Sympathetic-Somatomotor Coupling in Human Spinal Cord Injury
NCT ID: NCT02115685
Last Updated: 2021-05-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
40 participants
INTERVENTIONAL
2014-04-30
2020-04-30
Brief Summary
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Scientific Objective: The objective of the study is to measure how the body regulates bloodflow to a muscle during exercise. We intend to study these effects by triggering blood flow changes during movement, and measuring bloodflow changes during exercise in people with spinal cord injury. We will also look at the long term effects of different exercise programs on bloodflow during exercise.
Study Populations: This study will involve people with partial spinal cord injury and age and sex matched controls without injury.
Specific Aims: 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 2 will then look at changes in bloodflow during exercise after training. Three different eight week exercise training programs will be tested including 1) upper body ergometry, 2) treadmill training with exertion level matched to the upper body ergometry and 3) treadmill training with heart rate matched to an initial test of upper body ergometry.
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Detailed Description
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This study has implications for exercise training in human SCI. The coupling of sympathetic and somatomotor systems is expected to depend on whether exercise targets the upper or lower body. The recovery of function requires both the improvement in the control of movement as well as in the regulation of blood flow to active muscle groups. In addition, this study is important for understanding the potential impact of treadmill exercise training on cardiovascular fitness, a topic of increasing interest in people with limitations to physical activity.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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One day testing
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.
No interventions assigned to this group
Effects of long term training
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
Treadmill Training
Subjects will be randomized to a high intensity and low intensity group. The high intensity group will train at 70-80% of their HRR and the low intensity group will train at 30-40% of their HRR.
Interventions
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Treadmill Training
Subjects will be randomized to a high intensity and low intensity group. The high intensity group will train at 70-80% of their HRR and the low intensity group will train at 30-40% of their HRR.
Eligibility Criteria
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Inclusion Criteria
* 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
* 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)
18 Years
75 Years
ALL
Yes
Sponsors
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Marquette University
OTHER
Shirley Ryan AbilityLab
OTHER
Responsible Party
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Thomas G Hornby
PT, PhD
Principal Investigators
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Brian D Schmidt, MD
Role: PRINCIPAL_INVESTIGATOR
Marquette University
George Hornby, PT, PhD
Role: PRINCIPAL_INVESTIGATOR
University of Illinois at Chicago
Locations
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Rehabilitation Institute of Chicago
Chicago, Illinois, United States
Countries
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References
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Lotter JK, Henderson CE, Plawecki A, Holthus ME, Lucas EH, Ardestani MM, Schmit BD, Hornby TG. Task-Specific Versus Impairment-Based Training on Locomotor Performance in Individuals With Chronic Spinal Cord Injury: A Randomized Crossover Study. Neurorehabil Neural Repair. 2020 Jul;34(7):627-639. doi: 10.1177/1545968320927384. Epub 2020 Jun 1.
Other Identifiers
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