An interventional study of physiotherapy in Motion Sickness, sponsored by University Hospital, Caen. Status unknown at 2 sites in France. Open to participants aged 18 Years to 67 Years. Per ClinicalTrials.gov, last updated 2022-11-28.
Sponsored by University Hospital, Caen · Not applicable, Interventional, and Treatment
Evaluation of a virtual reality desensitization protocol on subjects with severe motion sickness and study of the role of the emotional component on the effectiveness of the therapy.
Motion sickness is a well-known syndrome, particularly at risk in children, with a maximum around the age of 12. All people are sensitive to motion sickness in childhood, probably related to the maturation of certain cognitive functions of a spatial nature, namely the perception of oneself and one's movements in one's environment. These symptoms regress with age for a part of the population but a large number of people will remain sensitive to certain conditions of displacement and generate symptoms that can be extremely disabling and handicapping in everyday life, particularly for professional activities. For example, some people can no longer use their car, some can no longer take the boat for professional activities in restrictive and/or extreme environments (sailors, scientists, workers, etc.). Behavioral, respiratory or medicinal therapies remain partially effective due to the lack of sufficient knowledge on the physiopathology of this syndrome classified in the field of sensory disorders. Very recently, techniques of sensory desensitization by visual stimulation have appeared, either optokinetic or in virtual reality mimicking the environment that causes this syndrome. This therapeutic approach seems to give empirically good results but only one study has shown it with optokinetic stimulation but it is to be evaluated for virtual reality.
The main objective of the study is therefore to evaluate the effectiveness of a sensory conflict protocol generated in virtual reality to reduce the severity of motion sickness. Each subject being his own control. An observational study was then designed to quantify the effectiveness of this technique carried out in a current way by the physiotherapists in the form of questionnaires supplemented by a posturographic evaluation of the sensory profile of the subjects. If the effectiveness is proven, this desensitization protocol could be optimized and more widely distributed. Furthermore, the analysis of the visuo-dependence variable (from the sensory profile) will indicate whether the use of a visual stimulus by virtual reality alone is sufficient or should be combined or compared with desensitization of other sensory modalities. The use of galvanic vestibular stimulation for the rehabilitation of vestibular pathologies or training programs based on the resolution of sensory conflicts could be envisaged in the future.
50 studies on the registry are indexed under Motion Sickness; 9 are open to participants now.
This study's planned enrollment of 30 is below the median of 59 across 44 interventional studies indexed under Motion Sickness.
Browse Motion Sickness studies →University Hospital, Caen is the lead sponsor of 512 studies on the registry; 82 are open to participants now.
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Exclusion Criteria:
one group of patient
Other: physiotherapy
rehabilitation through using session of virtual reality desensitization
motion sickness severity
simulator sickness questionnaire (0-64)
Time frame: day 0 (day before the first session of rehabilitation)
motion sickness severity
simulator sickness questionnaire (0-64)
Time frame: day 30 (day after the end of rehabilitation)
Emotion
The State-Trait Anxiety Questionnaire (0-80)
Time frame: day 0 (day before the first session of rehabilitation)
Emotion
The State-Trait Anxiety Questionnaire (0-80)
Time frame: day 30 (day after the end of rehabilitation)
Posture
postural measurement (gravity center ellipse)
Time frame: day 0 (day before the first session of rehabilitation)
Posture
postural measurement (gravity center ellipse)
Time frame: day 30 (day after the end of rehabilitation)
Plan to share: No
This study is status unknown, as verified in Aug 2022. You cannot join it, but the record below documents what was studied.
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