Submission for OMB Review; OPRE Data Collection for Supporting Youth To Be Successful in Life (SYSIL) (New Collection), 20166-20167 [2021-07752]
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20166
Federal Register / Vol. 86, No. 72 / Friday, April 16, 2021 / Notices
are to respond, including through the
use of appropriate automated,
electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submissions
of responses; and
5. Assess information collection costs.
Proposed Project
Evaluation of the Chronic Disease
Self-Management Program in the US
Affiliated Pacific Islands (OMB Control
No. 0920–1265, Exp. 06/30/2021)—
Extension—National Center for Chronic
Disease Prevention and Health
Promotion (NCCDPHP), Centers for
Disease Control and Prevention (CDC).
reported effects of the program on
program participants. Because this is the
first time CDSMP is being implemented
in the USAPI, we do not know if the
intervention, which has proven to
improve health outcomes in many
ethnic groups within the United States,
will lead to improved health outcomes
for these communities.
Collecting this data helps us assess
fidelity to and adaptations to the
intervention and to understand if
CDSMP, an evidence-based
intervention, has the same effect in the
US Affiliated Pacific Islands as it has in
multiple ethnic groups within the
United States. CDC requests OMB
approval for an estimated 95 annual
burden hours. There are no costs to
respondents other than their time.
Background and Brief Description
NCCDPHP is evaluating the
implementation of Stanford University’s
Chronic Disease Self-Management
Program (CDSMP) in the US Affiliated
Pacific Islands (USAPI). These
jurisdictions include American Samoa,
Guam, the Commonwealth of the
Northern Mariana Islands, the Republic
of Palau, the Republic of the Marshall
Islands, and the Federated States of
Micronesia.
The purpose of the evaluation is to
understand how CDSMP is being
implemented in the region, to identify
barriers and facilitators to
implementation, to monitor fidelity to
Stanford University’s model and
document adaptations to the
curriculum, and to understand the self-
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
responses per
respondent
Average
burden per
response
(in hr)
Total burden
(in hr)
Form name
Program Participant ......
Chronic Disease Self-Management Workshop
Evaluation.
Chronic Disease Self-Management Questionnaire (Pre-Post Test).
190
1
10/60
32
190
2
10/60
63
..............................................................................
........................
........................
........................
95
Program Participant ......
Total .......................
Jeffrey M. Zirger,
Lead, Information Collection Review Office,
Office of Scientific Integrity, Office of Science,
Centers for Disease Control and Prevention.
[FR Doc. 2021–07836 Filed 4–15–21; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review; OPRE
Data Collection for Supporting Youth
To Be Successful in Life (SYSIL) (New
Collection)
Office of Planning, Research,
and Evaluation, Administration for
Children and Families, HHS.
ACTION: Request for public comment.
AGENCY:
The Administration for
Children and Families (ACF) is
requesting approval from the Office of
Management and Budget (OMB) for a
new data collection. The Supporting
Youth to be Successful in Life study
(SYSIL) will build evidence on how to
end homelessness among youth and
young adults with experience in the
child welfare system by continuing
work with an organization who
SUMMARY:
jbell on DSKJLSW7X2PROD with NOTICES
Number of
respondents
Type of respondent
VerDate Sep<11>2014
19:57 Apr 15, 2021
Jkt 253001
conducted foundational work as part of
the Youth At-Risk of Homelessness
project (OMB Control Number: 0970–
0445). SYSIL will provide important
information to the field by designing
and conducting a federally led
evaluation of a comprehensive service
model for youth at risk of homelessness.
DATES: Comments due within 30 days of
publication. OMB must make a decision
about the collection of information
between 30 and 60 days after
publication of this document in the
Federal Register. Therefore, a comment
is best assured of having its full effect
if OMB receives it within 30 days of
publication.
ADDRESSES: Written comments and
recommendations for the proposed
information collection should be sent
within 30 days of publication of this
notice to www.reginfo.gov/public/do/
PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function.
SUPPLEMENTARY INFORMATION:
Description: The SYSIL evaluation
includes an implementation study and
an impact study, which will use a
rigorous quasi-experimental design that
includes a comparison group. This new
PO 00000
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Fmt 4703
Sfmt 4703
information collection request includes
the baseline and follow-up survey
instruments for the impact study (a
single instrument administered four
times), and discussion guides for
interviews and focus groups for the
implementation study. The data
collected from the baseline and followup surveys will be used to describe the
characteristics of the study sample of
youth, develop models for estimating
program impacts, and determine
program effectiveness by comparing
outcomes between youth in the
treatment (youth receiving the Pathways
program) and control groups. Data from
the interviews and focus groups will
provide a detailed understanding of
program implementation. We will also
conduct brief check-ins with program
directors using a subset of questions
from the interview guides to collect
information on services provided at two
additional points in time. The study
will also use administrative data from
the child welfare system, homelessness
management information system, and
program providers. Administrative data
will be used in its existing format and
does not impose any new information
collection or recordkeeping
requirements on respondents.
E:\FR\FM\16APN1.SGM
16APN1
20167
Federal Register / Vol. 86, No. 72 / Friday, April 16, 2021 / Notices
Respondents: The baseline and
follow-up surveys will be administered
to youth in the treatment group (youth
receiving the Pathways program) and
youth in the control group who consent
to participate in the study. Interviews
will be conducted with program
leadership and staff. Focus groups will
be conducted with a subset of youth
who are participating in the study.
Check-ins will be conducted with
program directors.
ANNUAL BURDEN ESTIMATES
Instrument
Number of
respondents
(total over
request period)
Number of
responses per
respondent
(total over
request period)
700
630
595
490
30
1
1
1
1
1
.5
.5
.5
.5
1.5
350
315
298
245
45
117
105
99
82
15
6
30
6
2
1
2
.5
1.5
.5
6
45
6
2
15
2
50
50
1
1
1.5
1.5
75
75
25
25
SYSIL Youth Survey—Baseline survey ...........................
SYSIL Youth Survey—Follow-up survey 1 (6 months) ...
SYSIL Youth Survey—Follow-up survey 2 (12 months)
SYSIL Youth Survey—Follow-up survey 3 (24 months)
Interview guide for Pathways sites (treatment sites) .......
Program Director Check-ins for Pathways sites (treatment sites) ....................................................................
Interview guide for comparison sites ...............................
Program Director Check-ins for comparison sites ...........
Focus group discussion guide for Pathways youth
(treatment youth) ..........................................................
Focus group discussion guide for comparison youth ......
Estimated Total Annual Burden
Hours: 487.
Authority: Section 105(b)(5) of the Child
Abuse Prevention and Treatment Act
(CAPTA) of 1978 (42 U.S.C. 5106(b)(5)), as
amended by the CAPTA Reauthorization Act
of 2010 (Pub. L. 111–320).
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2021–07752 Filed 4–15–21; 8:45 am]
BILLING CODE 4184–29–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2021–Z–0025]
Medical Devices; Class I Surgeon’s
and Patient Examination Gloves
Department of Health and
Human Services (HHS), Food and Drug
Administration (FDA).
ACTION: Notice; request for comments.
AGENCY:
The Department of Health and
Human Services (HHS or ‘‘the
Department’’) issued a Notice in the
Federal Register of January 15, 2021,
that, among other things, identified
seven types of reserved class I devices
that the Department had determined no
longer require premarket notification.
The Department and the Food and Drug
Administration (FDA or ‘‘the Agency’’)
have reviewed the prior determination,
including the record supporting it, and
believe that the determination is flawed.
This notice explains the basis for HHS
and FDA’s current view that the seven
types of reserved class I devices
jbell on DSKJLSW7X2PROD with NOTICES
SUMMARY:
VerDate Sep<11>2014
19:57 Apr 15, 2021
Jkt 253001
identified in the January 15, 2021,
Notice require a premarket notification,
and explains why the reasoning
supporting the prior determination was
unsound. HHS and FDA are seeking
comment on the matters discussed in
this notice and will issue a future notice
in the Federal Register containing a
final determination regarding the class I
medical gloves listed in the January 15,
2021, Notice.
DATES: Submit either electronic or
written comments on this Notice by
May 17, 2021.
ADDRESSES: You may submit comments
as follows. Please note that late,
untimely filed comments will not be
considered. Comments must be
submitted by May 17, 2021. The https://
www.regulations.gov electronic filing
system will accept comments until
11:59 p.m. Eastern Time at the end of
May 17, 2021. 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
comment does not include any
confidential information that you or a
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Average
burden per
response
(in hours)
Total burden
(in hours)
Annual burden
(in hours)
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–
2021–Z–0025 for ‘‘Medical Devices;
Class I Reserved Surgeon’s and Patient
Examination Gloves.’’ Received
comments, those filed in a timely
manner (see ADDRESSES), will be placed
in the docket and, except for those
submitted as ‘‘Confidential
Submissions,’’ publicly viewable at
https://www.regulations.gov or at the
E:\FR\FM\16APN1.SGM
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]]>Agencies
[Federal Register Volume 86, Number 72 (Friday, April 16, 2021)]
[Notices]
[Pages 20166-20167]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-07752]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; OPRE Data Collection for Supporting
Youth To Be Successful in Life (SYSIL) (New Collection)
AGENCY: Office of Planning, Research, and Evaluation, Administration
for Children and Families, HHS.
ACTION: Request for public comment.
-----------------------------------------------------------------------
SUMMARY: The Administration for Children and Families (ACF) is
requesting approval from the Office of Management and Budget (OMB) for
a new data collection. The Supporting Youth to be Successful in Life
study (SYSIL) will build evidence on how to end homelessness among
youth and young adults with experience in the child welfare system by
continuing work with an organization who conducted foundational work as
part of the Youth At-Risk of Homelessness project (OMB Control Number:
0970-0445). SYSIL will provide important information to the field by
designing and conducting a federally led evaluation of a comprehensive
service model for youth at risk of homelessness.
DATES: Comments due within 30 days of publication. OMB must make a
decision about the collection of information between 30 and 60 days
after publication of this document in the Federal Register. Therefore,
a comment is best assured of having its full effect if OMB receives it
within 30 days of publication.
ADDRESSES: Written comments and recommendations for the proposed
information collection should be sent within 30 days of publication of
this notice to www.reginfo.gov/public/do/PRAMain. Find this particular
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function.
SUPPLEMENTARY INFORMATION:
Description: The SYSIL evaluation includes an implementation study
and an impact study, which will use a rigorous quasi-experimental
design that includes a comparison group. This new information
collection request includes the baseline and follow-up survey
instruments for the impact study (a single instrument administered four
times), and discussion guides for interviews and focus groups for the
implementation study. The data collected from the baseline and follow-
up surveys will be used to describe the characteristics of the study
sample of youth, develop models for estimating program impacts, and
determine program effectiveness by comparing outcomes between youth in
the treatment (youth receiving the Pathways program) and control
groups. Data from the interviews and focus groups will provide a
detailed understanding of program implementation. We will also conduct
brief check-ins with program directors using a subset of questions from
the interview guides to collect information on services provided at two
additional points in time. The study will also use administrative data
from the child welfare system, homelessness management information
system, and program providers. Administrative data will be used in its
existing format and does not impose any new information collection or
recordkeeping requirements on respondents.
[[Page 20167]]
Respondents: The baseline and follow-up surveys will be
administered to youth in the treatment group (youth receiving the
Pathways program) and youth in the control group who consent to
participate in the study. Interviews will be conducted with program
leadership and staff. Focus groups will be conducted with a subset of
youth who are participating in the study. Check-ins will be conducted
with program directors.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of
Number of responses per Average
Instrument respondents respondent burden per Total burden Annual burden
(total over (total over response (in (in hours) (in hours)
request period) request period) hours)
----------------------------------------------------------------------------------------------------------------
SYSIL Youth Survey--Baseline 700 1 .5 350 117
survey.......................
SYSIL Youth Survey--Follow-up 630 1 .5 315 105
survey 1 (6 months)..........
SYSIL Youth Survey--Follow-up 595 1 .5 298 99
survey 2 (12 months).........
SYSIL Youth Survey--Follow-up 490 1 .5 245 82
survey 3 (24 months).........
Interview guide for Pathways 30 1 1.5 45 15
sites (treatment sites)......
Program Director Check-ins for 6 2 .5 6 2
Pathways sites (treatment
sites).......................
Interview guide for comparison 30 1 1.5 45 15
sites........................
Program Director Check-ins for 6 2 .5 6 2
comparison sites.............
Focus group discussion guide 50 1 1.5 75 25
for Pathways youth (treatment
youth).......................
Focus group discussion guide 50 1 1.5 75 25
for comparison youth.........
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 487.
Authority: Section 105(b)(5) of the Child Abuse Prevention and
Treatment Act (CAPTA) of 1978 (42 U.S.C. 5106(b)(5)), as amended by
the CAPTA Reauthorization Act of 2010 (Pub. L. 111-320).
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2021-07752 Filed 4-15-21; 8:45 am]
BILLING CODE 4184-29-P
