Philadelphia Telemedicine Glaucoma Detection and Follow-Up Study
NCT02390245 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 906
Last updated 2022-08-22
Summary
The goal is to conduct a 5-year prospective, randomized controlled trial to test an innovative, community-based intervention using posterior and anterior fundus photography of the optic nerve and macula and intraocular eye pressure measurements to improve access and utilization of eye care to detect, treat, and manage high-risk patients with previously undiagnosed glaucoma and other eye diseases. Research shows that subject failure to attend follow-up eye care appointments diminishes any previous benefits of community screenings for glaucoma. Greater adherence to follow-up visits can reduce glaucomatous blindness.
Conditions
- Glaucoma
- Glaucoma Suspect
- Diabetic Retinopathy
- Ocular Hypertension
- Cataract
- Branch Retinal Vein Occlusion
- Branch Retinal Arterial Occlusion
- Central Retinal Vein Occlusion
- Central Retinal Artery Occlusion
- Epi-retinal Membrane
- Macular Degeneration
- Drusen
- Loss of Vision
Interventions
- OTHER
-
Free Eye Screenings
This group will receive free eye screening and follow-up comprehensive ophthalmic exam if recommended.
- OTHER
-
Enhanced Intervention
This group will receive ophthalmic referral and a navigator for assistance in scheduling appointments; confirming appointments via phone, mail, email and/or text message; arranging transportation through Customized Community Transportation (CCT) and Philadelphia Paratransit Service; and trained medical interpreters as needed.
- OTHER
-
Usual Care
This group will receive ophthalmic referral.
Sponsors & Collaborators
-
Centers for Disease Control and Prevention
collaborator FED -
Westat
collaborator OTHER -
Public Health Management Corporation
collaborator OTHER -
Philadelphia Department of Public Health
collaborator OTHER_GOV -
Health Federation of Philadelphia
collaborator OTHER -
Temple Physicians, Inc.
collaborator INDUSTRY -
Wills Eye
lead OTHER
Principal Investigators
-
L. J Katz, MD · Wills Eye Hospital
-
Lisa A Hark, PhD · Wills Eye Hospital
-
Julia A Haller, MD · Wills Eye Hospital
Study Design
- Allocation
- RANDOMIZED
- Purpose
- OTHER
- Masking
- SINGLE
- Model
- PARALLEL
Eligibility
- Min Age
- 40 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2014-09-30
- Primary Completion
- 2019-09-30
- Completion
- 2020-08-31
Countries
- United States
Study Locations
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