Visual Plasticity Following Brain Lesions
Recruiting
N/A
Interventional Study
Visual Field Defect
Stroke
Hemianopia
Quadrantanopia
Cortical Blindness
Brain Tumor
Traumatic Brain Injury
Visual Field Defect, Peripheral
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
- 30 (estimated)
- Sponsor
- Georgetown University · Other
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About This Trial
The VIBRANT (Vision Improvement through Behavioral Rehabilitation And Neuroplasticity Training) study is a prospective, double-blind, crossover design (within-subject) in participants with homonymous hemianopia-a type of visual field loss resulting from damage to the post-chiasmatic visual pathways. It aims to investigate whether transcranial random noise stimulation (tRNS) combined with perceptua…
Trial Locations
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Eligibility Criteria
A. Stroke, brain tumor, or traumatic brain injury patients
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 loss of vision.
4. At least three months post-stroke or tr…
Contacts