Turkish adaptation of the Cybersickness in Virtual Reality Questionnaire (CSQ-VR)
Official title: Turkish Validity and Reliability of CyberSickness in Virtual Reality Questionnaire
Run by Abant Izzet Baysal University · NCT07247773 · Data updated 2026-11-12
This project tests whether a Turkish version of the CSQ-VR questionnaire reliably measures cybersickness symptoms in healthy volunteers who use virtual reality.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 30 Years |
| Sex | All |
| Enrollment | 42 (estimated) |
| Sponsor | Abant Izzet Baysal University Academic / other |
| Locations | 1 site (Bolu, Bolu) |
| Status | Recruiting |
| Started | December 15, 2025 |
| Main results expected | December 15, 2027 |
| Study ends | January 15, 2028 |
| Registry record updated | May 11, 2026 |
| Trial ID | NCT07247773 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal participants are healthy adults who can stand and walk independently, have normal binocular 3D vision, and consent to testing including the Titmus stereotest.
✕Probably not a fit
People with amblyopia, strabismus, other vision pathologies that impair depth perception, or who cannot attend the on-site assessments are unlikely to benefit directly from this validation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The study adapts the CSQ-VR into Turkish and recruits healthy volunteers at Abant Izzet Baysal University to complete the questionnaire after VR exposure. Participants are screened for normal binocular 3D vision and must be able to stand and walk independently, with those failing the Titmus stereotest excluded. Data will be analyzed for reliability (e.g., internal consistency, test-retest) and validity (e.g., construct and convergent validity) to determine whether the Turkish CSQ-VR measures cybersickness consistently and accurately. The study situates the instrument within existing theories of cybersickness such as sensory conflict and vection as background for interpretation.
Why it matters
Potential benefit: If successful, the Turkish CSQ-VR could give researchers and VR developers a reliable tool to identify and reduce cybersickness in Turkish-speaking users.
How similar studies have gone: Similar questionnaire adaptation and validation studies for cybersickness and simulator sickness have been conducted successfully in other languages, though a Turkish CSQ-VR is novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Voluntary agreement to participate in the study * Ability to stand and walk independently Exclusion Criteria: * Presence of amblyopia, strabismus, or pathologies impairing focus, depth perception, or normal 3D vision * Failure on the butterfly test of the Titmus stereotest
Where it's running
-
Abant Izzet Baysal University Faculty of Health Science
Bolu, Bolu, Turkey (Türkiye) Recruiting
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.