Reliability and Validity of the French Version of the Virtual Reality Sickness Questionnaire (VRSQ-F)

Pôle Saint Hélier

Status: Completed

Conditions: Virtual Reality Cyber Sickness

Treatments: Diagnostic Test: Use of Measurement Instrument

Study type: Interventional

Funder types: Other

Identifiers

NCT06466590

2023-A02468-37

Details and patient eligibility

About

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.

Enrollment: 88 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

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)

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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88 participants in 1 patient group

Single Group

Experimental group

Description:

Participants will be asked to use the measurement instrument VRSQ-F on two separate occasions under identical conditions to assess its test-retest reliability and asked to use the SSQ for validity. Each session will involve completing the measurement protocol as specified.

Treatment:

Diagnostic Test: Use of Measurement Instrument