Evaluation of a Training in the Walking With Exosquelette (LOKOMAT)

March 1, 2016 updated by: Nicolas ROCHE, Centre d'Investigation Clinique et Technologique 805
Stroke patients in the investigators rehabilitation unit follow gait trainings with robotic-assistive devices such as Lokomat. Patients able to walk alone are also assessed with 3D gait analysis. The objective of this study is to assess the effects of gait training in Lokomat on biomecanic gait parameters in stroke patients.

Study Overview

Status

Completed

Conditions

Study Type

Observational

Enrollment (Actual)

13

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • France
      • Garches, France, 92380
        • Hôpital Raymond Poincaré

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

stroke patients follow in our rehabilitation hospital, able to walk alone

Description

Inclusion Criteria:

  • single stroke
  • able to walk alone
  • > 18years

Exclusion Criteria:

  • Cognitive impairments disturbing understanding
  • Uncontrolled medical disorder associated

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
peak knee flexion (degrees)
Time Frame: participants will be followed for the duration of hospital stay, an expected average of 1 week
participants will be followed for the duration of hospital stay, an expected average of 1 week

Secondary Outcome Measures

Outcome Measure
Time Frame
hip and ankle kinematics (degrees)
Time Frame: participants will be followed for the duration of hospital stay, an expected average of 1 week
participants will be followed for the duration of hospital stay, an expected average of 1 week
kinetics (newton/meter)
Time Frame: participants will be followed for the duration of hospital stay, an expected average of 1 week
participants will be followed for the duration of hospital stay, an expected average of 1 week
spatio temporal parameter (m/s)
Time Frame: participants will be followed for the duration of hospital stay, an expected average of 1 week
participants will be followed for the duration of hospital stay, an expected average of 1 week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Centre d'Investigation Clinique et Technologique 805

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

October 1, 2013

Primary Completion (ACTUAL)

December 1, 2015

Study Completion (ACTUAL)

December 1, 2015

Study Registration Dates

First Submitted

January 28, 2014

First Submitted That Met QC Criteria

March 11, 2014

First Posted (ESTIMATE)

March 13, 2014

Study Record Updates

Last Update Posted (ESTIMATE)

March 2, 2016

Last Update Submitted That Met QC Criteria

March 1, 2016

Last Verified

October 1, 2015

More Information

Terms related to this study

Other Study ID Numbers

  • 12077 (Korea FDA)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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