Home-based Vision Rehabilitation Guided by Brain Imaging

Purpose

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 pathways that support training-induced visual plasticity; and 2) compare the efficacy of different types of visual training delivered in a home-based setting.

Conditions

  • Visual Field Defect
  • Stroke
  • Hemianopia Homonymous
  • Quadrantanopia
  • Cortical Blindness
  • Visual Field Defect, Peripheral
  • Visual Field Loss
  • Traumatic Brain Injury
  • Brain Tumor

Eligibility

Eligible Ages
Over 18 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

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 past year. 5. Eligible for MRI based on standard safety screening.

Exclusion Criteria

  1. Severe neurological or psychiatric conditions unrelated to the focal lesion that may interfere with study participation or data interpretation. 2. Current or recent (within the past 6 months) drug or alcohol abuse or addiction as defined by DSM-5. 3. Ocular disease or disorder.

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Crossover Assignment
Intervention Model Description
Study Procedures Week 1: Pre-intervention visual assessment and functional magnetic resonance imaging (fMRI) scan (in-person study visit). Weeks 2-4: Participants complete at-home, online perceptual learning training using either low-level or high-level visual stimuli. End of Week 4: Online assessment to evaluate the spatial transfer of training effects. Weeks 5-6: Washout period to minimize potential carryover effects. Weeks 7-9: Participants complete the alternate at-home, online perceptual learning training condition (low-level or high-level visual stimuli). End of Week 9: Second online assessment to evaluate the spatial transfer of training effects. Week 10 (Final Visit): Post-intervention visual assessment and fMRI scan (in-person study visit). Approximately Week 24: Follow-up visual assessment and fMRI scan (in-person study visit). The timing of study visits and training sessions may be adjusted as needed to accommodate participants' health status, scheduling needs, or o
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Perceptual learning-based training using high-level visual stimuli
A 3 week at-home online perceptual learning-based training using high-level visual stimuli.
  • Behavioral: High-level perceptual learning-based training
    Behavioral intervention consisting of repeated computerized visual discrimination tasks targeting higher-order visual processing
Active Comparator
Perceptual learning-based training using low-level visual stimuli
A 3 week at-home online perceptual learning-based training using low-level visual stimuli.
  • Behavioral: Low-level perceptual learning-based training
    behavioral intervention consisting of repeated computerized visual discrimination tasks targeting low-level visual processing

Recruiting Locations

Georgetown University Medical Center
Washington D.C., District of Columbia 20057
Contact:
Tina Liu, PhD
202-784-9949
vpplab@georgetown.edu

More Details

Status
Recruiting
Sponsor
Georgetown University

Study Contact

Tina Liu, PhD
2027849920
tina.liu@georgetown.edu