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Clinical Trials/NCT02821845
NCT02821845
Completed
Not Applicable

Eccentric Motor Control Training to Improve Human Spinal Cord Injury: Observation of Hip and Knee Function

Ohio State University1 site in 1 country49 target enrollmentJune 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Spinal Cord Injury
Sponsor
Ohio State University
Enrollment
49
Locations
1
Primary Endpoint
Change from baseline in time to complete 6 minutes of level walking (i.e., the 6 minute walk test)
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

This project will characterize lower extremity eccentric muscle function among individuals who have undergone locomotor training after spinal cord injury and will evaluate the effect of downhill training at slow to moderate speeds - targeted to rehabilitation eccentric function of the hip and knee.

Detailed Description

Lower extremity eccentric motor control is is critically important for locomotor function but is impaired after spinal cord injury (SCI). Even after treadmill training, preliminary evidence indicates that eccentric deficits persist among individuals with SCI. This proposal aims to characterize eccentric motor control of the muscles about the hip and knee during locomotion and evaluate the efficacy of downhill gait training at slow speeds as an intervention to improve eccentric function of the hip joint and knee joint during walking.

Registry
clinicaltrials.gov
Start Date
June 2015
End Date
October 2019
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Michele Basso

Professor

Ohio State University

Eligibility Criteria

Inclusion Criteria

  • medically approved
  • discharged from outpatient rehabilitation for 6 months
  • incomplete SCI based on ASIA impairment score (AIS C or D) at neurologic level C1-T10
  • ability to take some steps overground and on the treadmill
  • 18-90 years old.
  • ability to speak English. Note: the quality of life measures have not been validated yet in non-English speaking populations.

Exclusion Criteria

  • evidence of lower motor neuron injury in the legs
  • use of botox in the past 3 months
  • pre-existing or confounding neurologic conditions (i.e. brain injury, stroke, HIV)
  • acute deep vein thrombosis
  • skin wounds in regions where harness or hands provide support
  • pregnancy. Note: Persons who are pregnant will not be enrolled as exercise tolerance is unknown in these women with SCI.
  • cognitive conditions that preclude providing informed consent
  • ventilator-dependence as study results will be confounded by mobility limitations imposed by equipment
  • persistent orthostatic hypotension (drop of BP \>30mmHg in treadmill and harness equipment)
  • hospitalization for myocardial infarction, cardiac surgery or congestive heart failure exacerbation within 3 months of enrollment in study

Outcomes

Primary Outcomes

Change from baseline in time to complete 6 minutes of level walking (i.e., the 6 minute walk test)

Time Frame: baseline, 12 weeks

Secondary Outcomes

  • Change from baseline in time to complete 10 meters of level walking (i.e., the 10 meter walk test)(baseline, 12 weeks)
  • Change from baseline in peak magnitude of frontal hip loading response as measured by the peak magnitude of frontal hip power absorption during the weight acceptance phase of walking(baseline, 12 weeks)

Study Sites (1)

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