Virtual reality stimulation for patients with unilateral vestibular hypofunction
Effect of Optokinetic Virtual Reality Stimulation in Unilateral Vestibular Hypofunction Patients
NA · Istanbul Medipol University Hospital · NCT06517446
This study is testing if virtual reality stimulation can help people with unilateral vestibular hypofunction feel better and improve their balance compared to traditional treatments.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 48 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Istanbul Medipol University Hospital (other) |
| Locations | 1 site (Kocaeli) |
| Trial ID | NCT06517446 on ClinicalTrials.gov |
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.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18-65 diagnosed with unilateral vestibular hypofunction confirmed by a VNG test.
Not a fit: Patients with bilateral vestibular hypofunction, visual impairments, neurological disorders, or communication difficulties may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance rehabilitation outcomes for patients suffering from unilateral vestibular hypofunction.
How similar studies have performed: While the use of virtual reality in vestibular rehabilitation is emerging, this specific approach has not been widely tested, making it a novel investigation.
Eligibility criteria
Show full inclusion / exclusion criteria
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 this trial is running
Kocaeli
- Kocaeli Health and Technology University — Kocaeli, Turkey (Türkiye) (RECRUITING)
Study contacts
- Study coordinator: Ebru SEVER, Doktora, PT
- Email: fztebrusever@gmail.com
- Phone: 05336824227
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Vestibular Hypofunction, Unilateral Vestibular Hypofunction, Virtual Reality, Optokinetic stimulation, Motion Sickness