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Validation of a Virtual Reality Test for the Assessment of Visually Impaired Patients Undergoing Low Vision Rehabilitation

Validation of a Virtual Reality Test for the Assessment of Visually Impaired Patients Undergoing Low Vision Rehabilitation

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07092124
Acronym
VisionumVR
Enrollment
60
Registered
2025-07-29
Start date
2025-10-30
Completion date
2027-02-28
Last updated
2025-11-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low Vision

Brief summary

Low vision rehabilitation is a vital part of care for visually impaired patients, who are usually referred to orthoptists to develop visual strategies and optimize residual vision. This rehabilitation significantly improves quality of life by enhancing autonomy and reducing depression. It employs various tools, from traditional exercises to specialized software. Advances in virtual reality (VR) offer new promising opportunities by creating immersive environments tailored to patients' residual vision, increasing motivation and exercise effectiveness. In this context, VisionumVR was developed-a VR test using the Meta Quest 3 headset to assess functional vision during rehabilitation. It evaluates hand-eye coordination, visual discrimination, and visual exploration through a daily-life-inspired task. This standardized 20-minute test aims to measure patients' progress throughout their orthoptic rehabilitation.

Interventions

DEVICEtest visionumVR

Two evaluation sessions with VisionumVR one month apart

Sponsors

Streetlab
CollaboratorINDUSTRY
Fondation Ophtalmologique Adolphe de Rothschild
Lead SponsorNETWORK

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
repetabilityDay 0 and Month 1Repeatability coefficient of performance on the VisionumVR test

Countries

France

Contacts

Primary ContactAmelie Yavchitz, Dr
ayavchitz@for.paris+33148036454

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026