Actively Recruiting
Biofeedback Training to Improve Fixation Stability, Visual Function Outcomes, and Quality of Life in Hemianopia Cases
Led by University Health Network, Toronto · Updated on 2025-05-29
70
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating the use of biofeedback training to help people with hemianopia, a vision loss in half of the visual field caused by brain injury such as stroke, surgery, or trauma. About 45% of stroke survivors have this condition, which can affect eye movements, reading ability, and spatial perception, impacting rehabilitation and daily life. The study aims to assess if biofeedback training can improve eye control, visual function, and quality of life for these patients. The study compares two groups: one receiving biofeedback training consisting of 20-minute sessions once a week for five weeks using a microperimeter device that provides light and sound stimulation to guide eye movements, and a control group that receives no intervention but undergoes the same assessments. After the training, participants have follow-up visits at 30 days, 6 months, and 1 year, while the control group is offered training after the study. The training helps the brain use the best remaining visual area and improves fixation stability and eye movement control. Participants will undergo various vision tests including retinal sensitivity, fixation stability, reading speed, contrast sensitivity, and visual acuity for distance and near vision. They also complete a quality of life questionnaire before and after the intervention. Assessments occur at baseline, post-treatment, and during follow-ups up to two years. The study carefully monitors eye movement patterns and vision function to evaluate the impact of biofeedback training on hemianopia patients.
CONDITIONS
Brief Title
Biofeedback Training for Hemianopia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Hemianopia diagnosed more than 6 months ago
- Age between 18 and 90 years
- Ability to follow visual and auditory training instructions
- Diagnosis confirmed by microperimetry or other tests
You will not qualify if you...
- Previous or current low vision rehabilitation treatment
- Presence of ocular diseases
- Serious health conditions unrelated to hemianopia
- Media opacity in both eyes preventing microperimetry testing
- Inability to perform required tests and training
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants undergo baseline assessments, including vision and eye movement tests, and are randomized to either the biofeedback training group or the control group.
1 visit (in-person)
Duration - 5 weeks
Participants in the treatment group attend weekly 20-minute biofeedback training sessions for 5 weeks to improve eye movement control and visual function.
5 weekly visits (in-person)
Duration - Up to 24 months
Participants return for follow-up visits to assess vision, eye movement, reading speed, and quality of life improvements after biofeedback training.
Visits at approximately 1 month, 6 months, 12 months, and 24 months post-treatment
Trial Site Locations
Total: 1 location
1
Toronto Western Hospital
Toronto, Ontario, Canada, M5T 2S8
Actively Recruiting
Research Team
M
Monica Daibert-Nido, MD
C
Clarice Mediana, Assistant
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
CROSSOVER
Primary Purpose
TREATMENT
Number of Arms
2
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