Using virtual reality to measure progress during low vision rehabilitation
Official title: Validation of a Virtual Reality Test for the Assessment of Visually Impaired Patients Undergoing Low Vision Rehabilitation
Run by Fondation Ophtalmologique Adolphe de Rothschild · NCT07092124 · Data updated 2026-11-12
This project will test a 20-minute virtual reality test (VisionumVR on a Meta Quest 3) to measure functional vision in people with low vision who are starting or undergoing orthoptic rehabilitation.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Fondation Ophtalmologique Adolphe de Rothschild Research network |
| Locations | 2 sites (Angers and 1 other locations) |
| Status | Recruiting |
| Started | October 30, 2025 |
| Main results expected | February 2027 |
| Study ends | February 2027 |
| Registry record updated | November 28, 2025 |
| Trial ID | NCT07092124 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults with low vision who are starting or have begun orthoptic low vision rehabilitation, have binocular visual acuity of at least 1/20 (≤ 1.3 logMAR), can attend at least five rehabilitation sessions before study end, and understand French.
✕Probably not a fit
People with neurodegenerative disease, a history of seizures, significant dominant-upper-limb dysfunction, taking medications that impair motor/visual/cognitive function, pregnant women, or those unable to wear a VR headset or follow study procedures are unlikely to benefit from this test.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The trial uses VisionumVR, a standardized 20-minute virtual reality test delivered on a Meta Quest 3 headset, to probe hand–eye coordination, visual discrimination, and visual exploration through a task inspired by daily activities. Participants who are beginning or already receiving orthoptic low vision rehabilitation will complete the VR test across their rehabilitation course to track change over time. The aim is to determine whether the VR task produces reliable, repeatable measures of functional vision that correlate with rehabilitation progress. Testing excludes people with conditions or medications that could interfere with performance (for example, epilepsy or significant motor impairment).
Why it matters
Potential benefit: If successful, this could give clinicians a quick, standardized, and engaging way to track patients' functional vision and rehabilitation progress.
How similar studies have gone: Small pilot studies and early work suggest VR can help low vision rehabilitation, but standardized, validated VR functional tests like VisionumVR remain limited and are still being tested.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patient (regardless of visual pathology) who is about to begin or has begun orthoptic low vision rehabilitation; * Patient requiring at least five orthoptic rehabilitation sessions that can be completed before the end of the study; * Binocular visual acuity ≥ 1/20 (≤ 1.3 logMAR), regardless of type of vision loss (central, mixed, or peripheral); * Sufficient knowledge of the French language. Exclusion Criteria: * Neurodegenerative diseases or any other condition that could interfere with the planned assessments in this study (known epilepsy and/or history of seizures, dysfunction of the dominant upper limb, etc.); * Medications that may cause motor, visual, or cognitive impairments (neuroleptics, etc.) or interfere with the study assessments; * Pregnant women (pregnancy can cause vision fluctuations, and wearing a virtual reality headset is not recommended); * Participation in another clinical trial that may interfere with the current study; * Inability to follow instructions or read.
Where it's running
-
Centre Régional Basse Vision et Trouble de l'Audition
Angers, France Recruiting -
Institut de Réadaptation Visuelle Saint-Louis
Paris, France Recruiting
Study contacts
- Study coordinator: Amelie Yavchitz, Dr
- Email: ayavchitz@for.paris
- Phone: +33148036454
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.