Submission for OMB Review; OPRE Data Collection for Supporting Youth To Be Successful in Life (SYSIL) (New Collection), 20166-20167 [2021-07752]

Download as PDF 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 Frm 00053 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 PO 00000 Frm 00054 Fmt 4703 Sfmt 4703 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 16APN1

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[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]


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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