Turkish Validity and Reliability of VRSUQ

NCT07247747 | Not Yet Recruiting

• 1 other identifier: AIBU-FTR-BENLI-007
• Study Type: observational
• Target: 54
• Locations: 0 countries
• Sites: N/A

Brief Summary

The aim of this study is to conduct a Turkish validity and reliability study of the Virtual Reality System Usability Questionnaire (VRSUQ), which can evaluate virtual reality from various aspects by taking into account the characteristics of virtual reality and usability evaluation indicators.

Conditions

Healthy Volunteer

Outcome Measures

Primary Outcomes (1)

• Virtual Reality System Usability Questionnaire

  The Virtual Reality System Usability Questionnaire consists of usability evaluation indicators that reflect the characteristics of VR applications and the questionnaire consists of nine items. The Virtual Reality System Usability Questionnaire includes questions about the response time of the system, clarity of feedback and ease of error correction specific to VR systems. 9 items scored on a five-point Likert scale (1 = strongly disagree, 5 = strongly agree). Negative-worded items are reverse-coded. Final scores are converted to a 0-100 scale, with higher scores indicating better perceived usability.

  From enrollment to the second assesment at 2 weeks

Study Arms (1)

Virtual reality group

They will experience some virtual reality applications and carry out questionnaires to test the validity and reliability of the scale

Eligibility Criteria

• Age: 18 Years - 50 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)
• Sampling Method: Non-Probability Sample

Study Population

Bolu Abant Izzet Baysal University Faculty of Health Sciences will be held with the participation of students and academicians

You may qualify if:

• Accepting to participate in the research
• To be between the ages of 18-50
• Ability to stand and walk independently

You may not qualify if:

• Scores below 24 on the mini mental test
• Scoring 10 and above on the simulator disease questionnaire
• People with amblyopia, strabismus and pathologies that interfere with focusing, depth perception or normal 3D vision
• Failure of the fly test in the Titmus test

Sponsors & Collaborators

• Abant Izzet Baysal University: lead

Central Study Contacts

Enes T Benli, Ph.D

CONTACT

+90 (0374) 254 10 00; enestayyipbenli@gmail.com

Study Design

• Study Type: observational
• Observational Model: OTHER
• Time Perspective: PROSPECTIVE
• Target Duration: 1 Week
• 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 1, 2026
• Study Completion (Estimated): June 15, 2027
• Last Updated: December 2, 2025

Record last verified: 2025-03