conduct or sponsor.
‘‘Collection of information’’ is defined
in in the PRA and includes agency
requests or requirements that members
of the public submit reports, keep
records, or provide information to a
third party. The PRA requires Federal
agencies to provide a 60-day notice in
the Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information,
before submitting the collection to OMB
for approval. To comply with this
requirement, ACL is publishing a notice
of the proposed collection of
information set forth in this document.
With respect to the following collection
of information, ACL invites comments
on our burden estimates or any other
aspect of this collection of information,
including:
(1) whether the proposed collection of
information is necessary for the proper
performance of ACL’s functions,
PO 00000
Frm 00046
Fmt 4703
Sfmt 4703
including whether the information will
have practical utility;
(2) the accuracy of ACL’s estimate of
the burden of the proposed collection of
information, including the validity of
the methodology and assumptions used
to determine burden estimates;
(3) ways to enhance the quality,
utility, and clarity of the information to
be collected; and
(4) ways to minimize the burden of
the collection of information on
respondents, including through the use
of automated collection techniques
when appropriate, and other forms of
information technology.
The Administration for Community
Living (ACL) is currently engaged in an
effort to streamline and standardize
grantee profiles across three programs
managed by the Office of Healthcare
Information and Counseling (OHIC): the
State Health Insurance Assistance
Program (SHIP), Senior Medicare Patrol
(SMP), and Medicare Improvements for
Patients and Providers Act (MIPPA).
Grantees in each program must adhere
to a specific set of reporting
requirements and associated reporting
schedules outlined in their Program
Reporting Guidelines. While reporting
requirements are effective in ensuring
grantees data, there is no consistency or
uniformity in how individual grantees
submit their data. For example, SHIP
profiles currently exist; these profiles
are accessible to the SHIP grantee
network via the program’s technical
assistance center, and they can be
updated directly by grantee states. SMP
and MIPPA profiles have yet to be
developed. The goal of this data
collection effort is to obtain consistent
data elements for the three programs
that will allow ACL to reimagine the
E:\FR\FM\27OCN1.SGM
27OCN1
65069
Federal Register / Vol. 87, No. 207 / Thursday, October 27, 2022 / Notices
existing profiles into a comparable set of
data elements across programs.
These data will allow RTI
International, a contractor to ACL, to
develop an updated set of grantee
profiles that are accessible, visually
appealing, and consistent across
programs. Specifically, the purpose of
this data collection effort is to update
the SHIP grantee profiles, which were
last updated in 2016, and develop
similar profiles for SMP and MIPPA.
These profiles will be internal to ACL
and will only be shared with grantees.
A web-based questionnaire will be
emailed to all 125 grant managers
(representing 54 states and territories)
electronically via Smartsheet. The
collected data will be imported into a
dataset and will be used to create
program profiles accessible to ACL and
grantees.
The proposed data collection tools
may be found on the ACL website for
review at: https://www.acl.gov/aboutacl/public-input.
Estimated Program Burden
ACL estimates the burden of this
collection of information as follows:
A maximum of 125 grantees are
expected to respond to the web-based
data collection instrument. The
approximate burden for pre-data
collection preparation is 30 minutes per
respondent and approximate burden for
form completion is 20 minutes per
respondent for a total annual estimate of
103.75 hours. The estimated completion
burden includes time to review the
instructions, read the questions and
complete and responses.
IC BURDEN CHART
Number of
respondents
Respondent/data collection activity
Hours per
response
Annual
burden hours
Pre-data collection preparation ......................................................................
Web-based data collection ............................................................................
125
125
1
1
0.5
0.33
62.5
41.25
Total ........................................................................................................
125
1
0.83
103.75
Dated: October 21, 2022.
Alison Barkoff,
Acting Administrator and Assistant Secretary
for Aging.
[FR Doc. 2022–23364 Filed 10–26–22; 8:45 am]
BILLING CODE 4154–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2022–N–2588]
Quantitative Brain Amyloid Positron
Emission Tomography Imaging in
Patients With Alzheimer’s Disease;
Public Workshop; Request for
Comments
AGENCY:
Food and Drug Administration,
HHS.
Notice of public workshop;
request for comments.
ACTION:
The Food and Drug
Administration (FDA, the Agency, or
we) is announcing the following public
workshop entitled ‘‘Quantitative Brain
Amyloid PET Imaging in Patients with
Alzheimer’s Disease.’’ The purpose of
the public workshop is to evaluate the
role of quantitative positron emission
tomography (PET) measures of amyloid
deposition in the brain in clinical trials
and clinical use in patients with
suspected or confirmed Alzheimer’s
disease.
DATES: The public workshop will be
held on November 17, 2022, from 8:30
a.m. to 5 p.m. Eastern Time. Submit
either electronic or written comments
SUMMARY:
khammond on DSKJM1Z7X2PROD with NOTICES
Responses per
respondent
VerDate Sep<11>2014
16:55 Oct 26, 2022
Jkt 259001
on this public workshop by December
19, 2022. See the SUPPLEMENTARY
INFORMATION section for registration date
and information.
ADDRESSES: The public workshop will
be held at FDA White Oak Campus
Great Room. Entrance for the public
workshop participants (non-FDA
employees) is through Building 1 where
routine security check procedures will
be performed. For parking and security
information, please refer to https://
www.fda.gov/about-fda/visitorinformation.
You may submit comments as
follows. Please note that late, untimely
filed comments will not be considered.
Electronic comments must be submitted
on or before December 19, 2022. The
https://www.regulations.gov electronic
filing system will accept comments
until 11:59 p.m. Eastern Time at the end
of December 19, 2022. Comments
received by mail/hand delivery/courier
(for written/paper submissions) will be
considered timely if they are
postmarked or the delivery service
acceptance receipt is on or before that
date.
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal:
https://www.regulations.gov. Follow the
instructions for submitting comments.
Comments submitted electronically,
including attachments, to https://
www.regulations.gov will be posted to
the docket unchanged. Because your
comment will be made public, you are
solely responsible for ensuring that your
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comment does not include any
confidential information that you or a
third party may not wish to be posted,
such as medical information, your or
anyone else’s Social Security number, or
confidential business information, such
as a manufacturing process. Please note
that if you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be
posted on https://www.regulations.gov.
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand Delivery/Courier (for
written/paper submissions): Dockets
Management Staff (HFA–305), Food and
Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Dockets Management
Staff, FDA will post your comment, as
well as any attachments, except for
information submitted, marked and
identified, as confidential, if submitted
as detailed in ‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2022–N–2588 for ‘‘Quantitative Brain
Amyloid PET Imaging in Patients with
Alzheimer’s Disease.’’ Received
comments, those filed in a timely
manner (see ADDRESSES), will be placed
E:\FR\FM\27OCN1.SGM
27OCN1
]]>Agencies
[Federal Register Volume 87, Number 207 (Thursday, October 27, 2022)]
[Notices]
[Pages 65068-65069]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-23364]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Community Living
Agency Information Collection Activities: Proposed Collection;
Public Comment Request; of the Office of Healthcare Information and
Counseling (OHIC) Profiles at ACL OMB #0985-New
AGENCY: Administration for Community Living, Department of Health and
Human Services.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Administration for Community Living (ACL) is announcing an
opportunity for the public to comment on the proposed collection of
information listed above. Under the Paperwork Reduction Act of 1995
(PRA), Federal agencies are required to publish a notice in the Federal
Register concerning each proposed collection of information, including
each proposed extension of an existing collection of information, and
to allow 60 days for public comment in response to the notice. This is
a new information collection request soliciting comments on the
information collection requirements relating to the Office of
Healthcare Information and Counseling (OHIC) Profiles project at ACL.
DATES: Comments on the collection of information must be submitted
electronically by 11:59 p.m. (EST) or postmarked by December 27, 2022.
ADDRESSES: Submit electronic comments on the collection of information
to: Amanda Cash, [email protected], 202-795-7369. Submit written
comments on the collection of information to Administration for
Community Living, 330 C Street SW, Washington, DC 20201, Attention:
Amanda Cash.
FOR FURTHER INFORMATION CONTACT: Amanda Cash, [email protected],
202-795-7369.
SUPPLEMENTARY INFORMATION: Under the PRA (44 U.S.C. 3501-3520), Federal
agencies must obtain approval from the Office of Management and Budget
(OMB) for each collection of information they conduct or sponsor.
``Collection of information'' is defined in in the PRA and includes
agency requests or requirements that members of the public submit
reports, keep records, or provide information to a third party. The PRA
requires Federal agencies to provide a 60-day notice in the Federal
Register concerning each proposed collection of information, including
each proposed extension of an existing collection of information,
before submitting the collection to OMB for approval. To comply with
this requirement, ACL is publishing a notice of the proposed collection
of information set forth in this document. With respect to the
following collection of information, ACL invites comments on our burden
estimates or any other aspect of this collection of information,
including:
(1) whether the proposed collection of information is necessary for
the proper performance of ACL's functions, including whether the
information will have practical utility;
(2) the accuracy of ACL's estimate of the burden of the proposed
collection of information, including the validity of the methodology
and assumptions used to determine burden estimates;
(3) ways to enhance the quality, utility, and clarity of the
information to be collected; and
(4) ways to minimize the burden of the collection of information on
respondents, including through the use of automated collection
techniques when appropriate, and other forms of information technology.
The Administration for Community Living (ACL) is currently engaged
in an effort to streamline and standardize grantee profiles across
three programs managed by the Office of Healthcare Information and
Counseling (OHIC): the State Health Insurance Assistance Program
(SHIP), Senior Medicare Patrol (SMP), and Medicare Improvements for
Patients and Providers Act (MIPPA). Grantees in each program must
adhere to a specific set of reporting requirements and associated
reporting schedules outlined in their Program Reporting Guidelines.
While reporting requirements are effective in ensuring grantees data,
there is no consistency or uniformity in how individual grantees submit
their data. For example, SHIP profiles currently exist; these profiles
are accessible to the SHIP grantee network via the program's technical
assistance center, and they can be updated directly by grantee states.
SMP and MIPPA profiles have yet to be developed. The goal of this data
collection effort is to obtain consistent data elements for the three
programs that will allow ACL to reimagine the
[[Page 65069]]
existing profiles into a comparable set of data elements across
programs.
These data will allow RTI International, a contractor to ACL, to
develop an updated set of grantee profiles that are accessible,
visually appealing, and consistent across programs. Specifically, the
purpose of this data collection effort is to update the SHIP grantee
profiles, which were last updated in 2016, and develop similar profiles
for SMP and MIPPA. These profiles will be internal to ACL and will only
be shared with grantees.
A web-based questionnaire will be emailed to all 125 grant managers
(representing 54 states and territories) electronically via Smartsheet.
The collected data will be imported into a dataset and will be used to
create program profiles accessible to ACL and grantees.
The proposed data collection tools may be found on the ACL website
for review at: https://www.acl.gov/about-acl/public-input.
Estimated Program Burden
ACL estimates the burden of this collection of information as
follows:
A maximum of 125 grantees are expected to respond to the web-based
data collection instrument. The approximate burden for pre-data
collection preparation is 30 minutes per respondent and approximate
burden for form completion is 20 minutes per respondent for a total
annual estimate of 103.75 hours. The estimated completion burden
includes time to review the instructions, read the questions and
complete and responses.
IC Burden Chart
----------------------------------------------------------------------------------------------------------------
Number of Responses per Hours per Annual burden
Respondent/data collection activity respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Pre-data collection preparation................ 125 1 0.5 62.5
Web-based data collection...................... 125 1 0.33 41.25
----------------------------------------------------------------
Total...................................... 125 1 0.83 103.75
----------------------------------------------------------------------------------------------------------------
Dated: October 21, 2022.
Alison Barkoff,
Acting Administrator and Assistant Secretary for Aging.
[FR Doc. 2022-23364 Filed 10-26-22; 8:45 am]
BILLING CODE 4154-01-P
