Agency Information Collection Activities: Proposed Collection: Public Comment Request; Information Collection Request Title: Behavioral Health Integration Evidence Based Telehealth Network Program Outcome Measures, 85545-85546 [2024-24962]

Download as PDF Federal Register / Vol. 89, No. 208 / Monday, October 28, 2024 / Notices 01/2020-07419/21st-century-cures-actinteroperability-information-blocking-andthe-onc-health-it-certification. 11 Office of the National Coordinator for Health IT. (2023). United States Core Data for Interoperability (USCDI). Retrieved from https://www.healthit.gov/isa/united-statescore-data-interoperability-uscdi. 12 Office of the National Coordinator for Health IT. (2023) United States Core (US Core) Fast Healthcare Interoperability Resources (FHIR) Retrieved from https:// hl7.org/fhir/us/core/history.html. 13 Office of the National Coordinator for Health IT. (2023) United States Core (US Core) Fast Healthcare Interoperability Resources (FHIR) Retrieved from https:// hl7.org/fhir/us/core/history.html. 14 Office of the National Coordinator for Health IT. (2023). United States Core Data for Interoperability. Retrieved from https:// www.healthit.gov/isa/sites/isa/files/2023-10/ USCDI-Version-4-October-2023-ErrataFinal.pdf. 15 Office of the National Coordinator for Health IT. (2023). United States Core Data for Interoperability Plus (USCDI+). Retrieved from https://www.healthit.gov/topic/ interoperability/uscdi-plus. 16 Office of Planning, Research and Evaluation an Office of the Administration of Children & Families. (2023). Human Services Interoperability Innovations (HSII). Retrieved from https://www.acf.hhs.gov/opre/project/ human-services-interoperability-innovationshsii-2020-2021. 17 Health Level Seven (HL7) Confluence. (2023). Human and Social Services Home. Retrieved from https://confluence.hl7.org/ display/HSS/ Human+and+Social+Services+Home. 18 Centers for Medicare & Medicaid Services. (2020). CMS Interoperability and Patient Access Final Rule (CMS–9115–F). Retrieved from https://www.cms.gov/ interoperability/policies-and-regulations/ cms-interoperability-and-patient-accessfinal-rule-cms-9115-f. 19 The Sequoia Project. (2022). FHIR Roadmap v1.0. Retrieved from https:// rce.sequoiaproject.org/wp-content/uploads/ 2022/01/FHIR-Roadmap-v1.0_updated.pdf. [FR Doc. 2024–24924 Filed 10–25–24; 8:45 am] BILLING CODE 4184–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES lotter on DSK11XQN23PROD with NOTICES1 Health Resources and Services Administration Agency Information Collection Activities: Proposed Collection: Public Comment Request; Information Collection Request Title: Behavioral Health Integration Evidence Based Telehealth Network Program Outcome Measures Health Resources and Services Administration (HRSA), Department of Health and Human Services. AGENCY: VerDate Sep<11>2014 19:13 Oct 25, 2024 Jkt 265001 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 December 27, 2024. ADDRESSES: Submit your comments to paperwork@hrsa.gov or mail the HRSA Information Collection Clearance Officer, Room 14NWH04, 5600 Fishers Lane, Rockville, Maryland, 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 Joella Roland, the HRSA Information Collection Clearance Officer, at (301) 443–3983. SUPPLEMENTARY INFORMATION: When submitting comments or requesting information, please include the ICR title for reference. Information Collection Request Title: Behavioral Health Integration Evidence Based Telehealth Network Program Outcome Measures, OMB No. 0906– xxxx—New. Abstract: This clearance request is for OMB approval of a new information collection, the Behavioral Health Integration Evidence Based Telehealth Network Program (BHI EB-TNP) Outcome Measures. Under the BHI EBTNP, HRSA administers grants in accordance with section 330I(d)(1) of the Public Health Service Act (42 U.S.C. 254c–14(d)(1)). The purpose of this program is to integrate behavioral health services into primary care settings using telehealth technology through telehealth networks and evaluate the effectiveness of such integration. This program supports evidence-based projects that utilize telehealth technologies through telehealth networks in rural and underserved areas to (1) improve access to integrated behavioral health services in primary care settings; and (2) expand and improve the quality of health information available to health care providers by evaluating the effectiveness of integrating telebehavioral health services into primary care settings and establishing SUMMARY: PO 00000 Frm 00058 Fmt 4703 Sfmt 4703 85545 an evidence-based model that can assist health care providers. HRSA created a set of outcome measures to evaluate the effectiveness of grantees’ services programs and monitor their progress using performance reporting data. The measures address behavioral health and substance use disorder priorities, originating and distant sites, specialties and services by site, volume of services by site and specialty, patient travel miles saved, and other uses of the telehealth network. Need and Proposed Use of the Information: HRSA’s goals for the program are to improve access to needed services, reduce rural practitioner isolation, improve health system productivity and efficiency, and improve patient outcomes. HRSA worked with program grantees to develop outcome measures to evaluate and monitor the progress of the grantees in each of these categories, with specific indicators to be reported annually through a performance monitoring data collection platform/website. Measures capture awardee-level and aggregate data that illustrate the impact and scope of program funding along with assessing these efforts. The measures are intended to inform HRSA’s progress toward meeting program goals, specifically improving access to telebehavioral health services that support primary care providers. Likely Respondents: BHI EB-TNP grantees. 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. E:\FR\FM\28OCN1.SGM 28OCN1 85546 Federal Register / Vol. 89, No. 208 / Monday, October 28, 2024 / Notices TOTAL ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Form name Total responses Average burden per response (in hours) Total burden hours BHI EB-TNP Outcome Measurement Report ...................... 27 1 27 5 135 Total .............................................................................. 27 ........................ 27 ........................ 135 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. 2024–24962 Filed 10–25–24; 8:45 am] BILLING CODE 4165–15–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health Submission for OMB Review; 30-Day Comment Request; Electronic Individual Development Plan (eIDP) (National Eye Institute) AGENCY: National Institutes of Health, HHS. ACTION: Notice. In compliance with the Paperwork Reduction Act of 1995, the National Institutes of Health (NIH) has submitted to the Office of Management and Budget (OMB) a request for review and approval of the information collection listed below. DATES: Comments regarding this information collection are best assured of having their full effect if received within 30-days of the date of this 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. FOR FURTHER INFORMATION CONTACT: To obtain a copy of the data collection plans and instruments, submit SUMMARY: lotter on DSK11XQN23PROD with NOTICES1 Number of responses per respondent VerDate Sep<11>2014 19:13 Oct 25, 2024 Jkt 265001 comments in writing, or request more information on the proposed project, contact: Dr. Cesar E. Perez-Gonzalez, Training Director, Office of the Scientific Director, National Eye Institute, NIH, Building 31, Room 6A22, MSC 0250, Bethesda, Maryland 20892 or call non-toll-free number (301) 451– 6763 or Email your request, including your address to: cesarp@nei.nih.gov. Formal requests for additional plans and instruments must be requested in writing. SUPPLEMENTARY INFORMATION: This proposed information collection was previously published in the Federal Register on August 1, 2024, 89 FR 62749 and allowed 60 days for public comment. No public comments were received. The purpose of this notice is to allow an additional 30 days for public comment. The National Eye Institute (NEI), National Institutes of Health, may not conduct or sponsor, and the respondent is not required to respond to, an information collection that has been extended, revised, or implemented on or after October 1, 1995, unless it displays a currently valid OMB control number. In compliance with Section 3507(a)(1)(D) of the Paperwork Reduction Act of 1995, the National Institutes of Health (NIH) has submitted to the Office of Management and Budget (OMB) a request for review and approval of the information collection listed below. Proposed Collection: Electronic Individual Development Plans, 0925– 0772 and 10/31/2024-Extension, National Eye Institute (NEI), National Institutes of Health (NIH). Need and Use of Information Collection: The National Eye Institute’s (NEI) Office of the Scientific Director (OSD) goal is to train the next generation of vision researchers and ophthalmologists. Trainees who participate in NEI research come with different levels of education (student, postbaccalaureate, predoctoral including graduate and medical students, postdoctoral fellows) and for different amounts of time (6 months to 5 years). Training at the NEI focuses on scientific and professional skill PO 00000 Frm 00059 Fmt 4703 Sfmt 4703 development. To enhance their chances of obtaining their ideal career, completing an annual Individual Development Plan (IDP) is an important step in helping a trainee’s career and professional development and is standard practice in graduate and postdoctoral education. An IDP is an effective tool for trainees to think about their career goals and skills needed to achieve them during their time at the NEI. Trainees work together with their research mentor to organize and summarize their research projects, consider career goals, and set training goals and expectations, both for the mentee and mentor. This information collection request is to implement an electronic Individual Development Plan (eIDP). The data collected comes from a detailed questionnaire focused on responses to professional goals and expectations while they are at the NEI. It is expected that the trainees will complete the eIDP annually and by doing so, it will help enhance the effectiveness of their training by setting clear goals that can be monitored not only by the trainee themselves but also by their mentor, the Training Director, and their Administrative Officer. In addition to this eIDP, the system will also implement an electronic exit survey. The data collected comes from a detailed questionnaire focused on responses to questions focused on trainee mentoring and professional experiences at the NEI as well as their plans after they depart. It is expected that the trainees will complete at the end of their tenure and that by doing so, the NEI Training Program can learn about ways to improve career development opportunities for future trainees as well as learn more about trainee job choices to better advise fellows. Additionally, we can use the survey to help determine mentor effectiveness and help identify problems in mentoring at the NEI. OMB approval is requested for 3 years. There are no costs to respondents other than their time. The total estimated annualized burden hours are 213. E:\FR\FM\28OCN1.SGM 28OCN1

Agencies

[Federal Register Volume 89, Number 208 (Monday, October 28, 2024)]
[Notices]
[Pages 85545-85546]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2024-24962]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Health Resources and Services Administration


Agency Information Collection Activities: Proposed Collection: 
Public Comment Request; Information Collection Request Title: 
Behavioral Health Integration Evidence Based Telehealth Network Program 
Outcome Measures

AGENCY: Health Resources and Services Administration (HRSA), Department 
of Health and Human Services.

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 December 
27, 2024.

ADDRESSES: Submit your comments to [email protected] or mail the HRSA 
Information Collection Clearance Officer, Room 14NWH04, 5600 Fishers 
Lane, Rockville, Maryland, 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 Joella Roland, the 
HRSA Information Collection Clearance Officer, at (301) 443-3983.

SUPPLEMENTARY INFORMATION: When submitting comments or requesting 
information, please include the ICR title for reference.
    Information Collection Request Title: Behavioral Health Integration 
Evidence Based Telehealth Network Program Outcome Measures, OMB No. 
0906-xxxx--New.
    Abstract: This clearance request is for OMB approval of a new 
information collection, the Behavioral Health Integration Evidence 
Based Telehealth Network Program (BHI EB-TNP) Outcome Measures. Under 
the BHI EB-TNP, HRSA administers grants in accordance with section 
330I(d)(1) of the Public Health Service Act (42 U.S.C. 254c-14(d)(1)). 
The purpose of this program is to integrate behavioral health services 
into primary care settings using telehealth technology through 
telehealth networks and evaluate the effectiveness of such integration. 
This program supports evidence-based projects that utilize telehealth 
technologies through telehealth networks in rural and underserved areas 
to (1) improve access to integrated behavioral health services in 
primary care settings; and (2) expand and improve the quality of health 
information available to health care providers by evaluating the 
effectiveness of integrating telebehavioral health services into 
primary care settings and establishing an evidence-based model that can 
assist health care providers. HRSA created a set of outcome measures to 
evaluate the effectiveness of grantees' services programs and monitor 
their progress using performance reporting data. The measures address 
behavioral health and substance use disorder priorities, originating 
and distant sites, specialties and services by site, volume of services 
by site and specialty, patient travel miles saved, and other uses of 
the telehealth network.
    Need and Proposed Use of the Information: HRSA's goals for the 
program are to improve access to needed services, reduce rural 
practitioner isolation, improve health system productivity and 
efficiency, and improve patient outcomes. HRSA worked with program 
grantees to develop outcome measures to evaluate and monitor the 
progress of the grantees in each of these categories, with specific 
indicators to be reported annually through a performance monitoring 
data collection platform/website. Measures capture awardee-level and 
aggregate data that illustrate the impact and scope of program funding 
along with assessing these efforts. The measures are intended to inform 
HRSA's progress toward meeting program goals, specifically improving 
access to telebehavioral health services that support primary care 
providers.
    Likely Respondents: BHI EB-TNP grantees.
    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.

[[Page 85546]]



                                     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
----------------------------------------------------------------------------------------------------------------
BHI EB-TNP Outcome Measurement                27               1              27               5             135
 Report.........................
                                 -------------------------------------------------------------------------------
    Total.......................              27  ..............              27  ..............             135
----------------------------------------------------------------------------------------------------------------

    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. 2024-24962 Filed 10-25-24; 8:45 am]
BILLING CODE 4165-15-P


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