Virtual Reality Cyber Sickness
Conditions
Keywords
virtual reality, cyber sickness, assessment
Brief summary
This is a multicenter, controlled, non-randomized interventional clinical study, with minimal risks and constraints, aimed at verifying the reliability of the French version of the VRSQ questionnaire (VRSQ-F) and the validity of the VRSQ-F score by comparing it with the SSQ score.
Interventions
DIAGNOSTIC_TESTUse of Measurement Instrument
Participants will complete the measurement procedure twice, with sessions scheduled one week apart, using the same instrument under standardized conditions. The results from both sessions will be compared to assess the instrument's consistency and accuracy
Sponsors
Pôle Saint Hélier
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE
Intervention model description
All participants will perform 4 exercises in virtual reality with HMD (Head Mounted Display). Then, they will use the VRSQ-F instrument under study on 2 times separated by 15 minutes. The primary objective is to assess the reliability and validity of this instrument through repeated measures and comparison to SSQ
Eligibility
Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes
Inclusion criteria
For Healthy people : * Men or women aged 18 to 65 * Person affiliated to a social security scheme * Healthy person with no particular medical condition * Having given their consent to participate in the research For patients : * Men or women aged 18 to 65 * Persons affiliated to a social security scheme * People undergoing regular rehabilitation, walking or in a wheelchair, who can use a virtual reality solution as part of their care. * Having given their consent to take part in the research
Exclusion criteria
* Vestibular and cardiac pathologies, and major visual disorders not compatible with virtual reality rehabilitation * Cognitive and language disorders * Persons under legal protection * Pregnant women * MSSQ greater than 15 * People suffering from photosensitive epilepsy * Persons under the influence of medication that may impair drugs or alcohol * Participant with an implanted medical device that may be affected by radio waves emitted by compatible third-party equipment (e.g. : Pacemaker)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Check the validity of the VRSQ-F score by comparing it with the SSQ score | Immediately after exercises | Criteria validity between SSQ and VRSQ-F. SSQ questionnaire with 16 questions scoring from 0 to 48 VRSQ-F questionnaire with 9 questions from 0 to 27 |
| Reliability of VRSQ-F (Virtual Reality Sickness Questionnaire) using the intraclass correlation coefficient between measurements immediately after VR exercises and 15 min after and Cronbach coefficient of the VRSQ-F questionnaire | Immediately after exercises | Reliability of VRSQ-F (Virtual Reality Sickness Questionnaire) using the intraclass correlation coefficient between measurements immediately after VR exercises and 15 min after and Cronbach coefficient of the VRSQ-F questionnaire |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Calculate the minimum detectable change in the questionnaire | Immediately after exercises | Clinimetric quality: Calculation of the standard error of measurement SEM and the minimum detectable change MDC |
Countries
France
Outcome results
None listed