Short Effects of a Rehabilitation Session on Gait in Patients With CNS
Study Details
Study Description
Brief Summary
The aim of the study is to evaluate the short effects of a two rehabilitation session commonly performed in physical therapy,
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muscle strengthening of the lower limbs and
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effort reconditioning with cyclo ergometer, on gait characteristics (kinematics, kinetics and electromyographic) in patients with central nervous system lesion.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Study Design
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
Hemiparetic Intensive lower limbs muscles strengthening |
Procedure: Intensive lower limbs muscles strengthening
|
Spinal cord injury Intensive lower limbs muscles strengthening |
Procedure: Intensive lower limbs muscles strengthening
|
Multiple sclerosis Intensive lower limbs muscles strengthening |
Procedure: Intensive lower limbs muscles strengthening
|
Outcome Measures
Primary Outcome Measures
- Evaluation of functional capacity after rehabilitation session using functional tests such as 6 minutes walking test and timed up and go [30 min]
clinical exam, timed up and go, stair test, 6 minutes walking test
Secondary Outcome Measures
- Evaluation of gait pattern and muscle activation patterns during video and EMG analyzes. [1 hour]
EMG analysis of rectus femoris, hamstrings, tibialis anterior and soleus
Eligibility Criteria
Criteria
Inclusion Criteria:
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Male or female adults aged ≥ 18 years receiving a motor rehabilitation in the service
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Hemiplegia after stroke or paraplegia incomplete ASIA C or D or multiple sclerosis (EPSS <5).
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Walking with or without technical assistance
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Patients who received and signed information and informed consent
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Patient who received physiotherapy session for rehabilitation of the lower limbs
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Patients able to perform the entire study
Exclusion Criteria:
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Patient with safety measure
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Pregnant women, breastfeeding
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Patient who has received botulinum toxin injection of in the lower limbs between 3 weeks and 2 months prior to inclusion in the study
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Bilateral Brain damage, cerebellar syndrome, apraxia, severe aphasia
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Orthopedic complications preventing walking
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Patients who participated in a clinical study within 3 months prior to inclusion • No affiliation to a social security scheme (beneficiary or assignee)
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Hopital Raymond Poincare | Garches | France | 92380 |
Sponsors and Collaborators
- Centre d'Investigation Clinique et Technologique 805
Investigators
- Principal Investigator: Nicolas ROCHE, MDPHD, Hôpital RAYMOND POINCARE
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 2011-A01487-34