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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02900508
Other study ID # 201410010A
Secondary ID
Status Completed
Phase N/A
First received September 6, 2016
Last updated September 8, 2016
Start date October 2014
Est. completion date September 2015

Study information

Verified date September 2016
Source National Yang Ming University
Contact n/a
Is FDA regulated No
Health authority Taiwan: Ministry of Health and Welfare
Study type Interventional

Clinical Trial Summary

The purpose of this study was to investigate the effects of virtual reality-base training for cerebellar ataxia.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date September 2015
Est. primary completion date July 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- diagnosis of SCA 1, 2, 3 and 6 by a neurologist

- ability to walk independently with or without any walking aids

- age = 20

- a score of = 24 on the mini-mental state examination

Exclusion Criteria:

- histories of other neurological, cardiovascular, or orthopedic diseases affecting motor performance and balance

- uncontrolled chronic diseases

Study Design

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


Related Conditions & MeSH terms


Intervention

Other:
Exergaming training

Physical therapy intervention


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
National Yang Ming University

Outcome

Type Measure Description Time frame Safety issue
Primary Scale for the Assessment and Rating of Ataxia Change from baseline at 4 weeks
Primary Alternate nose to finger test Change from baseline at 4 weeks
Primary Alternate heel on shin test Change from baseline at 4 weeks
Secondary Nine-hole peg test Change from baseline at 4 weeks
Secondary Walking speed Change from baseline at 4 weeks
Secondary Step width Change from baseline at 4 weeks
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