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Clinical Trials/NCT01349478
NCT01349478
Completed
Phase 1

Electrical Stimulation Induced Lower Limb Exercise Capacity, Cardiorespiratory Response, Cardiovascular Risk Factors and Muscle Activity Patterns in Response to Robotic Assisted Treadmill Gait Training in Individuals With Complete Motor Spinal Cord Injury

Dr. Gabriel Zeilig1 site in 1 country11 target enrollmentMay 2011

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Motor Complete Spinal Cord Injury
Sponsor
Dr. Gabriel Zeilig
Enrollment
11
Locations
1
Primary Endpoint
Electrical stimulation induced lower limb exercise capacity in individuals with SCI
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to determine whether a three times per week, 2 month robotic assisted treadmill gait training program, will beneficially affect the fitness, physical and psychological well-being, and the vascular and metabolic cardiovascular risk factors in individuals with complete motor Spinal Cord Injury (SCI).

Detailed Description

Cardiovascular morbidity and mortality are a source of increasing concern among people with SCI and their health providers. The importance of physical activity in reducing the risk of heart disease in this population is indisputable, but exercise opportunities for persons with SCI are limited by physiologic and functional factors. Decreased functional muscle mass, impaired autonomic control of myocardial function, and decreased venous return limits training responses.

Registry
clinicaltrials.gov
Start Date
May 2011
End Date
May 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Dr. Gabriel Zeilig
Responsible Party
Sponsor Investigator
Principal Investigator

Dr. Gabriel Zeilig

Dr. Gabriel Zeilig

Sheba Medical Center

Eligibility Criteria

Inclusion Criteria

  • Male and non-pregnant non-lactating female
  • At least 6 months after injury
  • Complete (AIS A-B) cervical (C4-8) or thoracic (T1-T6) spinal cord injury according to American Spinal Injury Association (AIS) guidelines.
  • Under 100 kg and between 155 - 200 cm of height

Exclusion Criteria

  • History of severe neurological injuries other than SCI (MS, CP, ALS, TBI etc).
  • Severe concurrent medical diseases: infections, heart or lung, pressure sores, etc
  • Unstable spine or unhealed limbs or pelvic fractures
  • Psychiatric or cognitive situations that may interfere with the trial
  • Spasticity above 3 degree according to Ashworth scale
  • Reduced range of motion of knee/hip \> 15°

Outcomes

Primary Outcomes

Electrical stimulation induced lower limb exercise capacity in individuals with SCI

Time Frame: 4 and 8 weeks of training

The lower limb exercise capacity in response to electrical stimulation will be measured by the use of the ERGYS II system

Secondary Outcomes

  • Reduction of risk factors for CVD(4 and 8 weeks)

Study Sites (1)

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