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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT03436927 |
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Date of registration:
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11/12/2017 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Comparison of Two Different Virtual Reality Methods in Patients With Multiple Sclerosis
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Scientific title:
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Comparison of the Effects of Two Different Virtual Reality Treatment Methods in Patients With Multiple Sclerosis: A Randomized Controlled Trial |
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Date of first enrolment:
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July 15, 2016 |
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Target sample size:
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51 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT03436927 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Double (Investigator, Outcomes Assessor).
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Phase:
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N/A
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- . Participants who were ambulatory and volunteer to participate to the study, in a
stable phase of the disease, without relapses or worsening in the last 3 months, with
an EDSS between 2.5-6 and aged between 25 to 60 years
Exclusion Criteria:
- physical activity more than 150 minutes per week, were pregnant, had blurred vision,
had psychiatric problems, or severe cognitive impairment.
Age minimum:
25 Years
Age maximum:
60 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Multiple Sclerosis
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Intervention(s)
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Other: Nintendo Wii Fit Balance exercises
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Other: Balance Trainer Balance Exercises
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Primary Outcome(s)
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Berg Balance Scale
[Time Frame: Change between baseline and after 8 weeks of intervention were assessed.]
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Secondary Outcome(s)
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Fatigue Severity Scale
[Time Frame: Change between baseline and after 8 weeks of intervention were assessed.]
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Six Minutes Walk Test
[Time Frame: Change between baseline and after 8 weeks of intervention were assessed.]
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Timed Up and Go Test
[Time Frame: Change between baseline and after 8 weeks of intervention were assessed.]
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Secondary ID(s)
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YZenginler
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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