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Behavioural Intervention
Control Group training for Spinal Cord Injury
Phase 4
Waitlist Available
Led By Milos Popovic, PhD
Research Sponsored by Ontario Neurotrauma Foundation
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
incomplete spinal cord lesion of sudden onset between C6 and T12 that is motor incomplete (grade C or D on the ASIA neurological impairment scale). The injury must have occurred at least two years prior to recruitment
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 4, 6 and 12 months
Awards & highlights
Study Summary
The purpose of this study is to evaluate whether an aerobic and resistance training program or a functional electrical stimulation-assisted Walking program is more effective for reducing health complications related to spinal cord injury, for example, the occurrence of bladder infections, pressure sores and/or frequency of spasms. It is hypothesized that the functional electrical stimulation-assisted walking will have a greater impact on secondary complications than the aerobic and resistance training program.
Eligible Conditions
- Spinal Cord Injury
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, 4, 6 and 12 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 4, 6 and 12 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Bone density at different hip, spine, proximal and distal femur and proximal Tibia using dual-energy xray absorptiometry
Bone density, bone geometry and muscle area via computed tomography
Factor analysis of electromyography and kinematics of gait.
+2 moreSecondary outcome measures
Craig Handicap assessment and reporting technique,
Incidence of pressure sores
Incidence of urinary tract infections
+7 moreTrial Design
2Treatment groups
Experimental Treatment
Group I: FES trainingExperimental Treatment1 Intervention
Arm 1 receives functional electrical stimulation while walking on body weight suspension training.
Group II: Control Group trainingExperimental Treatment1 Intervention
Aerobic and resistance training program
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Who is running the clinical trial?
Ontario Neurotrauma FoundationLead Sponsor
22 Previous Clinical Trials
1,071 Total Patients Enrolled
Milos Popovic, PhDPrincipal InvestigatorUniversity of Toronto
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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