Advisory Council on Alzheimer's Research, Care, and Services; Meeting, 46801-46802 [2023-15406]
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46801
Federal Register / Vol. 88, No. 138 / Thursday, July 20, 2023 / Notices
To
request more information on the
proposed project or to obtain a copy of
the data collection plans and draft
instruments, email paperwork@hrsa.gov
or call Samantha Miller, the HRSA
Information Collection Clearance
Officer, at (301) 443–3983.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the ICR title
for reference.
Information Collection Request Title:
Rural Health Network Development
Program Performance Improvement
Measurement System, OMB No. 0906–
0010—Revision.
Abstract: The Rural Health Network
Development (RHND) program is
authorized under section 330A(f) of the
Public Health Service Act (42 U.S.C.
254c(f)). The purpose of this program is
to support integrated health care
networks that collaborate to achieve
efficiencies; expand access to,
coordinate, and improve the quality of
basic health care services and associated
health outcomes; and strengthen the
rural health care system as a whole. The
program supports networks as they
address gaps in service, enhance
systems of care, and expand capacity of
the local health care system.
RHND-funded programs promote
population health management and the
transition towards value-based care
through diverse network participants
that includes traditional and nontraditional network partners. Evidence
of program impact demonstrated by
outcome data and program
sustainability are integral components
FOR FURTHER INFORMATION CONTACT:
of the program. This is a 4-year
competitive program for networks
composed of at least three participants
that are existing health care providers.
At least 66 percent of network
participants must be located in a HRSAdesignated rural area.
HRSA currently collects information
about RHND awards using an OMBapproved set of performance measures
and seeks to revise that approved
collection. The proposed revisions are
being implemented to better gather
award recipient data in response to
previously accumulated award recipient
feedback, peer-reviewed research, and
information gathered from the
previously approved RHND measures.
Need and Proposed Use of the
Information: This program needs
measures that will enable HRSA to
provide aggregate program data required
by Congress under the Government
Performance and Results Act of 1993.
These measures cover the principal
topic areas of interest to HRSA,
including (a) access to care, (b)
population demographics, (c) staffing,
(d) consortium/network, (e)
sustainability, and (f) project specific
domains. All measures will evaluate
HRSA’s progress toward achieving its
goals.
The proposed changes include
additional components under questions
surrounding the network’s benefits and
funding strategies, as well as the types
of participant organizations. Questions
surrounding Health Information
Technology and Telehealth have been
modified to reflect an updated
telehealth definition based on renewed
knowledge on the use of both Health
Information Technology and Telehealth,
and to improve understanding of how
these important technologies are
affecting HRSA award recipients. The
Demographics and Services section now
includes a question requesting grantees
to identify which counties they have
served during the project. Finally,
revised National Quality Forum and
Centers for Medicare & Medicaid
Services measures were included to
allow uniform collection efforts
throughout the HRSA Federal Office of
Rural Health Policy. The total number of
responses has remained at 44 since the
previous ICR. The new RHND grant
cycle maintained the same number of
award recipients and number of
respondents.
Likely Respondents: Respondents will
be award recipients of the Rural Health
Network Development Program.
Burden Statement: Burden in this
context means the time expended by
persons to generate, maintain, retain,
disclose, or provide the information
requested. This includes the time
needed to review instructions; to
develop, acquire, install, and utilize
technology and systems for the purpose
of collecting, validating, and verifying
information, processing and
maintaining information, and disclosing
and providing information; to train
personnel and to be able to respond to
a collection of information; to search
data sources; to complete and review
the collection of information; and to
transmit or otherwise disclose the
information. The total annual burden
hours estimated for this ICR are
summarized in the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
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Form name
Number of
responses per
respondent
Total
responses
Average
burden per
response
(in hours)
Total burden
hours
Performance Improvement and Measurement System
Database ..........................................................................
44
1
44
6
264
Total ..............................................................................
44
1
44
6
264
HRSA specifically requests comments
on (1) the necessity and utility of the
proposed information collection for the
proper performance of the agency’s
functions; (2) the accuracy of the
estimated burden; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4) the
use of automated collection techniques
or other forms of information
VerDate Sep<11>2014
17:19 Jul 19, 2023
Jkt 259001
technology to minimize the information
collection burden.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Maria G. Button,
Director, Executive Secretariat.
Advisory Council on Alzheimer’s
Research, Care, and Services; Meeting
[FR Doc. 2023–15400 Filed 7–19–23; 8:45 am]
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Assistant Secretary for
Planning and Evaluation, HHS.
AGENCY:
ACTION:
Notice of meeting.
This notice announces the
public meeting of the Advisory Council
on Alzheimer’s Research, Care, and
SUMMARY:
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46802
Federal Register / Vol. 88, No. 138 / Thursday, July 20, 2023 / Notices
Services (Advisory Council). The
Advisory Council provides advice on
how to prevent or reduce the burden of
Alzheimer’s disease and related
dementias (ADRD) on people with the
disease and their caregivers. During the
meeting on July 31, 2023, the Advisory
Council subcommittees will present
their recommendations for adoption by
the full Advisory Council. The meeting
will also include a presentation on the
Alzheimer’s disease bypass budget from
the National Institutes of Health (NIH),
a National Healthy Brain Initiative Road
Map Series update by the Centers for
Disease Control and Prevention (CDC),
and federal updates.
DATES: The meeting will be held
virtually on July 31, 2023 from 9:30 a.m.
to 4:30 a.m. EST.
ADDRESSES: The meeting will be a
hybrid of in-person and virtual. The
meeting will be held in Room 800 of the
Hubert H. Humphrey Building, 200
Independence Avenue SW, Washington,
DC 20201. It will also stream live at
www.hhs.gov/live.
Comments: Time is allocated on the
agenda to hear public comments from
4:00 p.m. to 4:30 p.m. The time for oral
comments will be limited to two (2)
minutes per individual. In order to
provide a public comment, please
register by emailing your name to
napa@hhs.gov by Thursday, July 27.
Registered commenters will receive both
a dial-in number and a link to join the
meeting virtually; individuals will have
the choice to either join virtually via the
link, or to call in only by using the dialin number. Note: There may be a 30–45
second delay in the livestream video
presentation of the conference. For this
reason, if you have pre-registered to
submit a public comment, it is
important to connect to the meeting by
3:45 p.m. to ensure that you do not miss
your name and allotted time when
called. If you miss your name and
allotted time to speak, you may not be
able to make your public comment.
Public commenters will not be admitted
to the virtual meeting before 3:30 p.m.
but are encouraged to watch the meeting
at www.hhs.gov/live. Should you have
questions during the session, please
email napa@hhs.gov and someone will
respond to your message as quickly as
possible.
In order to ensure accuracy, please
submit a written copy of oral comments
for the record by emailing napa@
hhs.gov by Tuesday, August 1, 2023.
These comments will be shared on the
website and reflected in the meeting
minutes.
In lieu of oral comments, formal
written comments may be submitted for
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17:49 Jul 19, 2023
Jkt 259001
the record by Tuesday, August 1, 2023
to Helen Lamont, Ph.D., OASPE, 200
Independence Avenue SW, Room 424E,
Washington, DC 20201. Comments may
also be sent to napa@hhs.gov. Those
submitting written comments should
identify themselves and any relevant
organizational affiliations.
FOR FURTHER INFORMATION CONTACT:
Helen Lamont, 202–260–6075,
helen.lamont@hhs.gov. Note: The
meeting will be available to the public
live at www.hhs.gov/live.
Notice of
these meetings is given under the
Federal Advisory Committee Act (5
U.S.C. app. 2, section 10(a)(1) and
(a)(2)). Topics of the Meeting:
subcommittee recommendations, NIA
bypass budget, FDA drug coverage
decisions, and CDC Health Brain
Initiative.
Procedure and Agenda: The meeting
will be webcast at www.hhs.gov/live and
video recordings will be added to the
National Alzheimer’s Project Act
website when available after the
meeting. This meeting is open to the
public. Please allow 30 minutes to go
through security and walk to the
meeting room. Participants joining in
person should note that seating may be
limited. Those wishing to attend the
meeting in person must send an email
to napa@hhs.gov and put ‘‘July 31
Meeting Attendance’’ in the subject line
by Thursday, July 27 so that their names
may be put on a list of expected
attendees and forwarded to the security
officers at the Department of Health and
Human Services. Any interested
member of the public who is a non-U.S.
citizen should include this information
at the time of registration to ensure that
the appropriate security procedure to
gain entry to the building is carried out.
Although the meeting is open to the
public, procedures governing security
and the entrance to Federal buildings
may change without notice. If you wish
to make a public comment, you must
note that within your email.
Authority: 42 U.S.C. 11225; section
2(e)(3) of the National Alzheimer’s
Project Act. The panel is governed by
provisions of Public Law 92–463, as
amended (5 U.S.C. appendix 2), which
sets forth standards for the formation
and use of advisory committees.
SUPPLEMENTARY INFORMATION:
Miranda Lynch-Smith,
Senior Official Performing the Duties of the
Assistant Secretary for Planning and
Evaluation Deputy Assistant Secretary for
Human Services Policy.
[FR Doc. 2023–15406 Filed 7–19–23; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Request for Comments on the Draft
HHS Scientific Integrity Policy
Office of the Secretary, Office
of the Assistant Secretary for Planning
and Evaluation, HHS.
ACTION: Notice request for comment
(RFC).
AGENCY:
The Department of Health and
Human Services (HHS) is seeking public
comment on its draft Scientific Integrity
Policy through the Department of Health
and Human Services website at https://
www.hhs.gov/programs/research/
scientificintegrity.
SUMMARY:
Submit comments on or before
September 1, 2023.
ADDRESSES: Written comments can be
provided by email, Fax, or U.S. mail.
Email: scientificintegrity@hhs.gov.
Fax: (202) 690–5882.
Mail: U.S. Department of Health and
Human Services, Office of the Assistant
Secretary for Planning and Evaluation,
Office of Science and Data Policy, Attn:
Scientific Integrity Comments, 200
Independence Avenue SW, Room 429E,
Washington, DC 20201.
FOR FURTHER INFORMATION CONTACT:
Casey Sullivan, (202) 205–8189.
SUPPLEMENTARY INFORMATION: The draft
Department of Health and Human
Services Scientific Integrity Policy is
provided as part of implementation of
the Presidential Memorandum on
Restoring Trust in Government Through
Scientific Integrity and Evidence-based
Policymaking,1 to ensure that Agency
stakeholders are given an opportunity to
comment on this policy.
HHS developed the draft Scientific
Integrity Policy (the draft policy) based
on the National Science and Technology
Council Framework for Federal
Scientific Integrity Policy and Practice.2
The draft policy includes specific
provisions prohibiting political
interference, ensuring independent
review of scientific activities,
facilitating the free flow of scientific
information, prohibiting suppression or
delay of scientific findings for nonscientific reasons, forbidding censorship
or alteration of scientific findings, and
protecting against retaliation. The draft
policy also establishes clear procedures
for reporting and handling allegations of
DATES:
1 https://www.whitehouse.gov/briefing-room/
presidential-actions/2021/01/27/memorandum-onrestoring-trust-in-government-through-scientificintegrity-and-evidence-based-policymaking/.
2 https://www.whitehouse.gov/wp-content/
uploads/2023/01/01-2023-Framework-for-FederalScientific-Integrity-Policy-and-Practice.pdf.
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Agencies
[Federal Register Volume 88, Number 138 (Thursday, July 20, 2023)]
[Notices]
[Pages 46801-46802]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-15406]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Advisory Council on Alzheimer's Research, Care, and Services;
Meeting
AGENCY: Assistant Secretary for Planning and Evaluation, HHS.
ACTION: Notice of meeting.
-----------------------------------------------------------------------
SUMMARY: This notice announces the public meeting of the Advisory
Council on Alzheimer's Research, Care, and
[[Page 46802]]
Services (Advisory Council). The Advisory Council provides advice on
how to prevent or reduce the burden of Alzheimer's disease and related
dementias (ADRD) on people with the disease and their caregivers.
During the meeting on July 31, 2023, the Advisory Council subcommittees
will present their recommendations for adoption by the full Advisory
Council. The meeting will also include a presentation on the
Alzheimer's disease bypass budget from the National Institutes of
Health (NIH), a National Healthy Brain Initiative Road Map Series
update by the Centers for Disease Control and Prevention (CDC), and
federal updates.
DATES: The meeting will be held virtually on July 31, 2023 from 9:30
a.m. to 4:30 a.m. EST.
ADDRESSES: The meeting will be a hybrid of in-person and virtual. The
meeting will be held in Room 800 of the Hubert H. Humphrey Building,
200 Independence Avenue SW, Washington, DC 20201. It will also stream
live at www.hhs.gov/live.
Comments: Time is allocated on the agenda to hear public comments
from 4:00 p.m. to 4:30 p.m. The time for oral comments will be limited
to two (2) minutes per individual. In order to provide a public
comment, please register by emailing your name to [email protected] by
Thursday, July 27. Registered commenters will receive both a dial-in
number and a link to join the meeting virtually; individuals will have
the choice to either join virtually via the link, or to call in only by
using the dial-in number. Note: There may be a 30-45 second delay in
the livestream video presentation of the conference. For this reason,
if you have pre-registered to submit a public comment, it is important
to connect to the meeting by 3:45 p.m. to ensure that you do not miss
your name and allotted time when called. If you miss your name and
allotted time to speak, you may not be able to make your public
comment. Public commenters will not be admitted to the virtual meeting
before 3:30 p.m. but are encouraged to watch the meeting at
www.hhs.gov/live. Should you have questions during the session, please
email [email protected] and someone will respond to your message as quickly
as possible.
In order to ensure accuracy, please submit a written copy of oral
comments for the record by emailing [email protected] by Tuesday, August 1,
2023. These comments will be shared on the website and reflected in the
meeting minutes.
In lieu of oral comments, formal written comments may be submitted
for the record by Tuesday, August 1, 2023 to Helen Lamont, Ph.D.,
OASPE, 200 Independence Avenue SW, Room 424E, Washington, DC 20201.
Comments may also be sent to [email protected]. Those submitting written
comments should identify themselves and any relevant organizational
affiliations.
FOR FURTHER INFORMATION CONTACT: Helen Lamont, 202-260-6075,
[email protected]. Note: The meeting will be available to the public
live at www.hhs.gov/live.
SUPPLEMENTARY INFORMATION: Notice of these meetings is given under the
Federal Advisory Committee Act (5 U.S.C. app. 2, section 10(a)(1) and
(a)(2)). Topics of the Meeting: subcommittee recommendations, NIA
bypass budget, FDA drug coverage decisions, and CDC Health Brain
Initiative.
Procedure and Agenda: The meeting will be webcast at www.hhs.gov/live and video recordings will be added to the National Alzheimer's
Project Act website when available after the meeting. This meeting is
open to the public. Please allow 30 minutes to go through security and
walk to the meeting room. Participants joining in person should note
that seating may be limited. Those wishing to attend the meeting in
person must send an email to [email protected] and put ``July 31 Meeting
Attendance'' in the subject line by Thursday, July 27 so that their
names may be put on a list of expected attendees and forwarded to the
security officers at the Department of Health and Human Services. Any
interested member of the public who is a non-U.S. citizen should
include this information at the time of registration to ensure that the
appropriate security procedure to gain entry to the building is carried
out. Although the meeting is open to the public, procedures governing
security and the entrance to Federal buildings may change without
notice. If you wish to make a public comment, you must note that within
your email.
Authority: 42 U.S.C. 11225; section 2(e)(3) of the National
Alzheimer's Project Act. The panel is governed by provisions of Public
Law 92-463, as amended (5 U.S.C. appendix 2), which sets forth
standards for the formation and use of advisory committees.
Miranda Lynch-Smith,
Senior Official Performing the Duties of the Assistant Secretary for
Planning and Evaluation Deputy Assistant Secretary for Human Services
Policy.
[FR Doc. 2023-15406 Filed 7-19-23; 8:45 am]
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