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

Sponsor
Centre d'Investigation Clinique et Technologique 805 (Other)
Overall Status
Completed
CT.gov ID
NCT01807247
Collaborator
(none)
60
1
19.9
3

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,

  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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Intensive lower limbs muscles strengthening

Study Design

Study Type:
Observational
Actual Enrollment :
60 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Evaluation of the Short Effects of a Rehabilitation Session on Gait Parameters in Patients With a Lesion of the Central Nervous System
Study Start Date :
Feb 1, 2013
Actual Primary Completion Date :
Oct 1, 2014
Actual Study Completion Date :
Oct 1, 2014

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

  1. 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

  1. 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

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts 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)

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.
Responsible Party:
Nicolas ROCHE, MDPHD, Centre d'Investigation Clinique et Technologique 805
ClinicalTrials.gov Identifier:
NCT01807247
Other Study ID Numbers:
  • 2011-A01487-34
First Posted:
Mar 8, 2013
Last Update Posted:
Feb 4, 2015
Last Verified:
Mar 1, 2013
Keywords provided by Nicolas ROCHE, MDPHD, Centre d'Investigation Clinique et Technologique 805
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 4, 2015