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

Evaluation of the Short Effects of a Rehabilitation Session on Gait Parameters in Patients With a Lesion of the Central Nervous System

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01807247
Enrollment
60
Registered
2013-03-08
Start date
2013-02-28
Completion date
2014-10-31
Last updated
2015-02-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fall Due to Failure of Support, Fatigue, Spastic Gait

Keywords

Strengthening muscle, Central nervous system diseases, Gait

Brief summary

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.

Interventions

PROCEDUREIntensive lower limbs muscles strengthening

Sponsors

Centre d'Investigation Clinique et Technologique 805
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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)

Design outcomes

Primary

MeasureTime frameDescription
Evaluation of functional capacity after rehabilitation session using functional tests such as 6 minutes walking test and timed up and go30 minclinical exam, timed up and go, stair test, 6 minutes walking test

Secondary

MeasureTime frameDescription
Evaluation of gait pattern and muscle activation patterns during video and EMG analyzes.1 hourEMG analysis of rectus femoris, hamstrings, tibialis anterior and soleus

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026