Multiple Sclerosis Clinical Trial
Randomised double blind study of two parallel groups,one of the groups trained with the full
APOS kit (a shoe with an additional bio mechanical device)
The control group trained with the Apos shoe without the bio mechanical device. both groups
will be checked at the beginning of the study, one month later and at the end of the study
after two months. The tests include neurological test, functional test(FSST,up and go test
and berg balance test) gate analysis and quality fo life (rays) test.
Status | Recruiting |
Enrollment | 30 |
Est. completion date | October 2006 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - diagnosis of Multiple sclerosis Cerebellar impairment EDSS under 4.5 age 18-65 years signed informed consent form Exclusion Criteria: - pregnancy - coronary event in last 6 month - 30 days or less after acute attack - steroidal treatment in the last 60 days - alcohol abuse |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Israel | Sheba Medical Center | Ramat Gan |
Lead Sponsor | Collaborator |
---|---|
Sheba Medical Center |
Israel,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | functional tests | |||
Secondary | gait analysis |
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