NCT07409077Recruiting
Efficacy of Biofeedback Training for Glaucoma
Efficacy of Biofeedback Training for Visual Function and Quality of Life in Glaucoma: A Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 13 Feb 2026
Brief summary (registry, in English)
This randomized controlled clinical trial evaluates the efficacy of visual biofeedback training on visual function and quality of life in individuals with glaucoma. Glaucoma is a progressive optic neuropathy that can lead to irreversible vision loss, including impaired fixation stability, reduced retinal sensitivity, and decreased functional vision. Biofeedback training is a visual rehabilitation technique designed to help patients improve fixation stability and optimize use of remaining visual function by training eye movements toward retinal areas with better sensitivity. Seventy participants with glaucoma will be randomized to either a biofeedback training intervention group or a control group. Visual function outcomes, including fixation stability, retinal sensitivity, visual acuity, reading speed, contrast sensitivity, and quality of life, will be assessed at baseline and follow-up visits. This study aims to determine whether biofeedback training can improve visual function and quality of life in patients with glaucoma.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 70 (estimated)
- First submitted
- 3 Feb 2026
- Start date
- 10 Feb 2026
- Primary completion date
- 30 Jan 2028
- Lead sponsor
- University Health Network, Toronto
- Diseases
- Glaucoma
- NCT number
- NCT07409077
What you commit to
- Study type: Interventional
- Planned participants: 70
- From 10 Feb 2026 to the primary completion date, 30 Jan 2028
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Prior or current low vision rehabilitation treatment.
Other illness
- Ocular diseases or severe clinical conditions unrelated to glaucoma
Other
- Media opacities that prevent reliable microperimetry testing in both eyes.
- Inability to perform study assessments or follow instructions for biofeedback training.
Who the study is looking for
- 18-95 years old.
- Glaucoma cases with adequate intraocular pressure control.
- Presence of paracentral scotomata within two degrees of fixation.
- Ability to follow instructions for biofeedback training.
Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University Health Network-Toronto Western Hospital Coordinator of this site? Confirm its status | Toronto | Canada | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.