Clinical Trials Logo

Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06213792
Study type Observational
Source Hospices Civils de Lyon
Contact
Status Completed
Phase
Start date April 4, 2024
Completion date May 2, 2024

See also
  Status Clinical Trial Phase
Recruiting NCT06432738 - ZL-82 Double-blind Clinical Trial Phase 1
Recruiting NCT05693233 - Effect of Soft Robotic Exosuit Assistance in Healthy People N/A
Completed NCT01745835 - Comparison Between 2L Coolprep® and Combination of 1L Coolprep® and Bisacodyl as Bowel Preparation Phase 3
Terminated NCT03775473 - PROgastrine COlon DEpistage N/A
Recruiting NCT06387966 - A Randomized, Double-blind,Dose-escalating, Single-dose, Oral Phase I Clinical Study of Flunotinib Healthy People Phase 1
Completed NCT05316857 - DDI Study of Orelabrutinib Phase 1