Evaluation of a Training in the Walking With Exosquelette

Stroke Clinical Trial

— LOKOMAT  

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02085954
• Other study ID #: 12077
• Status: Completed
• Phase: N/A
• First received: January 28, 2014
• Last updated: March 1, 2016
• Start date: October 2013
• Est. completion date: December 2015

Study information

• Verified date: October 2015
• Source: Centre d'Investigation Clinique et Technologique 805
• Contact: n/a
• Is FDA regulated: No
• Health authority: France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
• Study type: Observational

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 13
• Est. completion date: December 2015
• Est. primary completion date: December 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• single stroke

• able to walk alone

• > 18years

Exclusion Criteria:

• Cognitive impairments disturbing understanding

• Uncontrolled medical disorder associated

Study Design

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

• Gait
• Robotic Rehabilitation
• Stroke

Locations

Country	Name	City	State
France	Hopital Raymond Poincare	Garches

Sponsors (1)

Lead Sponsor	Collaborator
Centre d'Investigation Clinique et Technologique 805

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	peak knee flexion (degrees)		participants will be followed for the duration of hospital stay, an expected average of 1 week	No
Secondary	hip and ankle kinematics (degrees)		participants will be followed for the duration of hospital stay, an expected average of 1 week	No
Secondary	kinetics (newton/meter)		participants will be followed for the duration of hospital stay, an expected average of 1 week	No
Secondary	spatio temporal parameter (m/s)		participants will be followed for the duration of hospital stay, an expected average of 1 week	No