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Tests a program to sustain diabetic eye screening by video in rural clinics

Tests I-SITE, a program using remote eye imaging, in adults with diabetic retinopathy.

Plain-language title generated from the registry record
Registry title: I-TRUST: Implementation of Teleophthalmology in Rural Health Systems Study

Key facts

Where
Madison, United StatesSee the site

Where in United States

  • UW School of Medicine and Public HealthMadison, United StatesNo longer taking part

Questions to ask the study team

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  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 Wisconsin, Madison
Trial code
NCT05254535
Record updated
15 May 2026
Original description
This pragmatic clinical trial is being conducted to test the effectiveness of I-SITE (Implementation for Sustained Impact in Teleophthalmology), an implementation program to sustain increased diabetic eye screening rates using teleophthalmology in rural, multi-payer health systems. Up to 10 rural health systems providing teleophthalmology to 10,000 patients with diabetes and 100 clinical care personnel participating in the I-SITE intervention will be enrolled for up to 48 months.Read full original descriptionShow less

I-TRUST: Implementation of Teleophthalmology in Rural Health Systems Study

This pragmatic clinical trial is being conducted to test the effectiveness of I-SITE (Implementation for Sustained Impact in Teleophthalmology), an implementation program to sustain increased diabetic eye screening rates using teleophthalmology in rural, multi-payer health systems. Up to 10 rural health systems providing teleophthalmology to 10,000 patients with diabetes and 100 clinical care personnel participating in the I-SITE intervention will be enrolled for up to 48 months.

Inclusion: Health system serves rural patients as defined as those patients living in counties considered rural by the federal Office of Management and Budget (OMB); Health system has an active clinical teleophthalmology program providing diabetic eye screening in primary care prior to study randomization; Health system agrees to share de-identified patient data at the requested time intervals.

Exclusion: Health system does not serve a rural patient population; Health system has a diabetic eye screening rate of greater than 50% (e.g., above the national average) as it may limit the ability to measure improvement from I-SITE.

ClinicalTrials.gov NCT05254535