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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 below

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 4, 6 and 12 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, 4, 6 and 12 months for reporting.

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 more
Secondary outcome measures
Craig Handicap assessment and reporting technique,
Incidence of pressure sores
Incidence of urinary tract infections
+7 more

Trial 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

Find a Location

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.
~2 spots leftby Apr 2025