Activity Treatment on Vestibular Rehabilitation

Vestibular Disorder Clinical Trial

Official title:

Comparison of Activity-Based Home Program and Cawthorne-Cooksey Exercises in Patients With Chronic Unilateral Peripheral Vestibular Disorders

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04425928
• Other study ID #: 5057087198
• Status: Completed
• Phase: N/A
• Start date: April 15, 2018
• Est. completion date: November 19, 2019

Study information

• Verified date: August 2020
• Source: Gazi University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

In this study it was aimed to investigate the effects of home treatment program based standard activity on dizziness, balance and daily life activity in patients with dizziness complaint originated from chronic unilateral peripheral vestibular disorder and compare to effects of exercise-based home rehabilitation program.

Description:

The aim of this study was to assess the effects of an activity training programme on dizziness, imbalance, and level of independence in daily living activities in patients with chronic dizziness. 75 patients between 18-65 years of age who diagnosed chronic peripheral vestibular disorders and individuals with vestibular rehabilitation indications were included in our study. Patients were randomly divided into 3 groups consist of 25 patients as an activity group, exercise group, and control group. Education was given to each group. İn addition, the activity group was performed a training activities program, the exercise group was performed in the Cawthorne-Cooksey exercises program. Therapy programs were prescribed once daily at home for 4 weeks. After demographic information was obtained from all patients, assessments were performed at the beginning and at the end of the treatment program (4 weeks). Dizziness severity was assessed by the Visual Analog Scale (VAS), activities of daily livings were assessed by Vestibular Disorders Activity Questionnaire (VADL) and balance was assessed by Sensory Organization Testing (SOT).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 75
• Est. completion date: November 19, 2019
• Est. primary completion date: June 1, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 64 Years

Eligibility

Inclusion Criteria:

• Patients have dizziness complaint longer than 3 months,

• History of at least one dizziness in a month

• Patient has been diagnosed chronic unilateral peripheric vestibular disorder

Exclusion Criteria:

• Patients with diagnosed benign paroxysmal positional vertigo, had Meniere's disease, had history of central nerve system impairments and/or psychiatric disorder, had uncontrolled hypertension and diabetes, had not understanding simple verbal instruction and following ability, not able to stand independent in the standstill position, had visual problems that cannot be treated with lenses or glasses, had movement limitation due to the orthopedic problem, using medication for dizziness.

Related Conditions & MeSH terms

• Ear Diseases
• Vestibular Diseases
• Vestibular Disorder

Intervention

Procedure:
• occupational therapy based activity training programs
Occupational therapy based activity training programs in which exercises based on physiotherapy are put into the purposeful activities at vestibular rehabilitation.
• Physiotherapy based exercise training programs
Cawthorne-cooksey exercises were performed at vestibular rehabilitation

Locations

Country	Name	City	State
Turkey	Hacettepe University	Ankara

Sponsors (1)

Lead Sponsor	Collaborator
Bilgehan Tekin Dal

Country where clinical trial is conducted

Turkey, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Change from before and after treatment in the postural stability on Computerized Dynamic Posturography (CDP).	Computerized dynamic posturography (CDP) testing is a technique used to assess underlying sensory and motor control impairments associated with balance disorders.	before and after treatment (4 weeks)
Primary	Change from before and after treatment in the severity of dizziness on Visual Analog scale (VAS).	VAS is a self-reported instrument assessing the severity of diziness.	before and after treatment (4 weeks)
Secondary	Change from before and after treatment in the Independent level of activity in the daily life on Vestibular Disorders Activities of Daily Living Scale (VADL).	VADL is a questionnaire assessing the Independent level of activity in daily life.	before and after treatment (4 weeks)