Prospective Pilot Study of Multi-actor Tolerance Evaluation Using the VIRARE Device (VIrtual Reality Assisted Rehabilitation) in Visually Impaired Patients

Centre Hospitalier Universitaire de Nīmes30 enrolled

Overview

Our study aims to validate the relevance of a virtual reality tool (VIRARE: VIrtual REality Assisted Rehabilitation) in the assessment and rehabilitation of visually impaired subjects.

Study Type

INTERVENTIONAL

Allocation

Purpose

OTHER

Masking

NONE

Enrollment

Conditions

Visual Impairment

Interventions

Virtual reality testsDEVICE

The patient will complete 3 self-questionnaires and pass 3 exploratory tests of virtual reality: 1. 10 minutes sitting test: detection of 5 targets in a 360 ° field of vision 2. 10-minute stand-up motionless test: detection of 5 targets in a 360 ° field of view and placing ingredients of a recipe 3. Standing 10-minute test: the patient moves to the site of his mission, detection of 5 targets in a 360 ° field of vision and preparing a recipe

Eligibility

Sex: ALLMin age: 18 YearsMax age: 85 Years

Medical Language ↔ Plain English

Inclusion Criteria: * The patient signed the consent form * The patient is affiliated to a health insurance programme * The patient presents ophthalmological or neurological pathologies with impact on visual function (retinopathy pigmentosa, macular dystrophy, glaucoma, age-related macular degeneration, cerebrovascular accident ...). * The patient is visually impaired (visual acuity less than 3/10 of both eyes or concentric narrowing of the Goldmann binocular visual field or homonymous hemianopia) of category I, II, III or IV of the WHO classification. Exclusion Criteria: * The patient is participating in another study * The patient is in an exclusion period determined by another study * The patient is under safeguard of justice. * The patient is under judicial protection. * It is not possible to give the patient (or his/her trusted-person) informed information. * The patient is pregnant or breastfeeding. * The patient has a sensory or cognitive disability with a given scale (MMS \< 24) * The patient has difficulty moving including major locomotor difficulties.

Locations (1)

Nimes University Hospital

Nîmes, France

Outcomes

Primary Outcomes

dizziness felt by the patient

Yes/no

Time frame: Day 0

Nausea felt by the patient

Yes/no

Time frame: Day 0

headache felt by the patient

Yes/no

Time frame: Day 0

dazzle felt by the patient

Yes/no

Time frame: Day 0

watering of the patient

Yes/no

Time frame: Day 0

eye burns felt by the patient

Yes/no

Time frame: Day 0

Pain due to the mobilization of the eyeballs felt by the patient

Yes/no

Time frame: Day 0

Extraocular pain felt by the patient

Yes/no

Time frame: Day 0

diplopia

Yes/no

Time frame: Day 0

amaurosis

Yes/no

Time frame: Day 0

Fear

Yes/no

Time frame: Day 0

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.