Clinical trial Recruiting at 1 site Interventional

Biofeedback training to improve vision in glaucoma

Official title: Efficacy of Biofeedback Training for Visual Function and Quality of Life in Glaucoma: A Randomized Controlled Trial

Run by University Health Network, Toronto · NCT07409077 · Data updated 2026-11-12

This study will test whether short sessions of visual biofeedback training can help people with glaucoma improve fixation stability, retinal sensitivity, and everyday vision.

Quick facts

Study typeInterventional
SexAll
Enrollment70 (estimated)
SponsorUniversity Health Network, Toronto
Academic / other
Locations1 site (Toronto, Ontario)
StatusRecruiting
StartedFebruary 10, 2026
Main results expectedJanuary 30, 2028
Study endsJune 2028
Registry record updatedFebruary 13, 2026
Trial IDNCT07409077 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18–95 with a diagnosis of glaucoma, controlled intraocular pressure, paracentral scotomata within two degrees of fixation, and the ability to follow training instructions are the intended participants.

Probably not a fit

People with other significant ocular disease, media opacities that prevent reliable testing, prior low-vision rehabilitation, or who cannot perform study assessments are unlikely to benefit from or be eligible for this intervention.

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

What this trial studies

This is a randomized controlled trial that will enroll 70 adults with glaucoma and paracentral scotomata and assign them 1:1 to either five weekly biofeedback training sessions or a control group receiving standard assessments. The intervention uses visual and auditory feedback during microperimetry to train eye movements toward retinal areas with better sensitivity and stability, with each session lasting about 20 minutes. Outcomes including fixation stability, retinal sensitivity, visual acuity, reading speed, contrast sensitivity, and vision-related quality of life will be measured at baseline and follow-up visits. The control group will be offered the training after completion of their study participation.

Why it matters

Potential benefit: If successful, biofeedback training could help people with glaucoma make better use of their remaining vision and improve daily tasks like reading and mobility.

How similar studies have gone: Some small studies of visual biofeedback in other retinal conditions and low-vision populations have shown improvements in fixation and function, but evidence specifically in glaucoma is limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* 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.

Exclusion Criteria:

* Prior or current low vision rehabilitation treatment.
* Ocular diseases or severe clinical conditions unrelated to glaucoma
* Media opacities that prevent reliable microperimetry testing in both eyes.
* Inability to perform study assessments or follow instructions for biofeedback training.

Where it's running

  • University Health Network/ Toronto Western Hospital
    Toronto, Ontario, Canada
    Recruiting

Similar studies

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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.