Agency Information Collection Activities: Proposed Collection: Public Comment Request Information Collection Request Title: Health Resources and Service Administration Uniform Data System, OMB No. 0915-0193-Revision, 29800-29801 [2018-13587]

Download as PDF 29800 Federal Register / Vol. 83, No. 123 / Tuesday, June 26, 2018 / Notices TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS—Continued Number of respondents Form name Number of responses per respondent Total responses Average burden per response (in hours) Total burden hours National Survey of Organ Donation Attitudes and Practices—Web Online Panel (English and Spanish Versions) .......................................................................... 8,000 1 8,000 .27 2,160 Total .............................................................................. 10,000 ........................ 10,000 ........................ 2,900 Amy P. McNulty, Acting Director, Division of the Executive Secretariat. [FR Doc. 2018–13590 Filed 6–25–18; 8:45 am] BILLING CODE 4165–15–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Health Resources and Services Administration Agency Information Collection Activities: Proposed Collection: Public Comment Request Information Collection Request Title: Health Resources and Service Administration Uniform Data System, OMB No. 0915– 0193—Revision Health Resources and Services Administration (HRSA), Department of Health and Human Services. ACTION: Notice. AGENCY: 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 must be received no later than August 27, 2018. ADDRESSES: Submit your comments to paperwork@hrsa.gov or mail the HRSA Information Collection Clearance Officer, Room 14N39, 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, HRSA Information Collection Clearance Officer at (301) 443–1984. SUPPLEMENTARY INFORMATION: When submitting comments or requesting information, please include the sradovich on DSK3GMQ082PROD with NOTICES SUMMARY: VerDate Sep<11>2014 17:24 Jun 25, 2018 Jkt 244001 information request collection title for reference. Information Collection Request Title: HRSA Uniform Data System (UDS), OMB No. 0915–0193—Revision. Abstract: HRSA utilizes the UDS for annual reporting by certain HRSA award recipients, including Health Center Program awardees (those funded under section 330 of the Public Health Service (PHS) Act), Health Center Program look-alikes, and Nurse Education, Practice, Quality and Retention (NEPQR) Program awardees (specifically those funded under the practice priority areas of section 831(b) of the PHS Act). Need and Proposed Use of the Information: HRSA collects UDS data annually to ensure compliance with legislative and regulatory requirements, improve clinical and operational performance, and report overall program accomplishments. These data help to identify trends over time, enabling HRSA to establish or expand targeted programs and to identify effective services and interventions that will improve the health of medically underserved communities. HRSA compares UDS data with other national health-related data sets to compare HRSA award recipient patient populations and the overall U.S. population. HRSA is considering several changes for 2019 UDS data collection: • Substance Use Disorder and Mental Health Services: Collect substance use disorder and mental health services by provider specialty to better assess which providers are delivering behavioral health services; support investments in these priority areas; and better describe comprehensive, integrated models of care. • Closing the Referral Loop: Receipt of Specialist Report (https:// ecqi.healthit.gov/ecqm/measures/ cms050v6t): Add a clinical quality measure from the Centers for Medicare and Medicaid Services (CMS) electronic-specified clinical quality measures to address care coordination. • Health Information Technology (health IT): Streamline and clarify PO 00000 Frm 00060 Fmt 4703 Sfmt 4703 health IT questions regarding utilization of health IT to include information sharing, patient engagement, quality improvement, and program evaluation and research. • Statin Therapy for the Prevention and Treatment of Cardiovascular Disease (https://ecqi.healthit.gov/ecqm/ measures/cms347v1): Replace the current non-specified Coronary Artery Disease measure with an e-specified measure that aligns with the Centers for Disease Control and Prevention and the CMS Million Hearts® clinical quality measures relating to statin therapy. • Telemedicine and Virtual Visits: Collect information on services provided via telemedicine or virtual visits by provider in order to capture the changing health care delivery landscape. • Tenure for Health Center Staff: Retire Table 5A related to the tenure for staff. • Workforce: Collect workforce related information, including workforce satisfaction and health professional training. Likely Respondents: The respondents will include Health Center Program awardees, Health Center Program lookalikes, and NEPQR Program awardees funded under the practice priority areas of section 831(b) of the PHS Act. Burden Statement: Burden includes 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, disclosing and providing information. It also accounts for time to train personnel, respond to a collection of information, search data sources, complete and review the collection of information, and transmit or otherwise disclose the information. The total annual burden hours estimated for this ICR are summarized in the table below. E:\FR\FM\26JNN1.SGM 26JNN1 29801 Federal Register / Vol. 83, No. 123 / Tuesday, June 26, 2018 / Notices TOTAL ESTIMATED ANNUALIZED BURDEN HOURS Number of respondents Form name Number of responses per respondent Total responses Average burden per response (in hours) Total burden hours Universal Report .................................................................. Grant Report ........................................................................ 1,471 504 1 1 1,471 504 223 30 328,033 15,120 Total .............................................................................. 1,975 ........................ 1,975 ........................ 343,153 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. Amy P. McNulty, Acting Director, Division of the Executive Secretariat. [FR Doc. 2018–13587 Filed 6–25–18; 8:45 a.m.] BILLING CODE 4165–15–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Heart, Lung, and Blood Institute; Notice of Closed Meetings sradovich on DSK3GMQ082PROD with NOTICES Pursuant to section 10(d) of the Federal Advisory Committee Act, as amended, notice is hereby given of the following meetings. The meetings will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant applications, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: National Heart, Lung, and Blood Institute Special Emphasis Panel; lncRNAs in HLBS Diseases. Date: August 17, 2018. Time: 8:30 a.m. to 5:00 p.m. Agenda: To review and evaluate grant applications. Place: Crowne Plaza Washington National Airport, 1480 Jefferson Davis Hwy, Arlington, VA 22202. Contact Person: Keith A. Mintzer, Ph.D., Scientific Review Officer, Office of Review Branch/DERA, National Heart, Lung, and Blood Institute, 6701 Rockledge Drive, Room VerDate Sep<11>2014 17:24 Jun 25, 2018 Jkt 244001 7186, Bethesda, MD 20892–7924, 301–594– 7947 mintzerk@nhlbi.nih.gov. Name of Committee: National Heart, Lung, and Blood Institute Special Emphasis Panel; MACS–WIHS DACC. Date: August 21, 2018. Time: 8:00 a.m. to 8:30 a.m. Agenda: To review and evaluate grant applications. Place: Hyatt Regency Bethesda, One Bethesda Metro Center, 7400 Wisconsin Avenue, Bethesda, MD 20814. Contact Person: Tony L. Creazzo, Ph.D., Scientific Review Officer, Office of Scientific Review/DERA, National Heart, Lung, and Blood Institute, National Institutes of Health, 6701 Rockledge Drive, Room 7180, Bethesda, MD 20892–7924, 301–827–7913, creazzotl@ mail.nih.gov. Name of Committee: National Heart, Lung, and Blood Institute Special Emphasis Panel; MACS–WIHS Clinical Research Sites. Date: August 21, 2018. Time: 8:30 a.m. to 5:00 p.m. Agenda: To review and evaluate grant applications. Place: Hyatt Regency Bethesda, One Bethesda Metro Center, 7400 Wisconsin Avenue, Bethesda, MD 20814. Contact Person: Tony L. Creazzo, Ph.D., Scientific Review Officer, Office of Scientific Review/DERA, National Heart, Lung, and Blood Institute, National Institutes of Health, 6701 Rockledge Drive, Room 7180, Bethesda, MD 20892–7924, 301–827–7913, creazzotl@ mail.nih.gov. (Catalogue of Federal Domestic Assistance Program Nos. 93.233, National Center for Sleep Disorders Research; 93.837, Heart and Vascular Diseases Research; 93.838, Lung Diseases Research; 93.839, Blood Diseases and Resources Research, National Institutes of Health, HHS) Dated: June 19, 2018. Michelle D. Trout, Program Analyst, Office of Federal Advisory Committee Policy. [FR Doc. 2018–13633 Filed 6–25–18; 8:45 am] BILLING CODE 4140–01–P DEPARTMENT OF HEALTH AND HUMAN SERVICES National Institutes of Health National Heart, Lung, and Blood Institute; Notice of Closed Meetings Pursuant to section 10(d) of the Federal Advisory Committee Act, as PO 00000 Frm 00061 Fmt 4703 Sfmt 4703 amended, notice is hereby given of the following meetings of the NHLBI Special Emphasis Panel. The meetings will be closed to the public in accordance with the provisions set forth in sections 552b(c)(4) and 552b(c)(6), Title 5 U.S.C., as amended. The grant applications and contract proposals and the discussions could disclose confidential trade secrets or commercial property such as patentable material, and personal information concerning individuals associated with the grant applications and contract proposals, the disclosure of which would constitute a clearly unwarranted invasion of personal privacy. Name of Committee: National Heart, Lung, and Blood Institute Special Emphasis Panel; Career Development Program to Promote Diversity in Health Research. Date: July 13, 2018. Time: 8:00 p.m. to 5:00 p.m. Agenda: To review and evaluate grant applications. Place: The William F. Bolger Center, 9600 Newbridge Drive, Potomac, MD 20854. Contact Person: Michael P. Reilly, Ph.D., Scientific Review Officer, Office of Scientific Review, National Heart, Lung, and Blood Institute, National Institutes of Health, 6701 Rockledge Drive, Room 7200, Bethesda, MD 20892, 301–827–7975, reillymp@ nhlbi.nih.gov. Name of Committee: National Heart, Lung, and Blood Institute, Special Emphasis Panel; Short-term Research Education to Increase Diversity. Date: July 20, 2018. Time: 8:00 p.m. to 5:00 p.m. Agenda: To review and evaluate grant applications. Place: The William F. Bolger Center, 9600 Newbridge Drive, Potomac, MD 20854. Contact Person: Lindsay M. Garvin, Ph.D., Scientific Review Officer, Office of Scientific Review, National Heart, Lung, and Blood Institute, National Institutes of Health, 6701 Rockledge Drive, Suite 7189, Bethesda, MD 20892, 301–827–7911, lindsay.garvin@ nih.gov. Name of Committee: National Heart, Lung, and Blood Institute Special Emphasis Panel; NHLBI Mentored Career Development Awards—K08 and K99. Date: July 25, 2018. Time: 1:00 p.m. to 3:00 p.m. Agenda: To review and evaluate grant applications. E:\FR\FM\26JNN1.SGM 26JNN1

Agencies

[Federal Register Volume 83, Number 123 (Tuesday, June 26, 2018)]
[Notices]
[Pages 29800-29801]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-13587]


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

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Health Resources and Services Administration


Agency Information Collection Activities: Proposed Collection: 
Public Comment Request Information Collection Request Title: Health 
Resources and Service Administration Uniform Data System, OMB No. 0915-
0193--Revision

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 must be received no later than August 27, 
2018.

ADDRESSES: Submit your comments to [email protected] or mail the HRSA 
Information Collection Clearance Officer, Room 14N39, 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, HRSA Information Collection Clearance Officer at (301) 443-
1984.

SUPPLEMENTARY INFORMATION: When submitting comments or requesting 
information, please include the information request collection title 
for reference.
    Information Collection Request Title: HRSA Uniform Data System 
(UDS), OMB No. 0915-0193--Revision.
    Abstract: HRSA utilizes the UDS for annual reporting by certain 
HRSA award recipients, including Health Center Program awardees (those 
funded under section 330 of the Public Health Service (PHS) Act), 
Health Center Program look-alikes, and Nurse Education, Practice, 
Quality and Retention (NEPQR) Program awardees (specifically those 
funded under the practice priority areas of section 831(b) of the PHS 
Act).
    Need and Proposed Use of the Information: HRSA collects UDS data 
annually to ensure compliance with legislative and regulatory 
requirements, improve clinical and operational performance, and report 
overall program accomplishments. These data help to identify trends 
over time, enabling HRSA to establish or expand targeted programs and 
to identify effective services and interventions that will improve the 
health of medically underserved communities. HRSA compares UDS data 
with other national health-related data sets to compare HRSA award 
recipient patient populations and the overall U.S. population.
    HRSA is considering several changes for 2019 UDS data collection:
     Substance Use Disorder and Mental Health Services: Collect 
substance use disorder and mental health services by provider specialty 
to better assess which providers are delivering behavioral health 
services; support investments in these priority areas; and better 
describe comprehensive, integrated models of care.
     Closing the Referral Loop: Receipt of Specialist Report 
(https://ecqi.healthit.gov/ecqm/measures/cms050v6t): Add a clinical 
quality measure from the Centers for Medicare and Medicaid Services 
(CMS) electronic-specified clinical quality measures to address care 
coordination.
     Health Information Technology (health IT): Streamline and 
clarify health IT questions regarding utilization of health IT to 
include information sharing, patient engagement, quality improvement, 
and program evaluation and research.
     Statin Therapy for the Prevention and Treatment of 
Cardiovascular Disease (https://ecqi.healthit.gov/ecqm/measures/cms347v1): Replace the current non-specified Coronary Artery Disease 
measure with an e-specified measure that aligns with the Centers for 
Disease Control and Prevention and the CMS Million Hearts[reg] clinical 
quality measures relating to statin therapy.
     Telemedicine and Virtual Visits: Collect information on 
services provided via telemedicine or virtual visits by provider in 
order to capture the changing health care delivery landscape.
     Tenure for Health Center Staff: Retire Table 5A related to 
the tenure for staff.
     Workforce: Collect workforce related information, 
including workforce satisfaction and health professional training.
    Likely Respondents: The respondents will include Health Center 
Program awardees, Health Center Program look-alikes, and NEPQR Program 
awardees funded under the practice priority areas of section 831(b) of 
the PHS Act.
    Burden Statement: Burden includes 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, disclosing and providing 
information. It also accounts for time to train personnel, respond to a 
collection of information, search data sources, complete and review the 
collection of information, and transmit or otherwise disclose the 
information. The total annual burden hours estimated for this ICR are 
summarized in the table below.

[[Page 29801]]



                                     Total Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                      Average
                                     Number of       Number of         Total        burden per     Total  burden
            Form name               respondents    responses per     responses     response  (in       hours
                                                    respondent                        hours)
----------------------------------------------------------------------------------------------------------------
Universal Report................           1,471               1           1,471             223         328,033
Grant Report....................             504               1             504              30          15,120
                                 -------------------------------------------------------------------------------
    Total.......................           1,975  ..............           1,975  ..............         343,153
----------------------------------------------------------------------------------------------------------------

    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.

Amy P. McNulty,
Acting Director, Division of the Executive Secretariat.
[FR Doc. 2018-13587 Filed 6-25-18; 8:45 a.m.]
 BILLING CODE 4165-15-P