Spinal Cord Injuries Clinical Trial
Official title:
Non-Invasive Stimulation for Improving Motor Function in Spinal Cord Injury
NCT number | NCT03592173 |
Other study ID # | BRC391 |
Secondary ID | |
Status | Recruiting |
Phase | Phase 2 |
First received | |
Last updated | |
Start date | July 2013 |
Est. completion date | December 2019 |
The purpose of this study is to determine if spinal excitability is increased with a Spinal Associative Stimulation (SAS) protocol, and to determine the functional consequences of this technique on motor recovery.
Status | Recruiting |
Enrollment | 30 |
Est. completion date | December 2019 |
Est. primary completion date | September 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 80 Years |
Eligibility |
Inclusion Criteria: - Spinal cord injury subjects with chronic lesions (> 6 months after the injury) - Motor incomplete lesion, measured by the American Spinal cord Injury Association (ASIA) Impairment Scale (AIS) - Traumatic cause of lesion; d) Some degree of motor function in the ankle flexor and extensors (Low extremity Motor Score - LEMS=3). Exclusion Criteria: - Motor and sensory complete lesion (AIS A); LEMS < 3; - Non-traumatic cause of lesion - Medically unstable condition - Other concurrent neurological illness - Presence of a potential TMS risk factor (detailed below) Potential TMS risk factor: - Damaged skin at the site of stimulation - Presence of an electrically, magnetically or mechanically activated implant - An intracerebral vascular clip, or any other electrically sensitive support system - Metal in any part of the body, including metal injury to the eye - A history of medication-resistant epilepsy in the family - Past history of seizures or unexplained spells of loss of consciousness. |
Country | Name | City | State |
---|---|---|---|
United States | Burke Medical Research Institute | White Plains | New York |
Lead Sponsor | Collaborator |
---|---|
Kathleen Friel | Burke Medical Research Institute |
United States,
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* Note: There are 14 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in H-Reflex Threshold | Assessment of muscle reaction after stimulation of sensory fibers | Baseline compared with immediately after intervention | |
Secondary | Lower Extremity Motor Score (LEMS) | Assessment of lower extremity strength in key muscles; maximal score of 50 with 20 or less indicating participant likely has limited ambulation. | Baseline, immediately after intervention | |
Secondary | Walking Index for Spinal Cord Injury (WISCI II) | This is a functional capacity scale that rank orders ambulation in people with spinal cord injury, by evaluating the amount of physical assistance, braces or devices required to walk 10 meters. Rank scores range from 0-20. A higher score is indicative of more independent ambulation. | Baseline, immediately after intervention | |
Secondary | 10 Meter Walk Test | Measure of gait speed | Baseline, immediately after intervention | |
Secondary | Spinal Cord Independence Measure, Version 3 (SCIM III) | A disability rating scale developed to specifically address the ability of SCI patients to perform basic activities of daily living independently (including self-care, mobility, respiration and sphincter management) | Baseline, immediately after intervention | |
Secondary | Muscle Force | Amount of force recorded during maximal voluntary isometric contraction of a grip movement, recorded with a grip strength measurement device. | Baseline, immediately after intervention | |
Secondary | Anklebot | Lower extremity robotic device that provides kinematic evaluation data | Baseline, immediately after intervention |
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