Turkish Validity and Reliability of VRSUQ
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Healthy Volunteer. Basic parameters: 18 years — 50 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Turkish Validity and Reliability of Virtual Reality System Usability Questionnaire
Overview
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.
Detailed description
Virtual reality-based rehabilitation approaches are attracting increasing attention and research. It is a necessity and a challenge for researchers to demonstrate the degree of usability of existing or newly designed applications suitable for rehabilitation purposes. For this purpose, the System Usability Scale designed to evaluate the usability of simulations is used, but it does not contain items specifically for immersive virtual reality. The usability scale developed specifically for immersive virtual reality aims to fill this gap. This study was planned to conduct a Turkish validity and reliability study of this questionnaire.
Primary outcome measures
- Virtual Reality System Usability Questionnaire [Time frame: From enrollment to the second assesment at 2 weeks]
Eligibility criteria
Inclusion criteria
- Accepting to participate in the research
- To be between the ages of 18-50
- Ability to stand and walk independently
Exclusion criteria
- 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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Other
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07247747 · AIBU-FTR-BENLI-007