Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT06517446

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

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

You will not qualify if you...

  • Bilateral vestibular hypofunction
  • Visual impairment
  • Neurological disorder
  • Inability to communicate

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Kocaeli Health and Technology University

Kocaeli, Turkey (Türkiye), 41000

Actively Recruiting

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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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