Agency Information Collection Activities; Submission for OMB Review; Public Comment Request; of the State Councils on Developmental Disabilities, 6742-6744 [2023-02016]
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6742
Federal Register / Vol. 88, No. 21 / Wednesday, February 1, 2023 / Notices
The SHIP vision is to be the known
and trusted community resource for
Medicare information. Four strategic
themes provide support for that vision.
They are: (1) Service Excellence, (2)
Capacity Building, (3) Operational
Excellence, and (4) Innovation. Within
each theme are a series of goals and
objectives that can be used to achieve
the overall vision for the project.
There are currently 54 active SHIP
grants; one in every state, the District of
Columbia, Puerto Rico, Guam, and the
U.S. Virgin Islands. The funds awarded
through this application are for the
Commonwealth of the Northern Mariana
Islands to establish and implement the
SHIP program. The project period will
run April 1, 2023 through March 31,
2025. Eligible applicants include the
State Office of Insurance, the State
Medicaid Office, or the State
Department on Aging as designated by
the Commonwealth of the Northern
Mariana Islands, who demonstrate their
ability and commitment to providing
SHIP services statewide.
II. Award Information
4. Intergovernmental Review:
Executive Order 12372,
Intergovernmental Review of Federal
Programs, is not applicable to these
grant applications.
IV. Submission Information
1. Application Instructions
Application Instructions are available
via email. Contact Margaret Flowers at
Margaret.flowers@acl.hhs.gov.
2. Submission Dates and Times
To receive consideration, applications
must be submitted by 11:59 p.m. Eastern
Time on April 3, 2023 via email to
Margaret Flowers at Margaret.flowers@
acl.hhs.gov.
VII. Agency Contacts
Direct inquiries regarding
programmatic issues to: Margaret
Flowers, Phone: 202.795.7315, Email:
Margaret.Flowers@acl.hhs.gov.
Dated: January 26, 2023.
Alison Barkoff,
Acting Administrator and Assistant Secretary
for Aging.
[FR Doc. 2023–02017 Filed 1–31–23; 8:45 am]
1. Funding Instrument Type
BILLING CODE 4154–01–P
This award will be made in the form
of a cooperative agreement.
lotter on DSK11XQN23PROD with NOTICES1
2. Anticipated Total Funding per Budget
Period
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Funding will be distributed through a
formula as identified in the statute. The
amounts allocated are based upon
factors defined in the statute and will be
distributed based on the formula. ACL
will fund a project period of up to two
(2) years contingent upon the
availability of federal funds. The
applicant for the Commonwealth of the
Northern Mariana Islands is eligible for
$50,000 for the first budget period of
this project.
Administration for Community Living
III. Eligibility Criteria and Other
Requirements
SUMMARY:
1. Eligible Applicants: Eligible
applicants include State Units on Aging
(SUA), State Departments of Insurance
(DOI), or the State Medicaid Agency, as
directed by the state Governor.
2. Cost Sharing or Matching is not
required.
3. Unique Entity ID: All grant
applicants must obtain and keep current
a Unique Entity ID (UEI). On April 4,
2022, the unique entity identifier used
across the federal government changed
from the DUNS Number to the Unique
Entity ID (generated by SAM.gov). The
Unique Entity ID is a 12-character
alphanumeric ID assigned to an entity
by SAM.gov. The UEI is viewable in
your SAM.gov entity registration record.
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Jkt 259001
[OMB Control No. 0985–0033]
Agency Information Collection
Activities; Submission for OMB
Review; Public Comment Request; of
the State Councils on Developmental
Disabilities
Administration for Community
Living, HHS.
ACTION: Notice.
AGENCY:
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 State Councils on
Developmental Disabilities (Councils)
OMB control number 0985–0033.
DATES: Submit written comments on the
collection of information by March 3,
2023.
ADDRESSES: Submit written comments
and recommendations for the proposed
information collection within 30 days of
publication of this notice to
PO 00000
Frm 00047
Fmt 4703
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www.reginfo.gov/public/do/PRAMain.
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: Sara
Newell-Perez, phone: 202–795–7413 or
E-Mail: Sara.Newell-Perez@acl.hhs.gov.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, The
Administration for Community Living
(ACL) has submitted the following
proposed collection of information to
OMB for review and clearance. ACL is
requesting approval to collect data for
the State Councils on Developmental
Disabilities (Councils) OMB control
number 0985–0033.
The State Councils on Developmental
Disabilities (Councils) are authorized by
Subtitle B, of the Developmental
Disabilities Assistance and Bill of Rights
Act of 2000 (DD Act), as amended, [42
U.S.C. 15001 et seq.] (The DD Act). The
DD Act requires them to submit an
annual Program Performance Report.
Section 125(c)(7) 42 U.S.C. 15025 states
that: Beginning in fiscal year 2002, the
Council shall annually prepare and
transmit to the Secretary a report. Each
report shall be in a form prescribed by
the Secretary by regulation under
section 104(b). Each report shall contain
information about the progress made by
the Council in achieving the goals of the
Council as specified in section
124(c)(4)).
This is a revision of a currently
approved information collection. While
the DDC PPR remains the same and is
consistent with performance measures
previously approved in the State Plan
template, the revisions include items for
collecting information from Councils on
their use of CDC funds to expand
vaccine access and Public Health
Workforce funds (PHWF) to strengthen
the public health workforce.
The information collected from the
DD Councils is used for multiple
purposes:
(1) To develop and submit at least
every two years a report to the
President, Congress, and the National
Council on Disability that describes the
goals and outcomes of programs
supported under the DD Act.
(2) As a tool for DD Councils to
measure and report on progress in
reaching goals and identify areas for
which revisions are indicated;
(3) To enhance the Federal project
officers’ monitoring of DD Council
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6743
Federal Register / Vol. 88, No. 21 / Wednesday, February 1, 2023 / Notices
progress in reaching projected
outcomes;
(4) As a set of performance measures
to comply with the GPRA
Modernization Act of 2010 (GPRAMA)
that will yield a national portrait of DD
Council program impact; and
(5) For making funding and
appropriation decisions about the DD
Council program.
This IC revision adds items to ensure
ACL is gathering the necessary and
relevant demographic information in
support of Executive Order on
Advancing Racial Equity and Support
for Underserved Communities Through
the Federal Government and the
Executive Order on Advancing Equality
for Lesbian, Gay, Bisexual, Transgender,
Queer, and Intersex Individuals. The
National Academies of Science,
Engineering, and Medicine (NASEM)
recently published a report on
Measuring Sex, Gender Identity, and
Sexual Orientation for the National
Institutes of Health. This report
represents the culmination of years of
work within HHS to develop sexual
Data collection form
PPR (Commenters 1, 3, 4, 5) ...
Some of the performance measure calculations are too distinct
to accurately collect information from sub-grantees. The performance measures, designed to standardize data collection,
often seem to render it meaningless in that it is difficult to
begin to assess whether another Council’s initiative might be
considered here. The policy environments in which Councils
operate make it unclear whether the data collection has practical utility to the public. At present, there is no public-facing
easily digestible summary of the data for public review. The
current PPR has no practical utility beyond ACL staff.
There should be a different strategy to collect and compile stories from DD Councils that would be more useful to ACL. Including it in PPR narrative reporting does not seem to address ongoing story needs.
The PPR only allows for narrative addressing ICF and HCBS
updates. Councils should be able to import initial Comprehensive Review and Analysis on these issues from the 5-year
state plan and any subsequent update from state plan PPRs
during the five-year reporting cycle.
There is often a wide discrepancy between the number of people with I/DD and their family members who participate in
Council supported activities and the number of people with I/
DD and their family members who respond to a survey impacting the validity of Outcome and Sub-Outcome Measures.
It is difficult to address how to collect data about SOGI without
knowing what the federal data subcommittee is recommending. We also have state Data Privacy Laws that must be
considered once we receive more information about implementation of these Executive Orders. State law may prohibit
collection of certain data.
PPR (Commenter 2) ..................
PPR (Commenter 5) ..................
Estimated Program Burden: Based on
the Council reporting experience,
current data and reporting efforts
constitute approximately 172 burden
hours per grantee for a total of 9,632
annual burden hours. Councils worked
with the technical assistance (TA)
Burden calculation was based on the average data entry estimates shared by a sample size of Councils. While Councils
range in staffing size, number of goals and activities they provide response to in the PPR. Past workgroups comprised of
DD Council staff developed the existing PPR tool after much
consensus building conversations and a thorough vetting
process. ACL will continue to have conversations on areas for
potential streamlining as part of our continuous quality improvement efforts. Areas where the reporting platform can assist in streamlining will be taken under consideration.
ACL continues to work with Councils to not only meet the federal data reporting requirement needs, be informed of program progress, but to also understand Council’s use of the
PPR as they share annual reports with citizens and stakeholders in their state/territory. T/TA guidance on ways to best
collect and utilize performance measures data will be provided.
ACL will explore ways to gather grantee stories that meet the
needs of the agency and outside stakeholders in a real-time,
realistic way that does not increase overall burden.
ACL will explore expanding the narrative space available in the
reporting platform to help Councils and ACL better measure
Council projects and activities that impact systems change efforts across the five-year planning cycle.
Through T/TA efforts, Councils will be provided with additional
strategies for capturing quantitative performance of sub-grantees, particularly in a virtual format, improving overall response
rates of activity participants.
ACL continues to review all Federal requirements for SOGI and
will work to ensure T/TA is provided to clarify expectations
and address concerns.
provider to establish burden reporting
estimates for Centers for Disease Control
(CDC) and Public Health Workforce
(PHWF) reporting for a total of 4,874
hours. It should be noted that not all
Councils chose to accept CDC and
PHWF funds. The total addition of
Number of
respondents
Respondent/data collection activity
lotter on DSK11XQN23PROD with NOTICES1
A notice published in the Federal
Register 87 FR 58356 on September 26,
2022. There were five comments
received during the 60-day FRN. ACL’s
responses to these comments are
included below.
ACL response
Burden hours do not accurately reflect the work of the Council
and should be increased.
PPR (Commenter 2) ..................
Comments in Response to the 60-Day
Federal Register Notice
Comment
PPR (Commenters 1, 3, 4, 5) ...
PPR (Commenter 1) ..................
orientation and gender identity (SOGI)
data collection methodology. This IC
includes the recommended NASEM
SOGI questions in the Council PPR.
burden for the CDC and PHWF reporting
totals 4,874 annual burden hours. The
overall estimated total annual burden
hours factoring in all three reports is:
14,506.
Responses
per
respondent
Hours per
response
Annual
burden hours
PPR ..................................................................................................................
CDC .................................................................................................................
PHWF ..............................................................................................................
56
53
47
1
1
1
172
76
18
9,632
4,028
846
Total ..........................................................................................................
........................
........................
........................
14,506
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01FEN1
6744
Federal Register / Vol. 88, No. 21 / Wednesday, February 1, 2023 / Notices
Dated: January 26, 2023.
Alison Barkoff,
Acting Administrator and Assistant Secretary
for Aging.
[FR Doc. 2023–02016 Filed 1–31–23; 8:45 am]
BILLING CODE 4154–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Community Living
[OMB Control No. 0985–0030]
Agency Information Collection
Activities; Submission for OMB
Review; Public Comment Request; of
the National Network of University
Centers for Excellence in
Developmental Disabilities Education,
Research, and Service
Administration for Community
Living, HHS.
ACTION: Notice.
AGENCY:
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 National Network of
University Centers for Excellence in
Developmental Disabilities Education,
Research, and Service (UCEDDs) OMB
control number 0985–0030.
DATES: Submit written comments on the
collection of information by March 3,
2023.
ADDRESSES: Submit written comments
and recommendations for the proposed
information collection within 30 days of
publication of this notice to
www.reginfo.gov/public/do/PRAMain.
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:
Pamela O’Brien, 202–795–7417 or
pamela.obrien@acl.hhs.gov.
SUPPLEMENTARY INFORMATION: In
compliance with 44 U.S.C. 3507, The
Administration for Community Living
(ACL) has submitted the following
proposed collection of information to
OMB for review and clearance. ACL is
requesting approval of revisions to the
lotter on DSK11XQN23PROD with NOTICES1
SUMMARY:
VerDate Sep<11>2014
21:04 Jan 31, 2023
Jkt 259001
National Network of University Centers
for Excellence in Developmental
Disabilities Education, Research, and
Service OMB control number 0985–
0030. The National Network of
University Centers for Excellence in
Developmental Disabilities Education,
Research, and Service (UCEDDs) is a
discretionary grant program that
supports the operation and
administration of UCEDDs which are
interdisciplinary education, research,
and public service units of universities
or public or not-for-profit entities
associated with universities that engage
in core functions.
This IC revision adds items to ensure
ACL is gathering the necessary and
relevant demographic information in
support of Executive Order on
Advancing Racial Equity and Support
for Underserved Communities Through
the Federal Government and the
Executive Order on Advancing Equality
for Lesbian, Gay, Bisexual, Transgender,
Queer, and Intersex Individuals. The
National Academies of Science,
Engineering, and Medicine (NASEM)
recently published a report on
Measuring Sex, Gender Identity, and
Sexual Orientation for the National
Institutes of Health. This report
represents the culmination of years of
work within HHS to develop sexual
orientation and gender identity (SOGI)
data collection methodology. This IC
includes the recommended NASEM
SOGI questions.
This IC revision also includes data
elements needed to account for the
activities supported by funding from the
Centers for Disease Control and
Prevention (CDC) to support access to
vaccines for people with disabilities as
well as the funds awarded under the
American Rescue Plan to increase the
Public Health Workforce (PHWF). All
other elements of the template remain
consistent with the currently approved
UCEDD annual report.
Section 104(a) (42 U.S.C. 15004) of
the Developmental Disabilities
Assistance and Bill of Rights Act of
2000 (DD Act) directs the Secretary of
Health and Human Services to develop
and implement a system of program
accountability to monitor the grantees
funded under the DD Act of 2000. The
program accountability system must
include UCEDDs authorized under Part
D of the DD Act of 2000. Section 154(e)
(42 U.S.C. 15064) of the DD Act of 2000
includes requirements for a UCEDD
Annual Report. The UCEDD Annual
Report should contain information on
progress made in achieving the
projected goals of the Center for the
previous year, including:
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Fmt 4703
Sfmt 4703
(1) The extent to which the goals were
achieved;
(2) A description of the strategies that
contributed to achieving the goals;
(3) The extent goals were not
achieved, a description of factors that
impeded the achievement; and
(4) An accounting of the manner in
which funds paid to the Center under
this subtitle for a fiscal year were
expended.
In addition, the DD requires
information on proposed revisions to
the goals and a description of successful
efforts to leverage funds, other than
funds made available under the DD Act.
The DD Act also states grantees must
report on:
(1) Consumer satisfaction with the
advocacy, capacity building, and
systemic change activities of the
UCEDD;
(2) The extent to which the UCEDD’s
advocacy, capacity building, and
systemic change activities resulted in
improvements; and
(3) The extent to which collaboration
was achieved in the areas of advocacy,
capacity building, and systemic change.
Currently, UCEDDs engage in four
broad tasks: conducting
interdisciplinary training, promoting
exemplary community service programs
and providing technical assistance at all
levels from local service delivery to
community and state governments,
conducting research, and disseminating
information to the field. There are 67
UCEDDs throughout the United States
with at least one or more in every State
and Territory, as mandated.
The information derived from data
collection activities will be used for
multiple purposes:
(1) As a tool for UCEDD grantees to
measure and report on progress in
reaching goals and identify areas for
which revisions are indicated;
(2) To enhance the Federal project
officers’ monitoring of UCEDD progress
in reaching projected outcomes;
(3) To provide a set of standardized
performance measures that will yield a
national portrait of UCEDD program
impact; and
(4) For making funding and
appropriation decisions about the
UCEDD program.
The information provided in the
Annual Reports from the UCEDDs is
combined with information reported by
the State Developmental Disabilities
Councils and Protection and Advocacy
agencies to develop a biennial report.
The report describes the goals and
outcomes of programs supported under
the DD Act and is submitted to the
President, Congress, and the National
Council on Disability. The
E:\FR\FM\01FEN1.SGM
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]]>Agencies
[Federal Register Volume 88, Number 21 (Wednesday, February 1, 2023)]
[Notices]
[Pages 6742-6744]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2023-02016]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Community Living
[OMB Control No. 0985-0033]
Agency Information Collection Activities; Submission for OMB
Review; Public Comment Request; of the State Councils on Developmental
Disabilities
AGENCY: Administration for Community Living, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
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 State Councils on Developmental Disabilities (Councils) OMB control
number 0985-0033.
DATES: Submit written comments on the collection of information by
March 3, 2023.
ADDRESSES: Submit written comments and recommendations for the proposed
information collection within 30 days of publication of this notice to
www.reginfo.gov/public/do/PRAMain. 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: Sara Newell-Perez, phone: 202-795-7413
or E-Mail: [email protected].
SUPPLEMENTARY INFORMATION: In compliance with 44 U.S.C. 3507, The
Administration for Community Living (ACL) has submitted the following
proposed collection of information to OMB for review and clearance. ACL
is requesting approval to collect data for the State Councils on
Developmental Disabilities (Councils) OMB control number 0985-0033.
The State Councils on Developmental Disabilities (Councils) are
authorized by Subtitle B, of the Developmental Disabilities Assistance
and Bill of Rights Act of 2000 (DD Act), as amended, [42 U.S.C. 15001
et seq.] (The DD Act). The DD Act requires them to submit an annual
Program Performance Report. Section 125(c)(7) 42 U.S.C. 15025 states
that: Beginning in fiscal year 2002, the Council shall annually prepare
and transmit to the Secretary a report. Each report shall be in a form
prescribed by the Secretary by regulation under section 104(b). Each
report shall contain information about the progress made by the Council
in achieving the goals of the Council as specified in section
124(c)(4)).
This is a revision of a currently approved information collection.
While the DDC PPR remains the same and is consistent with performance
measures previously approved in the State Plan template, the revisions
include items for collecting information from Councils on their use of
CDC funds to expand vaccine access and Public Health Workforce funds
(PHWF) to strengthen the public health workforce.
The information collected from the DD Councils is used for multiple
purposes:
(1) To develop and submit at least every two years a report to the
President, Congress, and the National Council on Disability that
describes the goals and outcomes of programs supported under the DD
Act.
(2) As a tool for DD Councils to measure and report on progress in
reaching goals and identify areas for which revisions are indicated;
(3) To enhance the Federal project officers' monitoring of DD
Council
[[Page 6743]]
progress in reaching projected outcomes;
(4) As a set of performance measures to comply with the GPRA
Modernization Act of 2010 (GPRAMA) that will yield a national portrait
of DD Council program impact; and
(5) For making funding and appropriation decisions about the DD
Council program.
This IC revision adds items to ensure ACL is gathering the
necessary and relevant demographic information in support of Executive
Order on Advancing Racial Equity and Support for Underserved
Communities Through the Federal Government and the Executive Order on
Advancing Equality for Lesbian, Gay, Bisexual, Transgender, Queer, and
Intersex Individuals. The National Academies of Science, Engineering,
and Medicine (NASEM) recently published a report on Measuring Sex,
Gender Identity, and Sexual Orientation for the National Institutes of
Health. This report represents the culmination of years of work within
HHS to develop sexual orientation and gender identity (SOGI) data
collection methodology. This IC includes the recommended NASEM SOGI
questions in the Council PPR.
Comments in Response to the 60-Day Federal Register Notice
A notice published in the Federal Register 87 FR 58356 on September
26, 2022. There were five comments received during the 60-day FRN.
ACL's responses to these comments are included below.
----------------------------------------------------------------------------------------------------------------
Data collection form Comment ACL response
----------------------------------------------------------------------------------------------------------------
PPR (Commenters 1, 3, 4, 5).................. Burden hours do not accurately Burden calculation was based on
reflect the work of the Council the average data entry
and should be increased. estimates shared by a sample
size of Councils. While
Councils range in staffing
size, number of goals and
activities they provide
response to in the PPR. Past
workgroups comprised of DD
Council staff developed the
existing PPR tool after much
consensus building
conversations and a thorough
vetting process. ACL will
continue to have conversations
on areas for potential
streamlining as part of our
continuous quality improvement
efforts. Areas where the
reporting platform can assist
in streamlining will be taken
under consideration.
PPR (Commenters 1, 3, 4, 5).................. Some of the performance measure ACL continues to work with
calculations are too distinct Councils to not only meet the
to accurately collect federal data reporting
information from sub-grantees. requirement needs, be informed
The performance measures, of program progress, but to
designed to standardize data also understand Council's use
collection, often seem to of the PPR as they share
render it meaningless in that annual reports with citizens
it is difficult to begin to and stakeholders in their
assess whether another state/territory. T/TA guidance
Council's initiative might be on ways to best collect and
considered here. The policy utilize performance measures
environments in which Councils data will be provided.
operate make it unclear whether
the data collection has
practical utility to the
public. At present, there is no
public-facing easily digestible
summary of the data for public
review. The current PPR has no
practical utility beyond ACL
staff.
PPR (Commenter 1)............................ There should be a different ACL will explore ways to gather
strategy to collect and compile grantee stories that meet the
stories from DD Councils that needs of the agency and
would be more useful to ACL. outside stakeholders in a real-
Including it in PPR narrative time, realistic way that does
reporting does not seem to not increase overall burden.
address ongoing story needs.
PPR (Commenter 2)............................ The PPR only allows for ACL will explore expanding the
narrative addressing ICF and narrative space available in
HCBS updates. Councils should the reporting platform to help
be able to import initial Councils and ACL better
Comprehensive Review and measure Council projects and
Analysis on these issues from activities that impact systems
the 5-year state plan and any change efforts across the five-
subsequent update from state year planning cycle.
plan PPRs during the five-year
reporting cycle.
PPR (Commenter 2)............................ There is often a wide Through T/TA efforts, Councils
discrepancy between the number will be provided with
of people with I/DD and their additional strategies for
family members who participate capturing quantitative
in Council supported activities performance of sub-grantees,
and the number of people with I/ particularly in a virtual
DD and their family members who format, improving overall
respond to a survey impacting response rates of activity
the validity of Outcome and Sub- participants.
Outcome Measures.
PPR (Commenter 5)............................ It is difficult to address how ACL continues to review all
to collect data about SOGI Federal requirements for SOGI
without knowing what the and will work to ensure T/TA
federal data subcommittee is is provided to clarify
recommending. We also have expectations and address
state Data Privacy Laws that concerns.
must be considered once we
receive more information about
implementation of these
Executive Orders. State law may
prohibit collection of certain
data.
----------------------------------------------------------------------------------------------------------------
Estimated Program Burden: Based on the Council reporting
experience, current data and reporting efforts constitute approximately
172 burden hours per grantee for a total of 9,632 annual burden hours.
Councils worked with the technical assistance (TA) provider to
establish burden reporting estimates for Centers for Disease Control
(CDC) and Public Health Workforce (PHWF) reporting for a total of 4,874
hours. It should be noted that not all Councils chose to accept CDC and
PHWF funds. The total addition of burden for the CDC and PHWF reporting
totals 4,874 annual burden hours. The overall estimated total annual
burden hours factoring in all three reports is: 14,506.
----------------------------------------------------------------------------------------------------------------
Number of Responses per Hours per Annual burden
Respondent/data collection activity respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
PPR............................................. 56 1 172 9,632
CDC............................................. 53 1 76 4,028
PHWF............................................ 47 1 18 846
---------------------------------------------------------------
Total....................................... .............. .............. .............. 14,506
----------------------------------------------------------------------------------------------------------------
[[Page 6744]]
Dated: January 26, 2023.
Alison Barkoff,
Acting Administrator and Assistant Secretary for Aging.
[FR Doc. 2023-02016 Filed 1-31-23; 8:45 am]
BILLING CODE 4154-01-P
