Skip to main content
Clinical Trials/NCT03973255
NCT03973255
Completed
N/A

Efficacy Of Biofeedback Training And Whole Body Vibration Therapy In Vestibular Rehabilitation Of Unilateral Vestibular Weakness

Pamukkale University1 site in 1 country90 target enrollmentMarch 13, 2018

Overview

Phase
N/A
Intervention
Not specified
Conditions
Vestibular Disease
Sponsor
Pamukkale University
Enrollment
90
Locations
1
Primary Endpoint
vertigo visual analogue scale
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The aim of this study was to compare the efficacy of home based vestibular rehabilitation program, posturographic biofeedback training and whole body vibration therapy on balance, fall risk, functional mobility, vertigo symptom severity and functions in patients with unilateral vestibular weakness.

Detailed Description

A total of 90 patients who were diagnosed as unilateral vestibular weakness were included in this prospective randomized controlled study. They were randomized into three groups each consisting of 30 patients. Home based vestibular rehabilitation program was given to all groups. Fall risk yielded by posturography, Berg balance scale, Timed Up-and-Go test, vertigo visual analogue scale and Dizziness Handicap Inventory were used for comparison.

Registry
clinicaltrials.gov
Start Date
March 13, 2018
End Date
March 31, 2019
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Fazıl Necdet Ardıç

Prof.Dr.Fazıl Necdet Ardıç

Pamukkale University

Eligibility Criteria

Inclusion Criteria

  • Adult patients who had unilateral vestibular weakness and persistent dizziness at least two months after acute period were included Bithermal caloric test showing hyporesponsiveness higher than 30% or unresponsiveness of the horizontal canal of the affected ear accepted as unilateral vestibular weakness.

Exclusion Criteria

  • Bilateral vestibular weakness, Recurrent vestibulopathy, Benign paroxysmal positional vertigo, Concomitant neurological or psychiatric disease, Severe visual or auditory impairments and orthopedic problems in the lower extremities

Outcomes

Primary Outcomes

vertigo visual analogue scale

Time Frame: 30 days

A vertically oriented 10 cm line was used for VAS, where "no vertigo" corresponds to the bottom of the line and "the worst vertigo that they could imagine" corresponds to the top of the line. Patients were instructed to place a mark on the 10-cm vertical line according to severity of their vertigo.

Dizziness Handicap Inventory

Time Frame: 30 days

The DHI has 25 items, sub-grouped into three domains: functional, emotional, and physical. There are three closed-form answers where patients may check one of the following: yes, sometimes and no with the corresponding scored as 4/2/0. It is possible to use both the total score and the scores of the three subscales separately.

fall risk

Time Frame: 30 days

fall risk yielded by static posturography

Timed Up-and-Go

Time Frame: 30 days

TUG is a balance and gait index which requires subjects to rise from an armchair, walk 3 m at a normal and safe pace, turn around, walk back to the chair and sit-down. The time required to complete this task is measured in seconds.

Berg balance scale

Time Frame: 30 days

BBS consists of 14 tasks that are each scored on a scale of 0-4, for a total possible score of 56, indicating no identified balance difficulties. Scoring is on a 5-point ordinal scale with 0 indicating an inability to complete the task and 4 as independent in completing the task.

Study Sites (1)

Loading locations...

Similar Trials