Clinical trial Recruiting at 1 site Interventional Ages 18 to 90

Biofeedback training for vision loss after brain injury

Official title: Biofeedback Training to Improve Fixation Stability, Visual Function Outcomes, and Quality of Life in Hemianopia Cases

Run by University Health Network, Toronto · NCT06995313 · Data updated 2026-11-12

This study is testing if biofeedback training can help people with vision loss from brain injuries see better and improve their quality of life.

Quick facts

Study typeInterventional
Ages18 Years to 90 Years
SexAll
Enrollment70 (estimated)
SponsorUniversity Health Network, Toronto
Academic / other
Locations1 site (Toronto, Ontario)
StatusRecruiting
StartedDecember 8, 2021
Main results expectedJuly 8, 2026
Study endsJuly 8, 2026
Registry record updatedMay 29, 2025
Trial IDNCT06995313 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are individuals aged 18-90 with hemianopia diagnosed more than six months post-lesion.

Probably not a fit

Patients who have received previous treatment for low vision rehabilitation or have serious ocular diseases may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the effectiveness of biofeedback training on microperimetry in patients with hemianopia resulting from brain injuries. Participants will undergo five sessions of 20 minutes each, where they will be stimulated with light and sound to engage the best residual areas of their visual fields. Visual tests and quality of life questionnaires will be administered before and after the training to assess improvements. The goal is to enhance visual and spatial perception, which is often impaired in these patients.

Why it matters

Potential benefit: If successful, this approach could significantly improve visual function and quality of life for patients suffering from hemianopia.

How similar studies have gone: While there is limited large-scale research on biofeedback training for hemianopia, similar approaches in visual rehabilitation have shown promise in smaller studies.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

Hemianopia cases with more than 6 months from the date of the lesion, previously diagnosed accordingly by micro perimetry and other tests as needed, 18-90 years old, ability to follow the visual and auditory stimuli and training instructions.

Exclusion Criteria:

Previous or current treatment for low vision rehabilitation, ocular diseases, other serious clinical conditions not related to the hemianopia, both eyes with media opacity that impairs microperimetry testing, lack of ability to perform the tests and training.

Where it's running

  • Toronto Western Hospital
    Toronto, Ontario, Canada
    Recruiting

Study contacts

  • Principal investigator: MONICA Daibert Nido, Assistant — University Healt Network
  • Study coordinator: Monica Daibert-Nido, MD
  • Email: lowvisionuhn@gmail.com
  • Phone: 4166035800

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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  • Vision on the Road: rehabilitation to improve driving-related vision after stroke

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  • How vision can recover after an occipital stroke

    This project will use brain MRI and vision testing to see if patterns of residual brain tissue and prior or ongoing visual training relate to partial vision recovery in people with occipital stroke and homonymous field loss.

    Recruiting University of Rochester · Rochester, New York · NCT07134777

  • Improving vision after brain injury

    It tests whether gentle brain stimulation (transcranial random noise stimulation) plus visual training can help adults with homonymous hemianopia regain some of their lost visual field.

    Recruiting Georgetown University · Washington D.C., District of Columbia · NCT07105358

  • Monitoring beta-lactam antibiotics and kidney clearance in ICU patients with acute brain injury

    This project tries to see if checking kidney clearance together with blood drug levels can quickly identify ICU patients with acute brain injury who need higher doses of beta-lactam antibiotics.

    Recruiting Centre Hospitalier Universitaire de Nīmes · Nîmes · NCT06999161

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.