Examination of vestibular rehabilitation for unilateral vestibular vestibular disorder patient
Conditions
Interventions
We will examine the items mentioned above at the time of the initial otolaryngology consultation (or at the start of rehabilitation), at the time of discharge (or one week after the start of rehabilit
Sponsors
Toho University Omori Medical Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Unilateral vestibular disorders such as idiopathic hearing loss with vertigo, vestibular neuritisvestibular neuronitis
Exclusion criteria
Exclusion criteria: Target patient with general condition and medical history incapable of enforcement of vestibular rehabilitation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Japan
Contacts
Public ContactOmori Medical Center Ethics Committee
Toho University Omori Medical Center Omori Medical Center Ethics Committee
Outcome results
None listed