A study of Vestibular rehabilitation in patients with unilateral vestibular disorder
Not Applicable
- Conditions
- Examination of vestibular rehabilitation for unilateral vestibular vestibular disorder patient
- Registration Number
- JPRN-UMIN000033247
- Lead Sponsor
- Toho University Omori Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
Target patient with general condition and medical history incapable of enforcement of vestibular rehabilitation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method A prospective study Initially, informed consent is executed according to consent explanation document to subjects who wish to participate in this research. If participants wish to undergo rehabilitation at the rehabilitation office, they are classified as an intervention group. If they do not wish to rehabilitate in the rehabilitation office, they are classified as a non-intervention group, and carry out rehabilitation only with rehabilitation guidance by doctors and nurses as before.
- Secondary Outcome Measures
Name Time Method We examine Nystagmus findings, HADS, STAI. With the motor function being secured by Barthel Index, we also evaluate the trajectory length, total area, Short Physical Performance Battery, Functional Gait index, Time up and Go with gravity sway meter. If possible, we'd like to examine maximal slow aspect speed of the nystagmus, CP% of the electronystagmogram(ENG), an amplitude right and left ratio of cVEMP.