Submission for Office of Management and Budget Review; Behavioral Interventions To Advance Self-Sufficiency-Next Generation (BIAS-NG) (Office of Management and Budget #0970-0502), 66115-66117 [2024-18065]

Download as PDF Federal Register / Vol. 89, No. 157 / Wednesday, August 14, 2024 / Notices persons contact ACAESH@fhfa.gov. Individuals who wish to attend virtually may request a link to the virtual meeting platform. Due to limited seating availability, members of the public who wish to attend are encouraged to consider attending virtually. Attendees who require reasonable accommodation should make their requests by September 6, 2024. Requests received after that date will be considered but may not be possible to accommodate. Additionally, for security reasons, members of the public will be subject to security screening procedures and must present valid photo identification to enter the building. ddrumheller on DSK120RN23PROD with NOTICES1 Notice of Committee Charter Renewal and Objectives and Duties of the Committee Pursuant to the FACA (5 U.S.C. chapter 10), FHFA announces the renewal of the charter of the Committee. The purpose of the Committee is to advise FHFA in the exercise of its oversight functions regarding affordable, equitable, and sustainable housing, including but not limited to, affordable, equitable, and sustainable housing needs, barriers to access, barriers to long-term sustainability, and any regulatory, guidance, or policy changes that may be necessary or beneficial to expand such housing. The Committee will focus on FHFA’s regulated entities—Fannie Mae, Freddie Mac, and the Federal Home Loan Banks—and their respective roles in providing a reliable source of liquidity and funding to support housing finance and community investment in the singlefamily and multifamily housing markets. The duties of the Committee are solely advisory and extend only to its submission of advice and recommendations to FHFA, with supporting information and analysis, which are non-binding on FHFA. No determinations of fact or policy are be made by the Committee. The Committee has no decision-making role, and will have no access to non-public FHFA information, including confidential supervisory or other confidential information. Membership of the Committee The FHFA Director will continue to appoint the members of the Committee as their terms expire. To achieve a fairly balanced membership, FHFA will continue to seek members representative of diverse communities, points of view, institution asset sizes, and geographical locations, with expertise in affordable, sustainable, or equitable housing in single-family and VerDate Sep<11>2014 18:22 Aug 13, 2024 Jkt 262001 multifamily housing. The Committee will include members with expertise, applicable to Fannie Mae, Freddie Mac, or the Federal Home Loan Banks, in the areas related to the duties and authorities of the Committee, such as: (1) fair lending, fair housing, or civil rights; (2) single-family lending, servicing, development, mortgages, or capital markets; (3) multifamily lending, servicing, development, mortgages, capital markets, or investments (i.e. Low-Income Housing Tax Credits); (4) consumer, tenant, or community advocacy; (5) housing market technology; (6) state, local, or tribal government housing policies and programs; and (7) academic or nonacademic affiliated housing research. The Committee consists of approximately 20 members, serving two-year terms. Members serve at the sole discretion of the Director. The Committee will meet regularly, as required to carry out its functions. It is estimated that the Committee will meet at least twice per year. Generally, Committee meetings will be open to the public. Sandra L. Thompson, Director, Federal Housing Finance Agency. [FR Doc. 2024–18116 Filed 8–13–24; 8:45 am] BILLING CODE 8070–01–P FEDERAL RESERVE SYSTEM Change in Bank Control Notices; Acquisitions of Shares of a Bank or Bank Holding Company The notificants listed below have applied under the Change in Bank Control Act (Act) (12 U.S.C. 1817(j)) and § 225.41 of the Board’s Regulation Y (12 CFR 225.41) to acquire shares of a bank or bank holding company. The factors that are considered in acting on the applications are set forth in paragraph 7 of the Act (12 U.S.C. 1817(j)(7)). The public portions of the applications listed below, as well as other related filings required by the Board, if any, are available for immediate inspection at the Federal Reserve Bank(s) indicated below and at the offices of the Board of Governors. This information may also be obtained on an expedited basis, upon request, by contacting the appropriate Federal Reserve Bank and from the Board’s Freedom of Information Office at https://www.federalreserve.gov/foia/ request.htm. Interested persons may express their views in writing on the standards enumerated in paragraph 7 of the Act. PO 00000 Frm 00086 Fmt 4703 Sfmt 4703 66115 Comments received are subject to public disclosure. In general, comments received will be made available without change and will not be modified to remove personal or business information including confidential, contact, or other identifying information. Comments should not include any information such as confidential information that would not be appropriate for public disclosure. Comments regarding each of these applications must be received at the Reserve Bank indicated or the offices of the Board of Governors, Ann E. Misback, Secretary of the Board, 20th Street and Constitution Avenue NW, Washington DC 20551–0001, not later than August 29, 2024. A. Federal Reserve Bank of St. Louis (Holly A. Rieser, Senior Manager) P.O. Box 442, St. Louis, Missouri 63166– 2034. Comments can also be sent electronically to Comments.applications@stls.frb.org: 1. Suzanne L. Shaw, Greensburg, Pennsylvania; to join the Croftcheck Family Control Group, a group acting in concert, to acquire voting shares of Townsend Financial Corporation, and thereby indirectly acquire voting shares of Farmers Bank, both of Parsons, Tennessee. Board of Governors of the Federal Reserve System. Michele Taylor Fennell, Deputy Associate Secretary of the Board. [FR Doc. 2024–18139 Filed 8–13–24; 8:45 am] BILLING CODE P DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Submission for Office of Management and Budget Review; Behavioral Interventions To Advance SelfSufficiency-Next Generation (BIAS– NG) (Office of Management and Budget #0970–0502) Office of Planning, Research, and Evaluation, Administration for Children and Families, U.S. Department of Health and Human Services. ACTION: Request for public comments. AGENCY: The Office of Planning, Research, and Evaluation (OPRE) in the Administration for Children and Families (ACF), U.S. Department of Health and Human Services (HHS) requests Office of Management and Budget (OMB) approval to modify and extend the approval of the ACF Behavioral Interventions to Advance SUMMARY: E:\FR\FM\14AUN1.SGM 14AUN1 66116 Federal Register / Vol. 89, No. 157 / Wednesday, August 14, 2024 / Notices Self-Sufficiency-Next Generation (BIAS–NG) Project Overarching Generic (OMB #: 0970–0502; Expiration date: 8/31/2025.) Under this overarching clearance, ACF collects data as part of rapid cycle testing and evaluation, to inform the design of interventions informed by behavioral science and to better understand the mechanisms and effects of such interventions. Interventions have been and will continue to be developed in the program area domains of Temporary Assistance for Needy Families (TANF), child welfare, and Early Head Start/Head Start (EHS/HS). This revision would also allow for collection of data in the child care program area, and would extend the approval of the overarching generic. These interventions are intended to improve outcomes for participants in these programs. 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. You can also obtain copies of the proposed collection of information by emailing OPREinfocollection@acf.hhs.gov. Identify all requests by the title of the information collection. SUPPLEMENTARY INFORMATION: Description: OPRE is conducting the BIAS–NG project, which uses behavioral insights to design and test interventions intended to improve the efficiency, operations, and efficacy of human services programs. The BIAS– NG project is applying and testing behavioral insights to ACF programs including TANF, child welfare, and EHS/HS, and intends to expand these efforts to child care. This notice is a request for comments on ACF’s proposal to revise and extend a previously approved collection, which included data collection to design and test interventions in the TANF, child welfare, and EHS/HS domains. Under the approved pilot generic clearance, OPRE has already conducted work with seven sites to conduct seven tests, and is planning to continue to work with at least one additional site, conducting one or more tests of behavioral interventions for a total of nine tests of behavioral interventions. All approved information collection activities can be found here: https://www.reginfo.gov/public/do/ PRAICList?ref_nbr=202206-0970-002. In addition to extending approval, this approval would also allow OPRE to conduct tests in the newly added program area of child care. The design and testing of BIAS–NG interventions is rapid and, to the extent possible, iterative. Each specific intervention is designed in consultation with agency leaders and launched as quickly as possible. To maximize the likelihood that the intervention produces measurable, significant, and positive effects on outcomes of interest, rapid cycle evaluation techniques will be employed in which proximate outcomes will be measured to allow the research team to more quickly iterate and adjust the intervention design, informing subsequent tests. Due to the rapid and iterative nature of this work, OPRE sought and received approval for an overarching generic clearance to conduct this research. Following standard OMB requirements for generic clearances, once instruments subject to PRA are tailored to a specific site and the site’s intervention, OPRE submits an individual generic information collection request under this umbrella clearance. Each request includes the individual instrument(s), a justification specific to the individual information collection, a description of the proposed intervention, and any supplementary documents. Each specific information collection includes up to two submissions—one submission for the formative stage research and another submission for any further data collection requiring burden during the testing phase. The type of information to be collected and the uses of the information is described in the supporting statements, found here: https://www.reginfo.gov/public/do/ PRAViewDocument?ref_nbr=2022060970-002. Respondents: (1) Program Administrators, (2) Program Staff, and (3) Program Clients. ANNUAL BURDEN ESTIMATES [TANF, child welfare, EHS/HS, child care] Number of respondents (TANF, CW, EHS/HS, CC) (total over request period) Instrument Number of responses per respondent (total over request period) Average burden per response (in hours) Total burden (in hours) Annual burden (in hours) Phase 3: Diagnosis and Design ddrumheller on DSK120RN23PROD with NOTICES1 Administrator interviews/focus groups ................................. Staff interviews/focus groups ............................................... Client interviews/focus groups ............................................. Client survey ........................................................................ Staff Survey ......................................................................... 48 400 400 400 400 1 1 1 1 1 1 1 1 .25 .25 48 400 400 100 100 16 133 133 33 33 1 1 1 1 1 1 1 1 .25 .25 96 800 800 3,000 300 32 267 267 1,000 100 Phase 4: Evaluation Administrator interviews/focus groups ................................. Staff interviews/focus groups ............................................... Client interviews/focus groups ............................................. Client survey ........................................................................ Staff Survey ......................................................................... VerDate Sep<11>2014 18:22 Aug 13, 2024 Jkt 262001 PO 00000 Frm 00087 96 800 800 12,000 1,200 Fmt 4703 Sfmt 4703 E:\FR\FM\14AUN1.SGM 14AUN1 Federal Register / Vol. 89, No. 157 / Wednesday, August 14, 2024 / Notices Electronic Submissions Estimated Total Annual Burden Hours: 2,014. Authority: 42 U.S.C. 1310. Mary C. Jones, ACF/OPRE Certifying Officer. [FR Doc. 2024–18065 Filed 8–13–24; 8:45 am] BILLING CODE 4184–07–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. FDA–2024–N–3677] International Drug Scheduling; Single Convention on Narcotic Drugs; Convention on Psychotropic Substances; Hexahydrocannabinol; NPyrrolidino Protonitazene (Protonitazepyne); N-Pyrrolidino Metonitazene (Metonitazepyne); NPiperidinyl Etonitazene (Etonitazepipne); N-Desethylisotonitazene; 3-Hydroxyphencyclidine; N-Ethylheptedrone; Carisoprodol; Request for Comments AGENCY: Food and Drug Administration, HHS. ACTION: Notice; request for comments. ddrumheller on DSK120RN23PROD with NOTICES1 Written/Paper Submissions The Food and Drug Administration (FDA or Agency) is inviting interested persons to submit comments concerning abuse potential, actual abuse, medical usefulness, trafficking, and impact of scheduling changes on availability for medical use of eight drug substances. These comments will be considered in preparing a response from the United States to the World Health Organization (WHO) regarding the abuse liability and diversion of these drugs. WHO will use this information to consider whether to recommend that certain international restrictions be placed on these drug substances. This notice requesting comments is required by the Controlled Substances Act (CSA). DATES: Either electronic or written comments must be submitted by August 23, 2024. ADDRESSES: You may submit comments as follows. Please note that late, untimely filed comments will not be considered. The https:// www.regulations.gov electronic filing system will accept comments until 11:59 p.m. Eastern Time at the end of August 21, 2024. Comments received by mail/hand delivery/courier (for written/ paper submissions) will be considered timely if they are received on or before that date. SUMMARY: VerDate Sep<11>2014 18:22 Aug 13, 2024 Jkt 262001 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 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’’). 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– 2024–N–3677 for ‘‘International Drug Scheduling; Single Convention on Narcotic Drugs; Convention on Psychotropic Substances; Hexahydrocannabinol (HHC); NPyrrolidino Protonitazene (Protonitazepyne); N-Pyrrolidino Metonitazene (Metonitazepyne); NPiperidinyl Etonitazene (Etonitazepipne); N-Desethylisotonitazene; 3-Hydroxy-phencyclidine (3–OH–PCP); N-Ethylheptedrone; Carisoprodol; Request for Comments’’ 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 PO 00000 Frm 00088 Fmt 4703 Sfmt 4703 66117 Dockets Management Staff between 9 a.m. and 4 p.m., Monday through Friday, 240–402–7500. • Confidential Submissions—To submit a comment with confidential information that you do not wish to be made publicly available, submit your comments only as a written/paper submission. You should submit two copies total. One copy will include the information you claim to be confidential with a heading or cover note that states ‘‘THIS DOCUMENT CONTAINS CONFIDENTIAL INFORMATION.’’ The Agency will review this copy, including the claimed confidential information, in its consideration of comments. The second copy, which will have the claimed confidential information redacted/blacked out, will be available for public viewing and posted on https://www.regulations.gov. Submit both copies to the Dockets Management Staff. If you do not wish your name and contact information to be made publicly available, you can provide this information on the cover sheet and not in the body of your comments and you must identify this information as ‘‘confidential.’’ Any information marked as ‘‘confidential’’ will not be disclosed except in accordance with 21 CFR 10.20 and other applicable disclosure law. For more information about FDA’s posting of comments to public dockets, see 80 FR 56469, September 18, 2015, or access the information at: https:// www.govinfo.gov/content/pkg/FR-201509-18/pdf/2015-23389.pdf. Docket: For access to the docket to read background documents or the electronic and written/paper comments received, go to https:// www.regulations.gov and insert the docket number, found in brackets in the heading of this document, into the ‘‘Search’’ box and follow the prompts and/or go to the Dockets Management Staff, 5630 Fishers Lane, Rm. 1061, Rockville, MD 20852, 240–402–7500. FOR FURTHER INFORMATION CONTACT: Edward (Greg) Hawkins, Center for Drug Evaluation and Research, Controlled Substance Staff, Food and Drug Administration, 10903 New Hampshire Ave., Bldg. 51, Rm. 5110, Silver Spring, MD 20993–0002, 301–796–0727, edward.hawkins@fda.hhs.gov. SUPPLEMENTARY INFORMATION: I. Background The United States is a party to the 1971 Convention on Psychotropic Substances (Psychotropic Convention). Article 2 of the Psychotropic Convention provides that if a party to the convention or WHO has information about a substance, which in its opinion E:\FR\FM\14AUN1.SGM 14AUN1

Agencies

[Federal Register Volume 89, Number 157 (Wednesday, August 14, 2024)]
[Notices]
[Pages 66115-66117]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-18065]


=======================================================================
-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Administration for Children and Families


Submission for Office of Management and Budget Review; Behavioral 
Interventions To Advance Self-Sufficiency-Next Generation (BIAS-NG) 
(Office of Management and Budget #0970-0502)

AGENCY: Office of Planning, Research, and Evaluation, Administration 
for Children and Families, U.S. Department of Health and Human 
Services.

ACTION: Request for public comments.

-----------------------------------------------------------------------

SUMMARY: The Office of Planning, Research, and Evaluation (OPRE) in the 
Administration for Children and Families (ACF), U.S. Department of 
Health and Human Services (HHS) requests Office of Management and 
Budget (OMB) approval to modify and extend the approval of the ACF 
Behavioral Interventions to Advance

[[Page 66116]]

Self-Sufficiency-Next Generation (BIAS-NG) Project Overarching Generic 
(OMB #: 0970-0502; Expiration date: 8/31/2025.) Under this overarching 
clearance, ACF collects data as part of rapid cycle testing and 
evaluation, to inform the design of interventions informed by 
behavioral science and to better understand the mechanisms and effects 
of such interventions. Interventions have been and will continue to be 
developed in the program area domains of Temporary Assistance for Needy 
Families (TANF), child welfare, and Early Head Start/Head Start (EHS/
HS). This revision would also allow for collection of data in the child 
care program area, and would extend the approval of the overarching 
generic. These interventions are intended to improve outcomes for 
participants in these programs.

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. You can 
also obtain copies of the proposed collection of information by 
emailing [email protected]. Identify all requests by the 
title of the information collection.

SUPPLEMENTARY INFORMATION: 
    Description: OPRE is conducting the BIAS-NG project, which uses 
behavioral insights to design and test interventions intended to 
improve the efficiency, operations, and efficacy of human services 
programs. The BIAS-NG project is applying and testing behavioral 
insights to ACF programs including TANF, child welfare, and EHS/HS, and 
intends to expand these efforts to child care. This notice is a request 
for comments on ACF's proposal to revise and extend a previously 
approved collection, which included data collection to design and test 
interventions in the TANF, child welfare, and EHS/HS domains. Under the 
approved pilot generic clearance, OPRE has already conducted work with 
seven sites to conduct seven tests, and is planning to continue to work 
with at least one additional site, conducting one or more tests of 
behavioral interventions for a total of nine tests of behavioral 
interventions. All approved information collection activities can be 
found here: https://www.reginfo.gov/public/do/PRAICList?ref_nbr=202206-0970-002.
    In addition to extending approval, this approval would also allow 
OPRE to conduct tests in the newly added program area of child care. 
The design and testing of BIAS-NG interventions is rapid and, to the 
extent possible, iterative. Each specific intervention is designed in 
consultation with agency leaders and launched as quickly as possible. 
To maximize the likelihood that the intervention produces measurable, 
significant, and positive effects on outcomes of interest, rapid cycle 
evaluation techniques will be employed in which proximate outcomes will 
be measured to allow the research team to more quickly iterate and 
adjust the intervention design, informing subsequent tests. Due to the 
rapid and iterative nature of this work, OPRE sought and received 
approval for an overarching generic clearance to conduct this research. 
Following standard OMB requirements for generic clearances, once 
instruments subject to PRA are tailored to a specific site and the 
site's intervention, OPRE submits an individual generic information 
collection request under this umbrella clearance. Each request includes 
the individual instrument(s), a justification specific to the 
individual information collection, a description of the proposed 
intervention, and any supplementary documents. Each specific 
information collection includes up to two submissions--one submission 
for the formative stage research and another submission for any further 
data collection requiring burden during the testing phase. The type of 
information to be collected and the uses of the information is 
described in the supporting statements, found here: https://www.reginfo.gov/public/do/PRAViewDocument?ref_nbr=202206-0970-002.
    Respondents: (1) Program Administrators, (2) Program Staff, and (3) 
Program Clients.

                                             Annual Burden Estimates
                                    [TANF, child welfare, EHS/HS, child care]
----------------------------------------------------------------------------------------------------------------
                                     Number of       Number of
                                    respondents    responses per
                                  (TANF, CW, EHS/   respondent    Average burden   Total burden    Annual burden
           Instrument             HS, CC) (total    (total over    per response     (in hours)      (in hours)
                                   over request       request       (in hours)
                                      period)         period)
----------------------------------------------------------------------------------------------------------------
                                          Phase 3: Diagnosis and Design
----------------------------------------------------------------------------------------------------------------
Administrator interviews/focus                48               1               1              48              16
 groups.........................
Staff interviews/focus groups...             400               1               1             400             133
Client interviews/focus groups..             400               1               1             400             133
Client survey...................             400               1             .25             100              33
Staff Survey....................             400               1             .25             100              33
----------------------------------------------------------------------------------------------------------------
                                               Phase 4: Evaluation
----------------------------------------------------------------------------------------------------------------
Administrator interviews/focus                96               1               1              96              32
 groups.........................
Staff interviews/focus groups...             800               1               1             800             267
Client interviews/focus groups..             800               1               1             800             267
Client survey...................          12,000               1             .25           3,000           1,000
Staff Survey....................           1,200               1             .25             300             100
----------------------------------------------------------------------------------------------------------------


[[Page 66117]]

    Estimated Total Annual Burden Hours: 2,014.
    Authority: 42 U.S.C. 1310.

Mary C. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2024-18065 Filed 8-13-24; 8:45 am]
BILLING CODE 4184-07-P


This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.