Agency Information Collection Activities: Proposed Collection: Public Comment Request; Information Collection Request Title: Ryan White HIV/AIDS Program Client-Level Data Reporting System, OMB No. 0906-0039-Extension, 44376-44377 [2021-17206]
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44376
Federal Register / Vol. 86, No. 153 / Thursday, August 12, 2021 / Notices
Copies of the proposed
collection of information can be
obtained and comments may be
forwarded by emailing
infocollection@acf.hhs.gov.
Alternatively, copies can also be
obtained by writing to the
Administration for Children and
Families, Office of Planning, Research,
and Evaluation (OPRE), 330 C Street,
SW, Washington, DC 20201, Attn: ACF
Reports Clearance Officer. All requests,
emailed or written, should be identified
by the title of the information collection.
SUPPLEMENTARY INFORMATION:
Description: The National Center on
Health, Behavioral Health, and Safety,
in partnership with Child Trends and
the Center for Childhood Resilience at
the Anne & Robert H. Lurie Children’s
Hospital of Chicago (Lurie), will
conduct information collection
activities across 10 sites within Head
Start Region V as part of a small
randomized controlled trial of the Ready
to Learn through Relationships (RLR)
program, a trauma-informed Framework
and Toolkit designed to promote
resilience in young children. In this
evaluation, sites will be matched on a
number of factors that may be related to
ADDRESSES:
implementation and randomized to
either a low- or high-intensity TTA
condition. The low-intensity condition
will receive 4 hours of training, a
‘‘toolkit’’ of activity-based handouts,
and access to virtual TA office hours.
The high-intensity condition will
include 4 hours of additional training
on use of the toolkit modules, 6 hours
of implementation support, and
monthly classroom coaching.
Region V Head Start programs that
choose to voluntarily participate in the
RLR program will be asked to complete
a number of implementation and
outcomes measures and participate in
other evaluation activities. Data
collection will involve virtual semistructured interviews and focus groups
at the end of the evaluation period, webbased surveys (pre and post), a monthly
web-based log of coaching activities
completed, and repeated teacher reports
of practices throughout the day on a
mobile app during 5 weeks across the
school year.
The information to be collected
focuses on teacher practices for
supporting children’s social-emotional
development and on training and
implementation factors that may
enhance these practices, which is
directly relevant to Head Start’s
mission. Information obtained will be
shared with Regional TTA providers
and site administrators to inform their
ongoing and future TTA work. More
specifically, results of the evaluation
will identify the extent to which more
intensive TTA with ongoing coaching
and on-site expert consultation
enhances teacher practice beyond a
lower-intensity TTA approach.
Additionally, data are expected to
identify implementation factors that
may enhance outcomes at both the level
of the teacher and Head Start Centers.
Respondents: All early childhood
centers in Head Start Region V that meet
inclusion criteria will be invited to
submit application forms to participate
in the evaluation, and approximately 10
centers will be selected. Within each
center (or site), we anticipate there will
be three classrooms of 3–5 year olds.
Participants at each center will consist
of 7 or 8 individuals (e.g., directors,
mental health and behavior consultants,
lead and assistant teachers, and
coaches), for a total of 75 individuals
across all centers or sites.
ANNUAL BURDEN ESTIMATES
Instrument
Total number
of respondents
Total number
of responses
per respondent
75
2
0.17
26
75
20
10
50
20
20
20
30
30
30
15
2
1
1
1
14
1
1
2
100
1
1
0.25
1
1
0.10
0.25
0.25
1
0.10
0.07
0.25
1
38
20
10
5
70
5
20
6
210
8
15
lotter on DSK11XQN23PROD with NOTICES1
Trauma-Informed System Change Instrument (TISCI) Questionnaire (all
site staff) .....................................................................................................
Attitudes Related to Trauma-Informed Care (ARTIC) Questionnaire (all site
staff) ...........................................................................................................
Site Application Form (site administrators) ....................................................
Site Administrator Interview ...........................................................................
Coach/Teacher Background Form ................................................................
Coaching Logs ...............................................................................................
Coach Satisfaction Survey ............................................................................
Coach Interview .............................................................................................
Professional Self-Care Scale (PSCS)—teachers ..........................................
Ecological Momentary Assessment (EMA) Survey -teachers .......................
Teacher Satisfaction Survey ..........................................................................
Teacher Focus Group ....................................................................................
Estimated Total Annual Burden
Hours: 433.
Comments: The Department
specifically requests comments 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) 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
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20:11 Aug 11, 2021
Jkt 253001
use of automated collection techniques
or other forms of information
technology. Consideration will be given
to comments and suggestions submitted
within 60 days of this publication.
Authority: Head Start Act Sec. 648.
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2021–17242 Filed 8–11–21; 8:45 am]
BILLING CODE 4184–40–P
PO 00000
Average
burden hours
per response
Total/annual
burden hours
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Health Resources and Services
Administration
Agency Information Collection
Activities: Proposed Collection: Public
Comment Request; Information
Collection Request Title: Ryan White
HIV/AIDS Program Client-Level Data
Reporting System, OMB No. 0906–
0039—Extension
Health Resources and Services
Administration (HRSA), Department of
Health and Human Services.
AGENCY:
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44377
Federal Register / Vol. 86, No. 153 / Thursday, August 12, 2021 / Notices
ACTION:
Notice.
In compliance with the
requirement for opportunity for public
comment on proposed data collection
projects of the Paperwork Reduction Act
of 1995, HRSA announces plans to
submit an Information Collection
Request (ICR), described below, to the
Office of Management and Budget
(OMB). Prior to submitting the ICR to
OMB, HRSA seeks comments from the
public regarding the burden estimate,
below, or any other aspect of the ICR.
DATES: Comments on this ICR should be
received no later than October 12, 2021.
ADDRESSES: Submit your comments to
paperwork@hrsa.gov or by mail to the
HRSA Information Collection Clearance
Officer, Room 14N136B, 5600 Fishers
Lane, Rockville, MD 20857.
FOR FURTHER INFORMATION CONTACT: 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 Lisa Wright-Solomon, the HRSA
Information Collection Clearance Officer
at (301) 443–1984.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the
information collection request title for
reference, pursuant to Section
3506(c)(2)(A), the Paperwork Reduction
Act of 1995.
Information Collection Request Title:
Ryan White HIV/AIDS Program ClientSUMMARY:
Level Data Reporting System: OMB No.
0906–0039—Extension.
Abstract: The Ryan White HIV/AIDS
Program (RWHAP), authorized under
Title XXVI of the Public Health Service
Act, is administered by HRSA’s HIV/
AIDS Bureau. HRSA awards funding to
recipients in areas of the greatest need
to respond effectively to the changing
HIV epidemic, with an emphasis on
providing life-saving and life-extending
medical care, treatment, and support
services for people living with HIV in
the United States.
RWHAP reporting requirements
include the annual submission of clientlevel data in the RWHAP Services
Report (RSR). RSR collects information
from grant recipients and their
subcontracted service providers, funded
under Parts A, B, C, and D of the
RWHAP legislation. HRSA is requesting
an extension of the current RSR with no
changes.
Need and Proposed Use of the
Information: RWHAP legislation
specifies HRSA’s responsibilities in
administering grant funds, allocating
funding, assessing HIV care outcomes
(e.g., viral suppression), and serving
particular populations. RSR collects
data on the characteristics of RWHAPfunded recipients, their contracted
service providers, and the patients or
clients served. RSR system consists of
two primary components, the Recipient
Report and the Provider Report, and a
data file containing the client-level data
elements. Data is submitted annually.
RWHAP legislation specifies the
importance of recipient accountability
and linking performance to budget. RSR
is used to ensure recipient compliance
with the law, including evaluating the
effectiveness of programs, monitoring
recipient and provider performance, and
informing annual reports to Congress.
Information collected through the RSR
is critical for HRSA, state and local
grant recipients, and individual
providers to assess the status of existing
HIV-related service delivery systems,
assess trends in service utilization,
assess the impact of data reporting and
identify areas of greatest need.
Likely Respondents: RWHAP grant
recipients, as well as their
subcontracted service providers, funded
under RWHAP parts A, B, C, and D.
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
lotter on DSK11XQN23PROD with NOTICES1
Form name
Number of
responses
per respondent
Total
responses
Average
burden
per
response
(in hours)
Total
burden hours
Recipient Report ..................................................................
Provider Report ....................................................................
Client Report ........................................................................
595
2,063
1,532
1
1
1
595
2,063
1,532
11
13
113
6,545
26,819
173,116
Total ..............................................................................
4,190
........................
4,190
........................
206,480
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
20:59 Aug 11, 2021
Jkt 253001
technology to minimize the information
collection burden.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Maria G. Button,
Director, Executive Secretariat.
Office of the Secretary
[FR Doc. 2021–17206 Filed 8–11–21; 8:45 am]
PO 00000
Frm 00046
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Delegation of Authority
Notice is hereby given that I have
delegated to the Administrator, Health
Resources and Services Administration
(HRSA), or their successor, the
authorities that are vested in the
Secretary of Health and Human Services
under section 1150C of the Social
Security Act (42 U.S.C. 1301 et seq.), as
added by section 9911 of the American
BILLING CODE 4165–15–P
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]]>Agencies
[Federal Register Volume 86, Number 153 (Thursday, August 12, 2021)]
[Notices]
[Pages 44376-44377]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-17206]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Health Resources and Services Administration
Agency Information Collection Activities: Proposed Collection:
Public Comment Request; Information Collection Request Title: Ryan
White HIV/AIDS Program Client-Level Data Reporting System, OMB No.
0906-0039--Extension
AGENCY: Health Resources and Services Administration (HRSA), Department
of Health and Human Services.
[[Page 44377]]
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with the requirement for opportunity for public
comment on proposed data collection projects of the Paperwork Reduction
Act of 1995, HRSA announces plans to submit an Information Collection
Request (ICR), described below, to the Office of Management and Budget
(OMB). Prior to submitting the ICR to OMB, HRSA seeks comments from the
public regarding the burden estimate, below, or any other aspect of the
ICR.
DATES: Comments on this ICR should be received no later than October
12, 2021.
ADDRESSES: Submit your comments to [email protected] or by mail to the
HRSA Information Collection Clearance Officer, Room 14N136B, 5600
Fishers Lane, Rockville, MD 20857.
FOR FURTHER INFORMATION CONTACT: To request more information on the
proposed project or to obtain a copy of the data collection plans and
draft instruments, email [email protected] or call Lisa Wright-
Solomon, the HRSA Information Collection Clearance Officer at (301)
443-1984.
SUPPLEMENTARY INFORMATION: When submitting comments or requesting
information, please include the information collection request title
for reference, pursuant to Section 3506(c)(2)(A), the Paperwork
Reduction Act of 1995.
Information Collection Request Title: Ryan White HIV/AIDS Program
Client-Level Data Reporting System: OMB No. 0906-0039--Extension.
Abstract: The Ryan White HIV/AIDS Program (RWHAP), authorized under
Title XXVI of the Public Health Service Act, is administered by HRSA's
HIV/AIDS Bureau. HRSA awards funding to recipients in areas of the
greatest need to respond effectively to the changing HIV epidemic, with
an emphasis on providing life-saving and life-extending medical care,
treatment, and support services for people living with HIV in the
United States.
RWHAP reporting requirements include the annual submission of
client-level data in the RWHAP Services Report (RSR). RSR collects
information from grant recipients and their subcontracted service
providers, funded under Parts A, B, C, and D of the RWHAP legislation.
HRSA is requesting an extension of the current RSR with no changes.
Need and Proposed Use of the Information: RWHAP legislation
specifies HRSA's responsibilities in administering grant funds,
allocating funding, assessing HIV care outcomes (e.g., viral
suppression), and serving particular populations. RSR collects data on
the characteristics of RWHAP-funded recipients, their contracted
service providers, and the patients or clients served. RSR system
consists of two primary components, the Recipient Report and the
Provider Report, and a data file containing the client-level data
elements. Data is submitted annually. RWHAP legislation specifies the
importance of recipient accountability and linking performance to
budget. RSR is used to ensure recipient compliance with the law,
including evaluating the effectiveness of programs, monitoring
recipient and provider performance, and informing annual reports to
Congress. Information collected through the RSR is critical for HRSA,
state and local grant recipients, and individual providers to assess
the status of existing HIV-related service delivery systems, assess
trends in service utilization, assess the impact of data reporting and
identify areas of greatest need.
Likely Respondents: RWHAP grant recipients, as well as their
subcontracted service providers, funded under RWHAP parts A, B, C, and
D.
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 Average burden
Form name Number of responses per Total per response Total burden
respondents respondent responses (in hours) hours
----------------------------------------------------------------------------------------------------------------
Recipient Report................ 595 1 595 11 6,545
Provider Report................. 2,063 1 2,063 13 26,819
Client Report................... 1,532 1 1,532 113 173,116
-------------------------------------------------------------------------------
Total....................... 4,190 .............. 4,190 .............. 206,480
----------------------------------------------------------------------------------------------------------------
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 technology to
minimize the information collection burden.
Maria G. Button,
Director, Executive Secretariat.
[FR Doc. 2021-17206 Filed 8-11-21; 8:45 am]
BILLING CODE 4165-15-P
