Short Effects of a Rehabilitation Session on Gait in Patients With CNS

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

60 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-02-28

Study Completion Date

2014-10-31

Brief Summary

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The aim of the study is to evaluate the short effects of a two rehabilitation session commonly performed in physical therapy,

1. muscle strengthening of the lower limbs and
2. effort reconditioning with cyclo ergometer, on gait characteristics (kinematics, kinetics and electromyographic) in patients with central nervous system lesion.

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Detailed Description

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Conditions

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Spastic Gait Fall Due to Failure of Support Fatigue

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Hemiparetic

Intensive lower limbs muscles strengthening

Intervention Type PROCEDURE

Spinal cord injury

Intensive lower limbs muscles strengthening

Intervention Type PROCEDURE

Multiple sclerosis

Intensive lower limbs muscles strengthening

Intervention Type PROCEDURE

Interventions

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Intensive lower limbs muscles strengthening

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Male or female adults aged ≥ 18 years receiving a motor rehabilitation in the service
* Hemiplegia after stroke or paraplegia incomplete ASIA C or D or multiple sclerosis (EPSS \<5).
* Walking with or without technical assistance
* Patients who received and signed information and informed consent
* Patient who received physiotherapy session for rehabilitation of the lower limbs
* Patients able to perform the entire study

Exclusion Criteria

* Patient with safety measure
* Pregnant women, breastfeeding
* Patient who has received botulinum toxin injection of in the lower limbs between 3 weeks and 2 months prior to inclusion in the study
* Bilateral Brain damage, cerebellar syndrome, apraxia, severe aphasia
* Orthopedic complications preventing walking
* Patients who participated in a clinical study within 3 months prior to inclusion • No affiliation to a social security scheme (beneficiary or assignee)

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No