- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04483999
Turkish Validity and Reliability Study of Virtual Reality Sickness Questionnaire
Study Overview
Status
Conditions
Detailed Description
Virtual reality (SG) creates a virtual environment that reflects a real environment and offers various experiences to users. Motion sickness can be observed in people after using virtual reality applications or simulation devices in education. There are questionnaires in the literature such as "Simulator Sickness Questionnaire" and "Motion Sickness Questionnaire". However, these questionnaires are specific surveys to evaluate symptoms that develop after vehicle handling or use of simulation devices for pilot training, while they are not ideal questionnaires to evaluate symptoms that may develop after virtual reality applications. Because there are important differences between virtual reality systems and simulation systems in terms of the appearance of motion disturbance symptoms. For this reason, "Virtual Reality Sickness Questionnaire" has been developed that can evaluate these symptoms.
There is no Turkish version of the "Virtual Reality Sickness Questionnaire" in the literature. For this reason, this study is planned for the cultural adaptation and validity of the "Virtual Reality Sickness Questionnaire".
Study Type
Enrollment (Actual)
Contacts and Locations
Study Contact
- Name: GÜL YAZICIOĞLU
- Phone Number: +903123051577
- Email: fsener@hacettepe.edu.tr
Study Locations
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Sıhhiye
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Ankara, Sıhhiye, Turkey, 06100
- Hatice Çetin
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Not having mental - cognitive problems,
- Being a volunteer
Exclusion Criteria:
- Oculomotor and vestibular disease
- Cardiovascular, neurological and gastrointestinal problems
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Virtual Reality Sickness Questionnaire
Time Frame: Change from Baseline sickness after 1 hour later.
|
This questionnaire assess virtual reality sickness.
This questionnaire consists of 2 subtitles as oculomotor and disorientation.
It contains 9 symptoms in total.
Each symptom is scored between 0 and 3 with the Likert type scoring system.
Each subtitle adapted to be calculated by dividing the total score to a score system in itself like person receives%.
The total score of the questionnaire will be obtained by averaging the total scores of the two subtitles.
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Change from Baseline sickness after 1 hour later.
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graybiel scale
Time Frame: Change from Baseline sickness after 1 hour later.
|
This questionnaire assess virtual reality sickness.
Total score ranges from 0-50.
0-2 points are interpreted as "light susceptibility to motion sickness", 3-7 points as "moderate susceptibility to motion sickness", 8-15 points as "extreme susceptibility to motion sickness", and values above 16 are "Definitive motion sickness".
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Change from Baseline sickness after 1 hour later.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
international physical activity questionnaire
Time Frame: All of the participants will assess at baseline with this scale.
|
This questionnaire assess physical activity level.
The physical activity levels are classified as (< 600 MET-min/week), which is the physically inactive level (level I); (600-3000 METmin/week), which is the level in medium-level (level II) and (> 3000 MET-min/week), which is the high physical activity level.
|
All of the participants will assess at baseline with this scale.
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tampa kinesiophobia scale
Time Frame: All of the participants will assess at baseline with this scale.
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This questionnaire assess kinesiophobia.
The four-point Likert scoring is used in this scale (1 = I do not agree at all, 4 = I agree completely).
The total score is calculated after reversing the items 4, 8, 12 and 16.
Scoring ranges between 17 and 68 with the higher scores indicating higher levels of kinesiophobia perception.
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All of the participants will assess at baseline with this scale.
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Collaborators and Investigators
Sponsor
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- VRSQ9
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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