Restorative and compensatory therapy approaches in cerebral blindness - a review.
G Kerkhoff
https://pubmed.ncbi.nlm.nih.gov/12671237Actively Recruiting
Led by University Health Network, Toronto · Updated on 2025-05-09
32
Participants Needed
1
Research Sites
9 weeks
Total Duration
U
University Health Network, Toronto
Lead Sponsor
U
University of Toronto
Collaborating Sponsor
Researchers are studying the effects of biofeedback training (BT) on patients with homonymous hemianopia, a vision loss condition affecting one half of the visual field due to brain injury from stroke, surgery, or trauma. This condition often leads to difficulties in eye movements, reading, and spatial perception, which can slow rehabilitation progress. The study aims to systematically assess the impact of BT on vision rehabilitation and formulate guidelines for its use in hemianopia cases. The study involves training oculomotor functions using the biofeedback module of a microperimeter device called MAIA. Participants are randomly assigned to two groups: one receiving BT intervention and the other with no intervention initially. BT uses visual and auditory feedback to improve eye control, fixation stability, and reading ability by helping patients shift their gaze towards their blind visual field. The intervention includes about five weekly sessions of 20 minutes each. Participants undergo baseline assessments and are evaluated one week after the biofeedback sessions. Assessments include visual acuity, fixation stability, retinal sensitivity, reading speed, near vision, quality of life questionnaires, stereopsis, and contrast sensitivity. The study monitors how BT affects oculomotor control and vision-related quality of life, with a focus on improving patients' ability to navigate and read despite their visual field loss.
CONDITIONS
Biofeedback for Hemianopia Vision Rehabilitation
You may qualify if you...
You will not qualify if you...
Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 5 weeks
Participants in the experimental group receive biofeedback training to improve eye movement control using a microperimeter device, while participants in the control group undergo assessments without intervention.
Weekly visits for up to 5 weeks
Duration - 1 week
Participants are assessed one week after completing the biofeedback training to evaluate visual acuity, fixation stability, reading speed, and quality of life improvements.
1 visit (in-person)
Total: 1 location
1
Toronto Western Hospital
Toronto, Ontario, Canada, M5T2S8
Actively Recruiting
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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G Kerkhoff
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