Turkish Adaptation of the CSQ-VR

NCT07247773 | Not Yet Recruiting

• 1 other identifier: AIBU-FTR-BENLI-008
• Study Type: observational
• Target: 42
• Locations: 1 country
• Sites: 1

Brief Summary

The Cybersickness in Virtual Reality Questionnaire (CSQ-VR) is a tool designed to measure the presence and intensity of cybersickness symptoms experienced in VR. The CSQ-VR is an adapted and improved version of the Cybersickness section of the Virtual Reality Neuroscience Questionnaire (VRNQ). The aim of this study is to examine the validity and reliability of the Turkish version of the CSQ-VR.

Conditions

Healthy Volunteers

Keywords

Virtual Reality; Cybersickness

Outcome Measures

Primary Outcomes (1)

• Cybersickness in Virtual Reality Questionnaire

  It is a tool designed to measure the presence and severity of cybersickness symptoms experienced in VR

  Immediately after a single VR session (~1 hour)

Secondary Outcomes (1)

• Simulator Sickness Questionnaire

  Immediately after a single VR session (~1 hour)

Study Arms (1)

Healthy volunteer

A group of healthy participants will rate the symptoms induced in virtual reality using questionnaire items.

Eligibility Criteria

• Age: 18 Years - 30 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)
• Sampling Method: Non-Probability Sample

Study Population

Healthy volunteers aged 18-30 years with independent standing and walking ability will be recruited.

You may qualify if:

• Voluntary agreement to participate in the study
• Ability to stand and walk independently

You may not qualify if:

• Presence of amblyopia, strabismus, or pathologies impairing focus, depth perception, or normal 3D vision
• Failure on the butterfly test of the Titmus stereotest

Sponsors & Collaborators

• Abant Izzet Baysal University: lead

Study Sites (1)

Abant Izzet Baysal University Faculty of Health Science

Bolu, Bolu, 14100, Turkey (Türkiye)

Location

Study Design

• Study Type: observational
• Observational Model: OTHER
• Time Perspective: PROSPECTIVE
• Target Duration: 1 Day
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Assistant Professor

Study Record Dates

• First Submitted: November 18, 2025
• First Posted: November 25, 2025
• Study Start: December 15, 2025
• Primary Completion (Estimated): December 15, 2027
• Study Completion (Estimated): January 15, 2028
• Last Updated: November 25, 2025

Record last verified: 2025-10

Data Sharing

• IPD Sharing: Will not share

Locations

TU (1)