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Clinical Trials/NCT06213792
NCT06213792
Completed
Not Applicable

Visuo-Vestibular Adaptation in Virtual Reality

Hospices Civils de Lyon1 site in 1 country18 target enrollmentApril 4, 2024
ConditionsHealthy Person

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Healthy Person
Sponsor
Hospices Civils de Lyon
Enrollment
18
Locations
1
Primary Endpoint
VOR gain
Status
Completed
Last Updated
last year

Overview

Brief Summary

The vestibulo-ocular reflex (VOR) stabilizes the gaze during rapid head movements by inducing an eye rotation of equivalent amplitude but in the opposite direction to the head rotation. Normally, the ratio of eye rotation amplitude to head rotation, or VOR gain, is 1. Under some conditions such as growth or the use of corrective glasses, this gain is adapted to the new visuo-vestibular conditions. This well-known sensorimotor adaptation phenomenon can be achieved through the experimental creation of a conflict between vestibular and visual information.

Incremental velocity error (IVE) allows for a rapid adaption of the VOR at high speed by synchronously projecting a laser target that moves to create a progressively increasing visuo-vestibular conflict. However, this method does not correspond to the ecological conditions of VOR use, as the training is conducted in darkness and the visuo-vestibular conflict does not involve the entire visual scene.

Recreating this type of adaptation in a virtual reality environment could allow for adaptation with a visual stimulus involving the entire visual scene, thus more closely resembling the physiological conditions of VOR use. We hypothesize that a visual simulation of the entire scene would be more effective than an isolated target in VOR adaptation during high velocity head rotation.

Registry
clinicaltrials.gov
Start Date
April 4, 2024
End Date
May 2, 2024
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age from 18 to 60
  • Understanding of the experimental instructions
  • Informed Consent

Exclusion Criteria

  • Underlying ENT or neurological disorders
  • Corrected Visual Acuity lower than 5/10
  • Other conditions leading to oscillopsia or ataxia
  • Oculomotor palsy, ocular instability in primary position
  • Treatment that may affect ocular motility (psychotropes)
  • Cervical rachis pathology with instability
  • Cochlear Implants
  • Non-stabilized medical disease
  • Subject suffering from debilitating motion sickness or Virtual Reality sickness
  • Pregnant women

Outcomes

Primary Outcomes

VOR gain

Time Frame: 7 days

VOR gain corresponds to the amplitude of the eye rotation devided by the amplitude of the head rotation for a given head impulse.

Study Sites (1)

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