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Clinical Trials/NCT00843128
NCT00843128
Completed
Phase 2

Phase II Study of the Effectiveness of Locomotor Therapy Using Robot-Driven Gait Orthosis System in Acute Stroke Patients: A Randomized Controlled Trial.

Hadassah Medical Organization1 site in 1 country40 target enrollmentMarch 2009

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Multiple Sclerosis
Sponsor
Hadassah Medical Organization
Enrollment
40
Locations
1
Primary Endpoint
Functional Ambulatory Capacity (FAC) scale and the 6-minutes walking distance
Status
Completed
Last Updated
15 years ago

Overview

Brief Summary

Objective: To evaluate the efficacy of robot-assisted gait training (RAGT) in MS patients with severe walking disabilities (Expanded Disability Status Scale [EDSS] 5.5-7) as compared to regular physiotherapy.

Methods: Prospective, randomized, controlled clinical trial comparing RAGT with conventional walking training (CWT) in a group of stable MS patients (n=40) during an outpatient rehabilitation program. Inclusion criteria are chronic or secondary progressive MS patients with EDSS between 5.5-7, stable treatment 3 months before study entry, without generalized diseases. All patients will sign an informed consent. Following randomization, 20 patients will be treated with RAGT, 12 sessions over three weeks. The control group will be treated by CWT, 12 sessions in three weeks. The primary outcome measures will be the Functional Ambulatory Capacity (FAC) scale and the 6-minutes walking distance. The secondary outcome measures will be the Time up & Go (TUG) test, 10 Meter Walking test, Berg balance test, EDSS score, FIM score and RAND questioner for quality of life. All tests will be performed by an external blinded assessor at baseline, after three weeks, and at follow-up after 3 months and six months.

Importance: We anticipated that Robot-assisted gait training will be found as feasible and may be an effective therapeutic option in MS patients with severe walking disabilities.

Registry
clinicaltrials.gov
Start Date
March 2009
End Date
August 2010
Last Updated
15 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • chronic or secondary progressive MS patients with EDSS between 5.5-7,
  • stable treatment 3 months before study entry.

Exclusion Criteria

  • Other generalized diseases.

Outcomes

Primary Outcomes

Functional Ambulatory Capacity (FAC) scale and the 6-minutes walking distance

Time Frame: At baseline, after three weeks, and at follow-up after 3 months and six months.

Secondary Outcomes

  • Time up & Go (TUG) test, 10 Meter Walking test, Berg balance test, EDSS score, FIM score and SF36 questioner for quality of life.(At baseline, after three weeks, and at follow-up after 3 months and six months.)

Study Sites (1)

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