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Tests AI-assisted eye screening for glaucoma in community health clinic patients

Tests an AI tool to screen adults at clinics for glaucoma and other eye conditions.

Plain-language title generated from the registry record
Registry title: Implementing AI-based Glaucoma Screening Within Federally Qualified Health Centers

Key facts

Where
Birmingham, United StatesSee the site

Where in United States

  • Department of Ophthalmology and Visual Sciences, University of Alabama at BirminghamBirmingham, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
University of Alabama at Birmingham
Trial code
NCT06629649
Record updated
6 November 2026
Original description
The goal of this clinical trial is to learn if implementation of an eye screening program at Federally Qualified Health Center (FQHC) clinics provides results that participants may have glaucoma, and/or other eye conditions (diabetic retinopathy, cataract, visual acuity impairment). The glaucoma screening will incorporate use of an artificial intelligence (AI)-assisted screening tool. This project is called AI-RONA. The main questions it aims to answer are:Read full original descriptionShow less

Implementing AI-based Glaucoma Screening Within Federally Qualified Health Centers

The goal of this clinical trial is to learn if implementation of an eye screening program at Federally Qualified Health Center (FQHC) clinics provides results that participants may have glaucoma, and/or other eye conditions (diabetic retinopathy, cataract, visual acuity impairment). The glaucoma screening will incorporate use of an artificial intelligence (AI)-assisted screening tool. This project is called AI-RONA. The main questions it aims to answer are:

* How does this eye screening program compare to the rate of glaucoma and other eye conditions detected at other FQHC clinics where the screening program has not been implemented? * Do particpants who screen positive for these conditions adhere to the physician's recommendation for a follow-up examination by an optometrist or ophthalmologist? * Are referral rates for a follow-up comprehensive eye exam by an optometrist or ophthalmologist similar to those implemented by an ophthalmologist using telemedicine (that is, using the results of the screening to make a diagnosis remotely)? * What is the cost-effectiveness of the AI-assisted screening program in diagnosing glaucoma as compared to a physician-guided program? * Are participants completing the screening satisfied with it? * Are physicians at the FQHC clinics administering the screening satisfied with it?

Participants will:

* Undergo an ocular screening whose goal is to detect glaucoma, diabetic retinopathy, cataract, and/or impairment in visual acuity. If the screening indicates that participants may have these conditions, participants will be referred for a comprehensive eye examination by an optometrist or ophthalmologist. * Following the screening, participants and physicians will complete a survey on their satisfaction with the program.

Inclusion: African American or Hispanic persons ≥ 40 years old; Non-Hispanic white persons ≥ 50 years old; Anyone ≥ 18 years old with diabetes type 1 or type 2; Anyone ≥ 18 years old who already has a glaucoma associated disease; Anyone ≥ 18 years old with a family history of glaucoma.

Exclusion: Cannot communicate in English.

ClinicalTrials.gov NCT06629649