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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT02746770
Other study ID # vestibularuja
Secondary ID
Status Active, not recruiting
Phase N/A
First received February 25, 2016
Last updated April 20, 2016
Start date February 2016
Est. completion date April 2016

Study information

Verified date April 2016
Source University of Jaén
Contact n/a
Is FDA regulated No
Health authority Spain: Ethics Committee
Study type Interventional

Clinical Trial Summary

Spanish population with unilateral peripheral vestibular disorders.


Description:

Participants with peripheral vestibular disorders will be allocated to a Cawthorne and Cooksey exercises protocol or control group. The Cawthorne and Cooksey exercises consist in some head mobilization and positioning tasks which are related with a restoration of vestibular disorders.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 80
Est. completion date April 2016
Est. primary completion date April 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Participants with with unilateral peripheral vestibular disorders

Exclusion Criteria:

- Bilateral vestibular disorders

- Fluctuating or active unilateral vestibular disease

- Or other medical conditions in the acute phase were excluded from the study.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Experimental: Cawthorne and Cooksey exercises group
Experimental: intervention group. Patients assigned to the experimental group will perform the Cawthorne and Cooksey exercises for vestibular rehabilitation in addition to their habitual treatment.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Jaén

Outcome

Type Measure Description Time frame Safety issue
Primary Activities-specific Balance Confidence scale (ABC) Activities-specific Balance Confidence scale (ABC), to quantify the level of confidence in performing a specific task without losing balance or becoming unsteady. This scale is applied to assess the change due to intervention between the baseline and 6 weeks of treatment. So the data will be collected at baseline and after 6 weeks of treatment. Baseline and after 6 weeks of intervention No
Secondary UCLA Dizziness Questionnaire (UCLA-DQ) UCLA Dizziness Questionnaire (UCLA-DQ), used to measure the severity and frequency of dizziness and its impact on quality of life. This questionnaire is applied to assess the change due to intervention between the baseline and 6 weeks of treatment. So the data will be collected at baseline and after 6 weeks of treatment. Baseline and after 6 weeks of intervention No
Secondary Dizziness Handicap Inventory (DHI), Dizziness Handicap Inventory (DHI), to assess the level of disability and handicap.This questionnaire is applied to assess the change due to intervention between the baseline and 6 weeks of treatment. So the data will be collected at baseline and after 6 weeks of treatment. Baseline and after 6 weeks of intervention No
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