# Agency Information Collection Activities: Proposed Collection: Public Comment Request; Information Collection Request Title: Health Resources and Services Administration Uniform Data System
**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 February 9, 2026.
**ADDRESSES:**
Submit your comments to *[email protected]* or mail the HRSA Information Collection Clearance Officer, Room 13N82, 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 Samantha Miller, 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:* Health Resources and Services Administration (HRSA) Uniform Data System (UDS), OMB No. 0915-0193 − Revision
*Abstract:* The Health Center Program, administered by HRSA, is authorized under section 330 of the Public Health Service (PHS) Act (42 U.S.C. 254b). Health centers are community-based and patient-directed organizations that deliver affordable, accessible, quality, and cost-effective primary health care services to patients regardless of their ability to pay. Nearly 1,400 funded health centers operate more than 16,200 service delivery sites that provide primary health care to more than 32 million people in every U.S. state, the District of Columbia, Puerto Rico, the U.S. Virgin Islands, and the Pacific Basin.
HRSA uses the UDS for annual reporting of program-specific data by Health Center Program awardees (those funded under section 330 of the PHS Act), Health Center Program look-alikes (entities meeting requirements of, but not funded under, section 330 of the PHS Act), and Nurse Education, Practice, Quality and Retention (NEPQR) and Advanced Nursing Education (ANE) Program awardees (specifically those funded under the practice priority areas of sections 831(b) and 811 of the PHS Act).
Some NEPQR and ANE Program awardees establish and expand nursing practice arrangements in non-institutional settings to demonstrate methods for improving access to primary health care in medically underserved communities. Nursing grantees implementing nursing practice arrangements have historically used the same data collection system as the Health Center Program.
*Need and Proposed Use of the Information:* HRSA requires the collection of information through UDS to monitor and evaluate the performance of health centers under section 330 and select NEPQR and ANE recipients under sections 831(b) and 811. These data support program compliance, inform quality improvement initiatives, guide the delivery of technical assistance, and shape federal health program decisions. To keep this instrument relevant and responsive to the Health Center Program's needs and Administration priorities, periodic updates are essential. HRSA proposes to make the following updates for the performance year 2026 UDS data collection:
**Table 4: Selected Patient Characteristics**
**Removal**
• Managed Care Utilization—UDS measures associated with managed care member months, *Capitated Member Months, Fee-for-Service Member Months,* and *Total Member Months* (Lines 13a-13c) will be removed to reduce the reporting burden, given variations in payer structures and payment arrangements across health centers.
**Table 6A: Selected Diagnoses and Services Rendered**
**Removals**
• *Various Clinical Measures* —Clinical measures associated with various diagnoses and selected services rendered are being removed from Table 6A to streamline reporting, reduce burden, and eliminate potential redundancies where similar information is captured elsewhere in the UDS. These updates align with the Administration and HRSA's priorities to simplify data collection and focus reporting on measures that provide the greatest programmatic value. The specific measures proposed for removal are indicated below:
• Novel coronavirus (SARS-CoV-2) disease (Line 4c)
• Long COVID (Line 4d)
• Respiratory conditions related to COVID-19 (Line 6a)
• Abnormal breast cancer findings, female (Line 7)
• Abnormal cervical findings (Line 8)
• Contact dermatitis and other eczema (Line 12)
• Novel coronavirus (SARS-CoV-2) diagnostic test (Line 21c)
• Novel coronavirus (SARS-COV-2) antibody test (Line 21d)
• Mammogram (Line 22)
• Pap test (Line 23)
• Sealants (Line 30)
• Oral surgery (extractions and other surgical procedures) (Line 33)
• Rehabilitative services (Endo, Perio, Prostho, Ortho) (Line 34)
**Additions**
• *Type I Diabetes* —A new measure is being added as line 9a to identify the number of patients with Type 1 Diabetes. This addition will help address key data gaps and improve HRSA's understanding of the distinct care and resource needs of patients with Type 1 Diabetes.
• *Intellectual and Developmental Disabilities* —A new measure is being added as line 20g to capture the number of patients with intellectual and developmental disabilities. Available data indicate that this population may experience lower rates of access to preventive and chronic care, including fewer screenings, lower dental care utilization, and higher rates of undiagnosed or unmanaged conditions. Capturing this information will improve understanding of the prevalence of persons with intellectual and developmental disabilities in the Health Center Program and support efforts to enhance health care access and quality of care for individuals requiring complex coordinated services.
• *Autism Spectrum Disorder Screening* —A new measure is being added as line 26g to capture the number of patients screened for autism spectrum disorder. This measure, in alignment with Administration priorities, will help assess the extent to which health centers are implementing recommended developmental screening practices and connecting children and families to needed support services.
• *Patient Support Services* —Four new measures are being added as lines 35-38 to capture the number of patients receiving case management, eligibility assistance, transportation, and language assistance services to better understand the range of non-clinical services that facilitate access to care and contribute to improved patient outcomes.
• *Health-Related Needs* —Four new measures are being added as lines 39-42, transitioning from Appendix D to the UDS core tables, to identify the number of patients who are screened for, and who receive, services addressing health-related needs. These or similar measures are now being elevated to the core reporting set to support standardized data collection. Integrating these measures within the core tables will enhance the ability to monitor how health centers identify and address patients' access to and utilization of services.
**Table 6B: Quality of Care Measures and Table 7: Health Outcomes**
**Updates**
• *Clinical Quality Measures* —Tables 6B and 7 collect UDS clinical quality measures, and where applicable, clinical quality measures will be updated in alignment with specifications of the issued performance year 2026 electronic clinical quality measures. These specifications were released by the Centers for Medicare & Medicaid Services on May 8, 2025, for use by eligible providers. Aligning clinical performance measures across national programs promotes data standardization, quality, and transparency, and decreases the reporting burden for providers and organizations participating in multiple federal programs.
**Table 8A: Financial Costs**
**Removals**
• *Allocation of Facility and Non-Clinical Support Services* —Allocation of Facility and Non-Clinical Support Services, Column b, and the requirement to report overhead costs on Table 8A will be removed.
• *Enabling Services* —Details for Cost of Enabling Services, Lines 11a, 11b, 11c, 11d, 11e, 11f, and 11h will be removed. These costs will be consolidated into a single line to reflect all Patient Support Services costs (previously known as Enabling Services).
• *Donations* —Line 18, Value of Donated Facilities, Services, and Supplies (specify __), will be removed.
These updates are being made to reduce the reporting burden, aligning with the Administration and HRSA's priorities and Health Center Program stakeholder feedback.
**Table 9D: Patient Service Revenue**
**Removals**
• *Retroactive Settlements, Receipts, and Paybacks* —measures associated with Columns c1—c4 for classification of collections will be removed:
• Collection of Reconciliation/Wraparound Current Year (c1)
• Collection of Reconciliation/Wraparound Previous Years (c2)
• Collection of Other Payments: Pay for Performance, Risk Pools, etc. (c3)
• Penalty/Payback (c4)
• *Payer Category* —Managed care lines have been consolidated as part of total payor revenue. *Total Medicaid* (Line 3), *Total Medicare* (Line 6), *Total Other Public* (specify) (Line 9), and *Total Private* (Line 12) will be reported, and the following lines will be removed as a result:
• Medicaid Non-Managed Care (Line 1)
• Medicaid Managed Care (capitated) (Line 2a)
• Medicaid managed Care (fee-for-service) (Line 2b)
• Medicare Non-Managed Care (Line 4)
• Medicare Managed Care (capitated) (Line 5a)
• Medicare Managed Care (fee-for service) (Line 5b)
• Other Public, including Non-Medicaid Children's Health Insurance Program (CHIP), Non-Managed Care (Line 7)
• Other Public, including Non-Medicaid CHIP, Managed Care (capitated) (Line 8a)
• Other Public, including Non-Medicaid CHIP, Managed Care (fee-for-service) (Line 8b)
• Private Non-Managed Care (Line 10)
• Private Managed Care (capitated) (Line 11a)
• Private Managed Care (fee-for-service) (Line 11b)
These updates are being made to reduce the reporting burden, aligning with the Administration and HRSA's priorities and stakeholder feedback.
**Additions**
• *Net Patient Services Revenue* —A new column will be added for *Net Patient Services Revenue* (charges less adjustments) (Line 16, Column g).
• *Pharmacy Net Patient Service Revenue* —A new line will be added to reflect all *Pharmacy Net Patient Service Revenue* (Line 17, Column g).
• *Third-Party Incentive Revenue* —A new line will be added for *Third-Party Incentive Revenue* (Line 18, Column g).
These updates are being made to reduce reporting burden and to better assess financials in alignment with generally accepted accounting principles.
**Table 9E: Other Revenue**
**Removals**
• *HRSA's Bureau of Primary Health Care (BPHC) Grants* —Health Center Program grant funding sources (formerly Lines 1a-1e) and other BPHC funding detail lines (formerly Lines 1o-1q) will be removed. Grants with active funding will be aggregated and reported on the *Total Health Center BPHC Grants* line (Line 1), while those no longer receiving funding will be excluded from reporting.
• *Other Federal Grants* —Other federal grant funding sources (formerly Lines 2 and 3) will be removed.
These updates are being made to align with supplemental funding being rolled into the base Health Center Program funding, as well as to remove outdated supplemental funding lines and reduce the reporting burden.
**Appendix D: Health Center Information Technology (Health IT) Capabilities and Appendix E: Other Data Elements**
**Removals**
• *Appendix D: Health IT Capabilities* —Several questions specific to Electronic Health Records implementation (Questions 1a, 1a2, 1a3, 1c, 1c1, and 10) will be removed from Appendix D.
• *Appendix D: Health IT Capabilities* —Health-related needs screening questions (Questions 11, 11a, 12, 12a, and 12b) will be removed from Appendix D.
• *Appendix E: Other Data Elements* —Appendix E will be removed, and certain data elements will be combined with Appendix D. Outreach and enrollment assists (formerly Appendix E, Question 3) will be removed (aspects will be incorporated in the Table 6A Patient Support Services addition).
These updates are being made to reduce the reporting burden, aligning with the Administration and HRSA's priorities and stakeholder feedback.
**Additions**
• *Appendix D: Health IT Capabilities* —Three questions on Alternative Payment Models (APM) will be added to Appendix D (Questions 17-19), to include:
• What payor arrangements do you have for value-based purchasing contracts?
• Please list the types of APMs your health center is involved in.
• What percentage of your health center's revenue during the year is tied to value-based payment contracts?
These additional data elements are being proposed to capture health centers' participation in APMs to improve understanding of the evolving payment landscape within the Health Center Program. As health centers increasingly engage in payment arrangements that emphasize value, care coordination, and outcomes rather than volume of services, collecting information on APM participation will provide valuable insight into the range and scope of these models.
*Likely Respondents:* Respondents will include Health Center Program award recipients and Health Center Program look-alikes carrying out programs under section 330 of the PHS Act and NEPQR and ANE award recipients funded under the practice priority areas of section 831(b) and 811 of the PHS Act.
*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.
*Total Estimated Annualized Burden Hours:*
| Form name | Number of respondents * | Number of | Total | Average | Total burden hours |
| --- | --- | --- | --- | --- | --- |
| UDS—Universal Report | Total: 1,605 | 1.00 | 1,605.00 | 185.08 | 297,053.40 |
| UDS Grant Report | Total: 419 | 1.22 | 511.18 | 20.80 | 10,632.54 |
| | Health Centers will submit one or more Grant Reports in 2026 | | | | |
| | 1 Grant Report: 337 | | | | |
| | 2 Grant Reports: 71 | | | | |
| | 3 Grant Reports: 11 | | | | |
| Total | 2,024.00 | | 2,116.18 | | 307,685.94 |
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.