Virtual reality stimulation for patients with unilateral vestibular hypofunction

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates the effects of optokinetic virtual reality stimulation on patients diagnosed with unilateral vestibular hypofunction (UVH). Participants will be randomly assigned to one of three groups: a conventional vestibular rehabilitation group, an optokinetic stimulation group using virtual reality glasses, or a combined group receiving both interventions. Each group will undergo their respective treatments once a week for eight weeks, with the aim of improving vestibular function and reducing symptoms. The study will assess the efficacy of these interventions through various measures, including patient usability and symptom relief.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Diagnosed with unilateral vestibular hypofunction with VNG test,
* Being between the ages of 18-65,
* Being in the A+ class on the System Usability Scale (SCS) and having a value between 96-100 percentile

Exclusion Criteria:

* Having bilateral vestibular hypofunction
* Having a visual impairment,
* Having a neurological disorder
* Inability to communicate

Where it's running

• Kocaeli Health and Technology University
  Kocaeli, Turkey (Türkiye) Recruiting

Study contacts

• Study coordinator: Ebru SEVER, Doktora, PT
• Email: fztebrusever@gmail.com
• Phone: 05336824227

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.