Actively Recruiting
Assessing the Impact of eSight Go At-Home Usage in Individuals With Visual Impairment
Led by Brooks Rehabilitation · Updated on 2025-08-29
50
Participants Needed
1
Research Sites
49 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to test the updated version of Gentex's device, eSight Go, an image enhancing wearable device to assist those with vision impairments limiting activities of daily living.
CONDITIONS
Official Title
Assessing the Impact of eSight Go At-Home Usage in Individuals With Visual Impairment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 18 to 90.
- Best-corrected visual acuity between 20/50 to 20/400 in the better eye.
- Diagnosed with an ocular condition causing visual impairment.
- Functional binocular field of view of at least 20 degrees.
- Stable visual status for at least six months.
- Demonstrate visual benefit from magnification.
- Agree to wear the eSight Go in various home and community situations.
- Score 20 or higher on the Short Orientation-Memory-Concentration Test of Cognitive Impairment (OMCT).
- Able to provide informed consent.
- Agree to use eSight Eyewear only under safe conditions that do not risk user or device safety.
You will not qualify if you...
- Currently undergoing medical or surgical procedures causing unstable vision.
- Had cataract, refractive, or other eye surgeries within six months before enrollment.
- Severe visual impairment worse than 20/400 in the better seeing eye.
- Cognitive limitations with OMCT score below 20.
- Received vision-related injections (e.g., anti-VEGF) in the two months before the study due to active retinal bleeding; ongoing anti-VEGF treatments allowed if disease is stable.
- Unable or unwilling to follow study examination schedules or travel requirements.
- History of alcoholism, drug abuse, or psychosis.
- Clinical signs of depression, poor motivation, emotional or intellectual issues limiting valid consent or participation.
- Potential conflicts of interest with eSight Corp affecting participation.
- Refractive error outside the range correctable by the device's lens inserts (greater than +/-8.00 diopters spherical or -4.00 diopters cylindrical).
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Brooks Rehabilitation
Jacksonville, Florida, United States, 32216
Actively Recruiting
Research Team
H
Hannah Grimes
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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