Home-based Vision Rehabilitation for Visual Field Loss
Home-based Vision Rehabilitation Guided by Brain Imaging
Recruiting
N/A
Interventional Study
Visual Field Defect
Stroke
Hemianopia Homonymous
Quadrantanopia
Cortical Blindness
Visual Field Defect, Peripheral
Visual Field Loss
Traumatic Brain Injury
Brain Tumor
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 100 (estimated)
- Sponsor
- Georgetown University · Other
Who this trial is looking for
This trial is looking for adults with visual field loss due to brain damage. Participants will undergo training at home guided by brain imaging to improve their vision.
Are You a Good Fit for This Trial?
You may be able to join if
- I am at least 18 years old.
- I can provide informed consent.
- I have brain damage causing visual field loss.
- I am at least three months post-stroke or brain injury.
- I have a stable brain tumor within the past year.
- I am eligible for an MRI.
You may not be able to join if
- I have severe neurological or psychiatric conditions unrelated to my brain damage.
- I have had drug or alcohol abuse or addiction in the past 6 months.
- I have an eye disease or disorder.
Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
Check Your Eligibility
About This Trial
The BRIGHT (Behavioral Rehabilitation Through Image-Guided Home-based Training) study aims to evaluate the effectiveness of image-guided, home-based perceptual training at improving visual performance in individuals with visual field loss.
Using a prospective, crossover design, BRIGHT combines visual behavioral testing, neuroimaging, and a home-based intervention. It aims to 1) identify neural pa…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. At least 18 years of age.
2. Capable of providing informed consent and complying with study procedures.
3. Unilateral or bilateral focal brain damage causing visual field loss.
4. At least three months post-stroke or traumatic brain injury, or a stable brain tumor within the …
Contacts