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Sympathetic-Somatomotor Coupling in Human Spinal Cord Injury

Primary Purpose

Spinal Cord Injury

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Treadmill Training
Sponsored by
Shirley Ryan AbilityLab
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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

Arm Type

No Intervention

Experimental

Arm Label

One day testing

Effects of long term training

Arm Description

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

Outcomes

Primary Outcome Measures

Arterial blood flow
Subject will be tested with doppler ultrasonography immediately pre and post sympathetic stressor. Testing sessions will take anywhere between 3-6 hours.

Secondary Outcome Measures

Graded Treadmill Exercise Test
Graded treadmill exercise test will be tested at multiple intervals pre and post training paradigms.
Heart rate
Heart rate will be tested continuously during sympathetic stressors and at multiple intervals pre and post training paradigms with a Finapres.
Knee torque
Knee torque will be tested with the Biodex both pre and post sympathetic stressors.
Tendon tap reflexes
Tendon tap reflexes will be tested during one day testing pre and post sympathetic stressors.

Full Information

First Posted
April 14, 2014
Last Updated
April 30, 2021
Sponsor
Shirley Ryan AbilityLab
Collaborators
Marquette University
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1. Study Identification

Unique Protocol Identification Number
NCT02115685
Brief Title
Sympathetic-Somatomotor Coupling in Human Spinal Cord Injury
Official Title
Sympathetic-Somatomotor Coupling in Human Spinal Cord Injury
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Completed
Study Start Date
April 2014 (undefined)
Primary Completion Date
April 2020 (Actual)
Study Completion Date
April 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shirley Ryan AbilityLab
Collaborators
Marquette University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Significance: The long term objective of this study is to improve physical therapy and fitness programs in people with spinal cord injury. The results of the study will demonstrate the importance of matching blood flow to a muscle with exercise of that same muscle. 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.
Detailed Description
The regulation of cardiovascular systems during muscle activity is poorly understood in people with incomplete spinal cord injury (SCI). In the past, disruptions in somatomotor and sympathetic control have been investigated separately in SCI. We propose to investigate the coupling of sympathetic and somatomotor control because it is relevant to exercise training paradigms that are designed to improve somatomotor function or enhance physical fitness. Our approach will be to measure tendon tap reflexes, voluntary muscle activation, and blood flow of the knee (below injury) and elbow (above injury) before and after sympathetic stimuli consisting of cold pressor tests, mental math and an acute bout of exercise. These data will provide information about sympathetic control of blood flow during muscle activity. Plasticity of the sympatheticsomatomotor coupling will also be investigated by making measurements before and after a treadmill training exercise program. These experiments will enable us to address three aims. Aim 1 will be to characterize coupling of sympathetic and somatomotor systems below the level of spinal injury. This aim will examine spinal sympathetic and motor reflexes and their interactions. It will also examine how descending somatomotor coupling is disrupted by the spinal injury. In Aim 2, we will identify changes in the interactions of sympathetic and somatomotor systems above a spinal injury. Because of the injury and the changes that occur below the injury, the sympathetic-somatomotor coupling is also likely to be disrupted in the arm. Aim 3 will then demonstrate plasticity of sympathetic-somatomotor coupling after exercise training. Three different eight week exercise training programs will be tested including 1) treadmill training with exertion level matched to 70-80% of HRR 2)treadmill training with 30-40% HRR. The exercise training will be tested in a randomized crossover study design with one month between exercise training paradigms. We anticipate that there will be plasticity of sympathetic-somatomotor coupling and that the exercise training effects will normalize control of these systems. However, because of the injury, we anticipate that adaptations will differ from non-injured controls. 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spinal Cord Injury
Keywords
spinal cord injury, sympathetic nervous system, locomotor training, exercise

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
One day testing
Arm Type
No Intervention
Arm Description
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.
Arm Title
Effects of long term training
Arm Type
Experimental
Arm Description
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
Intervention Type
Other
Intervention Name(s)
Treadmill Training
Intervention Description
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.
Primary Outcome Measure Information:
Title
Arterial blood flow
Description
Subject will be tested with doppler ultrasonography immediately pre and post sympathetic stressor. Testing sessions will take anywhere between 3-6 hours.
Time Frame
6 hours
Secondary Outcome Measure Information:
Title
Graded Treadmill Exercise Test
Description
Graded treadmill exercise test will be tested at multiple intervals pre and post training paradigms.
Time Frame
15 months
Title
Heart rate
Description
Heart rate will be tested continuously during sympathetic stressors and at multiple intervals pre and post training paradigms with a Finapres.
Time Frame
15 months
Title
Knee torque
Description
Knee torque will be tested with the Biodex both pre and post sympathetic stressors.
Time Frame
8 hours
Title
Tendon tap reflexes
Description
Tendon tap reflexes will be tested during one day testing pre and post sympathetic stressors.
Time Frame
8 hours

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
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)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Brian D Schmidt, MD
Organizational Affiliation
Marquette University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
George Hornby, PT, PhD
Organizational Affiliation
University of Illinois at Chicago
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rehabilitation Institute of Chicago
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
32476619
Citation
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.
Results Reference
derived

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Sympathetic-Somatomotor Coupling in Human Spinal Cord Injury

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