Robot-assisted Gait Training in Patients With Multiple Sclerosis: Efficacy and Comparison With Traditional Methods
Multiple Sclerosis

About this trial
This is an interventional treatment trial for Multiple Sclerosis focused on measuring Gait orthosis, Lokomat, Robotic Rehabilitation
Eligibility Criteria
Inclusion Criteria:
- diagnosis of multiple sclerosis according to the McDonald's Criteria in stable phase of disease for at least 3 months.
- ability to walk 25 foot without assistance
- EDSS score between 3.5 and 7
Exclusion Criteria:
- exacerbations of the disease in the last 3 months
- deficits of somatic sensation involving the legs
- other neurological, orthopedic or cardiovascular co-morbility
- severe posture abnormalities
- severe-moderate cognitive impairment (Mini Mental State ≤ 21)
- body weight greater than 135 kg;
- height more than 200 cm;
- limb-length discrepancy greater than 2 cm;
- presence of skin lesions on the trunk, pelvis and lower limbs that could interfere with the placement of the electrodes and straps anchoring the Lokomat.
Sites / Locations
- HABILITARecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Experimental group
Control group
Participants received 25 sessions of robotically driven gait orthosis training on the Lokomat. Training occurred approximately 5 days/ week for 5 weeks, and each training session on the Lokomat lasted 30 minutes. All sessions were supervised by a trained research therapist. All participants started with 40% body weight-support and an initial treadmill speed of 1.5 km/h. Body weight-support was used primarily to facilitate an increase in walking speed; therefore, progression of training across subsequent sessions was standardized by preferentially increasing speed and then unloading body weight-support. Speed was increased to a range of 2.2 to 2.5 km/h before body weight-support was decreased. There was an active attempt to enhance the level of training at each session. After every Lokomat session, participants performed also 60 minutes of physiotherapy including general exercise program and a conventional gait training
Participants received 25 sessions of conventional physiotherapy. Training occurred approximately 5 days/week for 5 weeks, and each training session lasted 1 hour and half. Patients allocated to the Control Group performed the same conventional physiotherapy training of the other group: a general exercise program and a conventional gait training. The general exercise program consisted in cardiovascular warm-up exercises, muscle stretching exercises, active-assisted or active isometric and isotonic exercises for the main muscles of the trunk and limbs, relaxation exercises, coordination and static/dynamic balance exercises. The conventional gait therapy was based on the proprioceptive neuromuscular facilitation concept, training in walking on different surfaces with or without appropriate walking aids, exercises for the restoration of a correct gait pattern, implementation of residual compensatory strategies and progressive increase of walking resistance