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Exoskeleton for Post-Stroke Recovery of Ambulation

NCT02995265 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2020-08-31

No results posted yet for this study

Summary

To determine the effect of using a robotic exoskeleton to allow walking practice after stroke, compared to usual physiotherapy care, on recovery of walking ability and secondary outcomes.

Conditions

  • Conditions

Interventions

DEVICE

Exoskeleton Program

Subjects will wear the exoskeleton device at each physiotherapy session to work on improving mobility and walking ability.

OTHER

Usual Care Program

Subjects will receive hands-on physiotherapy to improve their mobility and walking ability. Physiotherapy session will be tailored to subject individually by their therapist.

Sponsors & Collaborators

  • Heart and Stroke Foundation of Canada

    collaborator OTHER

  • University of British Columbia

    lead OTHER

Principal Investigators

  • Janice J Eng, PhD · Department of Physical Therapy, University of British Columbia

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-05-01
Primary Completion
2020-02-08
Completion
2020-06-30
FDA Device
Yes

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02995265 on ClinicalTrials.gov