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Home-based Vision Rehabilitation Guided by Brain Imaging

Behavioral Rehabilitation Through Image-Guided Home-based Training

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07635329
Acronym
BRIGHT
Enrollment
100
Registered
2026-06-09
Start date
2026-07-23
Completion date
2030-03-31
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

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

Keywords

neuroplasticity, stroke, vision, TBI, brain tumor

Brief summary

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.

Interventions

BEHAVIORALHigh-level perceptual learning-based training

Behavioral intervention consisting of repeated computerized visual discrimination tasks targeting higher-order visual processing

BEHAVIORALLow-level perceptual learning-based training

behavioral intervention consisting of repeated computerized visual discrimination tasks targeting low-level visual processing

Sponsors

Georgetown University
Lead SponsorOTHER
American Heart Association
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

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 or scheduling needs.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
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.

Design outcomes

Primary

MeasureTime frameDescription
Change in high-level perceptual discrimination performanceWeek 2-4 or Week 7-9 of the study (depending on the order)Change in performance on an online computerized high-level perceptual discrimination task. Participants complete a computerized high-level perceptual discrimination task during a 3-week training period (5 days per week). Task difficulty is adaptively adjusted using a 3-up/1-down staircase procedure to estimate perceptual discrimination thresholds corresponding to approximately 75% accuracy.
Change in low-level perceptual discrimination performanceWeek 2-4 or Week 7-9 of the study (depending on the order)Change in performance on an online computerized low-level perceptual discrimination task. Participants complete a computerized high-level perceptual discrimination task during a 3-week training period (5 days per week). Task difficulty is adaptively adjusted using a 3-up/1-down staircase procedure to estimate perceptual discrimination thresholds corresponding to approximately 75% accuracy.

Countries

United States

Contacts

CONTACTTina Liu, PhD
tina.liu@georgetown.edu2027849920

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 15, 2026