Sympathetic-Somatomotor Coupling in Human Spinal Cord Injury
Spinal Cord Injury
About this trial
This is an interventional treatment trial for Spinal Cord Injury focused on measuring spinal cord injury, sympathetic nervous system, locomotor training, exercise
Eligibility Criteria
Inclusion Criteria:
- incomplete SCI
- subjects will be over age 18
- to fit in the apparatus and to assure a mature gait pattern
- at least 6 months post injury, and medically stable with an incomplete lesion between levels T1-T10
- lower extremity motor score of 10 or greater
- presence of intact stretch reflexes, detected clinically
- no previous history or evidence of peripheral nerve damage in the lower extremities
- Subjects must be able to step on a treadmill with no more than 40% body weight support.
Healthy controls will be age and sex matched to the subjects with spinal cord injury.
Exclusion Criteria:
- unhealed decubiti,
- bladder or other infection
- severe contracture or osteoporosis
- heterotopic ossification
- cardiac arrhythmia
- inability to give informed consent
- an episode of autonomic dysreflexia in the past year
- use of spasticity or cardiovascular medications (e.g. baclofen)
Sites / Locations
- Rehabilitation Institute of Chicago
Arms of the Study
Arm 1
Arm 2
No Intervention
Experimental
One day testing
Effects of long term training
Aim 1 will be to measure bloodflow during exercise of the legs (below the injury). This aim will examine the control of bloodflow and muscle contractions and how it changes after spinal cord injury.
Aim 3 will then look at changes in bloodflow during exercise after training. Three different eight week exercise training programs will be tested including 1) treadmill training at high intensity as defined by 70-80% of HRR or 15-17 RPE 2) treadmill training at low intensity as defined by 30-40% of HRR or <13 RPE