Validation of Virtual Reality Tests for the Assessment of Patients With Age-related Macular Degeneration as Clinical Endpoints (VIRETTA)

Validation of Virtual Reality Tests for the Assessment of Patients With Age-related Macular Degeneration

Age-related macular degeneration (AMD) is the leading cause of irreversible blindness in industrialized countries and affects tens of millions of people worldwide, with a rapidly increasing prevalence. It causes irreversible central vision loss and significant difficulties in daily activities, impairing patients' quality of life and independence. Conventional clinical assessments, which focus on visual acuity and retinal imaging, do not fully reflect the functional impact of the disease.

Virtual reality (VR) makes it possible to create immersive, controlled environments to accurately measure functional vision and simulate real-life situations. The study proposes to develop a standardized and reproducible functional test in virtual reality that can complement conventional examinations and support clinical and industrial research.

Study Overview

• Status: Not yet recruiting
• Conditions: Geographic Atrophy; Dry AMD; Healhty
• Intervention / Treatment: Other: Object recognition and selection task

• Study Type: Interventional
• Enrollment (Estimated): 60
• Phase: Not Applicable

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: Yes

Description

Inclusion Criteria:

• Age ≥ 50 years
• Sufficient knowledge of the French language
• Ability to give personal, express, free, and informed consent
• Ability to comply with the requirements of the protocol
• Person covered by Social Security
• Clarity of the ocular environment, adequate pupil dilation to allow the collection of good quality images, as determined by the investigator

Additional inclusion criteria for group 1, healthy subjects:

• No detectable visual pathologies
• Best monocular visual acuity ≥ 8/10

Additional inclusion criteria for group 2, subjects with LMA, early AMD, or intermediate AMD without atrophy:

• Diagnosis of AMD, early AMD, or intermediate AMD
• Absence of geographic atrophy
• Presence of drusen (diameter > 63 µm) with or without pigmentary changes

Additional inclusion criteria for group 3, subjects with dry AMD with perifoveal atrophy:

• Diagnosis of atrophic AMD
• Presence of drusen (diameter > 125 µm)
• Location of geographic atrophy as determined by the investigator: extrafoveal, juxtafoveal
• Preservation of central vision confirmed by the investigator based on a comprehensive and integrated interpretation of SD-OCT, FAF, retinography, and best corrected visual acuity examinations.

Additional inclusion criteria for group 4, Subject with dry AMD with foveal atrophy:

• Diagnosis of atrophic AMD
• Presence of drusen (diameter > 125 µm)
• Investigator's localization of geographic atrophy: retrofoveal
• Central vision impairment confirmed by the investigator based on a comprehensive and integrated interpretation of SD-OCT, FAF, retinography, and best corrected visual acuity examinations.

Exclusion Criteria:

• Pregnant women, women in labor, or breastfeeding women
• Subjects undergoing drug treatments that may cause motor, visual, vestibular, or cognitive disorders (PSA, neuroleptics, etc.) or that could interfere with the study examinations
• Any concomitant intraocular condition in the eye being studied (e.g., glaucoma or cataract)
• Any retinal pathology that could cause retinal atrophy other than AMD (eliminate dystrophy, chronic CRSC, pachyatrophy, resorption of vitelliform material with atrophy, high myopia, etc.)
• Known systemic disease that, in the investigator's opinion, would prevent active participation in the study
• Participation in any other therapeutic study evaluating a drug.
• Subjects with cognitive impairment, illiterate subjects, and subjects who do not speak the national language.
• Persons subject to enhanced protection or legal safeguards (guardianship, trusteeship).

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Other
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Main	Other: Object recognition and selection task; The Sight Performance Object Task (SPOT) is a virtual reality (VR) based assessment designed to measure the object recognition and selection capabilities. It functional vision by replicating the real-world challenge of "finding things" under controlled environmental conditions.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of Net selection assessed by the SPOT test	Net selection is the number of selected targets, less the number of selected distractors	Baseline
Number of Net selection assessed by the SPOT test	Net selection is the number of selected targets, less the number of selected distractors	Hour 1
Number of target selection assessed by the SPOT test		Baseline
Number of target selection assessed by the SPOT test		Hour 1

Collaborators and Investigators

• Sponsor: Streetlab
• Collaborators: Fondation Ophtalmologique Adolphe de Rothschild; CIL - Centre Ophtalmologique d'Imagerie et de Laser

Study record dates

Study Major Dates

• Study Start (Estimated): April 1, 2026
• Primary Completion (Estimated): April 1, 2027
• Study Completion (Estimated): April 1, 2027

Study Registration Dates

• First Submitted: February 11, 2026
• First Submitted That Met QC Criteria: February 18, 2026
• First Posted (Actual): February 25, 2026

Study Record Updates

• Last Update Posted (Actual): February 25, 2026
• Last Update Submitted That Met QC Criteria: February 18, 2026
• Last Verified: February 1, 2026

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Eye Diseases; Retinal Diseases; Retinal Degeneration; Macular Degeneration; Geographic Atrophy
• Other Study ID Numbers: 2026-A00272-49

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No