Clinical trial Recruiting at 1 site Observational Ages 18 to 30

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.

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Quick facts

Study typeObservational
Ages18 Years to 30 Years
SexAll
Enrollment42 (estimated)
SponsorAbant Izzet Baysal University
Academic / other
Locations1 site (Bolu, Bolu)
StatusRecruiting
StartedDecember 15, 2025
Main results expectedDecember 15, 2027
Study endsJanuary 15, 2028
Registry record updatedMay 11, 2026
Trial IDNCT07247773 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

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.