Actively Recruiting
Optokinetic Virtual Reality Stimulation in Unilateral Vestibular Hypofunction
Led by Istanbul Medipol University Hospital · Updated on 2026-03-04
48
Participants Needed
1
Research Sites
34 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The study will be conducted on patients diagnosed with UVH who apply to Prof. Dr. Mete İşeri Ear, Nose and Throat Diseases Polyclinic and Güneşli Erdem Hospital Ear, Nose and Throat and Vestibular Rehabilitation Unit. Participants will be divided into 3 groups by simple randomization (closed envelope) method. To the vestibular rehabilitation group; A conventional rehabilitation program based on structured Cawthorne Cooksey exercises will be applied for 45 minutes once a week with the support of a physiotherapist for 8 weeks. To the optokinetic stimulation group; optokinetic stimulation will be given with virtual reality glasses, and to the combined group; Participants in the vestibular exercise group will receive additional optokinetic stimulation. The application will be done once a week for 8 weeks. Inclusion criteria for the study are; diagnosed with unilateral vestibular hypofunction with VNG test, between the ages of 18-65, class A+ in the System Usability Scale (SUS) and the percentage range being between 96-100%; Exclusion criteria for the study are; Bilateral vestibular hypofunction, visual impairment, neurological disorder and inability to communicate.
CONDITIONS
Official Title
Optokinetic Virtual Reality Stimulation in Unilateral Vestibular Hypofunction
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosed with unilateral vestibular hypofunction confirmed by VNG test
- Between 18 and 65 years old
- System Usability Scale (SUS) A+ class with percentile between 96 and 100
You will not qualify if you...
- Bilateral vestibular hypofunction
- Visual impairment
- Neurological disorder
- Inability to communicate
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Kocaeli Health and Technology University
Kocaeli, Turkey (Türkiye), 41000
Actively Recruiting
Research Team
E
Ebru SEVER, Doktora, PT
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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