Can Arm and Leg Cycling Exercise Improve Walking After Stroke

December 11, 2014 updated by: Dr. E. Paul Zehr, University of Victoria

Can Arm and Leg Cycling Exercise Improve Walking After Stroke?

It has been found that arm and leg cycling is similar to walking. Thus, the objective of this research is to determine if arm and leg cycling can be used to improve walking ability in a post-stroke population. This outcome would directly impact the health and quality of life for those who have suffered a stroke.

Study Overview

Detailed Description

It has been found that arm and leg cycling is similar to walking in terms of the muscle activation patterns, joint ranges of motion, and neural pathways activated. Another advantage of arm and leg cycling is that it involves coordination of all four limbs in a rhythmic movement. This may be particularly beneficial given previous findings that arm movement contributes to the activation of leg muscles during walking in humans. This is achieved with interconnected neural pathways that link the arms to the legs. These neural interlimb connections remain intact in stroke victims, such that maximizing the contribution of the arms to the legs may increase coordination for walking.

Thus, the objective of this research is to determine if arm and leg cycling can be used to increase the strength of inter-limb connections and if this helps to improve walking ability in a post-stroke population. 15-20 participants will be recruited to participate in a five week training intervention where measures will be taken before and after the intervention to assess efficacy. Arm and leg cycling could provide a novel method to improve inter-limb coupling and walking ability. These outcomes would directly impact the health and quality of life for those who have suffered a stroke.

Study Type

Interventional

Enrollment (Anticipated)

20

Phase

  • Not Applicable

Contacts and Locations

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

Study Contact

  • Name: E P Zehr, Doctorate
  • Phone Number: (250) 472-5487
  • Email: rnl@uvic.ca

Study Locations

    • British Columbia
      • Victoria, British Columbia, Canada
        • Recruiting
        • MacLaurin Building
        • Contact:
          • Taryn Klarner, Masters
          • Phone Number: (250) 472-5487
          • Email: rnl@uvic.ca
        • Sub-Investigator:
          • Taryn Klarner, Masters

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Cerebrovascular accident

Exclusion Criteria:

  • Inability to stand

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

  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Test Group
5 weeks of arm and leg cycling, 3 times per week for 30 minute of total exercise per session

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Walking Ability
Time Frame: Within five days
Treadmill test of walking coordination, speed, and symmetry. Interlimb coordination assessed with peripheral nerve stimulation during arm and leg cycling and walking. Strength of dorsi-flexion and plantar-flexion and grip strength also assessed.
Within five days

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Clinical Status assessed by a Physiotherapist
Time Frame: Within 5 days
Clinical assessment of skin sensitivity, spasticity, balance and coordination, and walking endurance.
Within 5 days

Collaborators and Investigators

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

Investigators

  • Principal Investigator: E P Zehr, Doctorate, University of Victoria

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

July 1, 2011

Primary Completion (Anticipated)

December 1, 2014

Study Completion (Anticipated)

December 1, 2015

Study Registration Dates

First Submitted

December 9, 2014

First Submitted That Met QC Criteria

December 11, 2014

First Posted (Estimate)

December 12, 2014

Study Record Updates

Last Update Posted (Estimate)

December 12, 2014

Last Update Submitted That Met QC Criteria

December 11, 2014

Last Verified

December 1, 2014

More Information

Terms related to this study

Other Study ID Numbers

  • D015017-2011-2014
  • 123456 (UMMashhad)

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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