Healthy VolunteerNCT07247747
Turkish Validity and Reliability of VRSUQ
An observational study of Healthy Volunteer, run by Abant Izzet Baysal University at 1 site in Turkey (Türkiye).
Trial 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. Read more about this study
- Who is it for?
- Ages 18 to 50 yearsHealthy volunteers can take part
- Conditions the study is for
- Healthy Volunteer
- How many people
- 70 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 15 Oct 2025to 15 Jun 2026
- How long will I take part?
- 1 Week
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 50 years
- All sexes
- Healthy volunteers accepted
- Adult
Study population: Bolu Abant Izzet Baysal University Faculty of Health Sciences will be held with the participation of students and academicians
Who may be able to join
- Accepting to participate in the research
- To be between the ages of 18-50
- Ability to stand and walk independently
Who cannot join
- 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
Trial locations and contacts
1 site in 1 country.
Turkey (Türkiye)1 site
Abant Izzet Baysal University Faculty of Health Science
Bolu, Bolu, 14100
About this study
Official title: Turkish Validity and Reliability of Virtual Reality System Usability Questionnaire
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.
Read the 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.
- Conditions
- Healthy Volunteer
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Virtual reality group | They will experience some virtual reality applications and carry out questionnaires to test the validity and reliability of the scale |
What is being measured
The primary outcome is the main question the study is designed to answer.
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.
Measured: From enrollment to the second assesment at 2 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted25 Nov 2025
- Study start15 Oct 2025
- Primary completion15 Jan 2026
- Study completion15 Jun 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Healthy VolunteerStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Other
- Time perspective
- Prospective
- Enrolment
- 70 participants (actual)
- Target duration
- 1 Week
Sponsor and investigators
- Lead sponsor
- Abant Izzet Baysal University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, enes tayyip benli, Abant Izzet Baysal University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07247747
- Sponsor's protocol ID
- AIBU-FTR-BENLI-007
- Status last verified
- Mar 2025
- First submitted
- 18 Nov 2025
- Last updated
- 29 Oct 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 29 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Turkish Validity and Reliability of Virtual Reality System Usability Questionnaire
- ClinicalTrials.gov ID
- NCT07247747
- Acronym / sponsor ID
- AIBU-FTR-BENLI-007
- Conditions
- Healthy Volunteer
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 70 participants (actual)
- Lead sponsor
- Abant Izzet Baysal UniversityUniversity, hospital or other
- Study start
- 15 Oct 2025 (actual)
- Primary completion
- 15 Jan 2026 (actual)
- Study completion
- 15 Jun 2026 (actual)
- First posted
- 25 Nov 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Study design
- Observational model
- Other
- Time perspective
- Prospective
- Target follow-up
- 1 Week
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Virtual reality group | – | –They will experience some virtual reality applications and carry out questionnaires to test the validity and reliability of the scale |
Who may qualify
- Ages
- 18 to 50 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
- Study population
- Bolu Abant Izzet Baysal University Faculty of Health Sciences will be held with the participation of students and academicians
Key inclusion criteria (3 listed)
- Accepting to participate in the research
- To be between the ages of 18-50
- Ability to stand and walk independently
Key exclusion criteria (4 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Virtual Reality System Usability Questionnaire
Time frame: From enrollment to the second assesment at 2 weeks
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.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 29 Oct 2026.
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Irritability
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Healthy Volunteer, run by Abant Izzet Baysal University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 29 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Virtual Reality System Usability Questionnaire (time frame: From enrollment to the second assesment at 2 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 29 Oct 2026.