Actively Recruiting

Phase Not Applicable
Age: 18Years - 90Years
All Genders
ID06995313

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

Age: 18Years - 90Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Baseline Assessment and Randomization

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)

Biofeedback Training

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)

Post-Treatment Follow-up

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

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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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