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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03952936
Other study ID # 5/14/2020 CVD
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 1, 2018
Est. completion date August 30, 2019

Study information

Verified date October 2023
Source Methodist University, North Carolina
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to assess the effectiveness of vestibular rehabilitation for an individual who has chronic central vestibular deficits due to cerebellar dysfunction. Due to the lack of treatment for chronic cerebellar dysfunction with Physical Therapy, the investigators hope to produce a protocol for chronic cerebellar dysfunction utilizing balance training, vestibular rehabilitation, or any other rehabilitation technique that may alleviate or eliminate symptoms.


Description:

The purpose of this study is to assess the effectiveness of vestibular rehabilitation for an individual who has chronic central vestibular deficits due to cerebellar dysfunction. Due to the lack of treatment for chronic cerebellar dysfunction with Physical Therapy, the investigators hope to produce a protocol for chronic cerebellar dysfunction utilizing balance training, vestibular rehabilitation, or any other rehabilitation technique that may alleviate or eliminate symptoms. Investigators will test the subject initially at 4 weeks, 8 weeks and 6 months post start date to assess for symptom improvement.


Recruitment information / eligibility

Status Completed
Enrollment 1
Est. completion date August 30, 2019
Est. primary completion date August 30, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group N/A and older
Eligibility Inclusion Criteria: - Central vestibular deficits Exclusion Criteria: - None

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Vestibular Rehabilitation
standard vestibular rehabilitation with gaze stability, balance training, habituation tailored to the subject

Locations

Country Name City State
United States Methodist Universtiy Fayetteville North Carolina

Sponsors (1)

Lead Sponsor Collaborator
Methodist University, North Carolina

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Activity Specific Balance Confidence Scale Perceived self confidence with balance. 16 items are scored on a 0-100% scale. Items are totaled and then averaged. The higher the average score the higher the confidence with balance and the less likely risk there is for falling. 2-6 months
Secondary Dizziness handicap inventory Perceived handicap from dizziness. Items are scored on a 0, 2 or 4 point scale with adding up the total number of the 26 items. The lower the score, the less perceived amount of handicap is present. 2-6 months
Secondary Functional Gait Assessment Gait and balance test. 10 item test rated on each item from 0-3. total score is calculated of 10 items. the higher the score the less likely risk for falling is present. 2-6 months
Secondary Motion Sensitivity Quotient Motion sickness indicator. 16 items are scored based on symptom severity and duration. positive items are calculated together to receive a percentage. the lower the percentage the less motion sensitivity a person has. 2-6 months
Secondary Modified Clinical Test for Sensory Integration in Balance balance test for sensory system inputs. 6 item test to check for sensory integration with balance. each of the 6 items is calculated for length of time and amount of sway. the less the sway, the lower the score and the better the balance. 2-6 months
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