Clinical trial of a take-home rehabilitation device for vestibular patients.
Phase 2
- Conditions
- Reduced vestibulo-ocular reflex response (due to peripheral vestibular dysfunction only).Physical Medicine / Rehabilitation - PhysiotherapyEar - Other ear disorders
- Registration Number
- ACTRN12615000392561
- Lead Sponsor
- euroscience Research Australia
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Stopped early
- Sex
- All
- Target Recruitment
- 21
Inclusion Criteria
Participants must have a well-defined, isolated, peripheral, vestibular lesion, but are otherwise healthy. These lesions could be due to: vestibular neuritis, labyrinthitis, vestibular neurectomy, semicircular canal plugging, superior canal dehiscence and post-intratympanic gentamicin treatment, but not patients with untreated Meniere's disease. Participants can have complete or incomplete unilateral lesions, or incomplete bilateral lesions, i.e., they must have some residual peripheral vestibular function.
Exclusion Criteria
People not fluent in English are unsuitable for these studies and will not be recruited.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method