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Clinical Trials/NCT02793635
NCT02793635
Completed
Not Applicable

Impact of Gait Training With an Exoskeleton on Walking Function After Spinal Cord Injury (SCI)

Parker Hannifin Corporation3 sites in 1 country9 target enrollmentJune 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Spinal Cord Injury
Sponsor
Parker Hannifin Corporation
Enrollment
9
Locations
3
Primary Endpoint
Functional ambulation category (FAC) to measure gait quality
Status
Completed
Last Updated
7 years ago

Overview

Brief Summary

The purpose of this study is to assess the use of Indego as a gait training tool for subjects with complete or incomplete paraplegia as a result of spinal cord injury (SCI) who have preserved lower extremity function. It is hypothesized that subjects with complete or incomplete paraplegia who have preserved their lower extremity function will experience functional improvements after gait training with the Indego exoskeleton.

Subjects will complete a total of fifteen (15) sessions which include a combination of the following; Physical Therapy Evaluation, Indego Training, Mid-Way Assessment, and Post-Assessment.

The aim of this study is to measure the impact of gait training with the Indego device on body structure, function, and participation. Additionally it will assess the perceptions of physical therapists and subjects with SCI on the effectiveness of gait training with the Indego exoskeleton in subjects with preserved limited function.

Registry
clinicaltrials.gov
Start Date
June 2016
End Date
March 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 18 years or older
  • Height 5'1" to 6'3" (Acceptable height may vary by a few inches depending on femur length)
  • Weight 250 lbs or less
  • Present with paraplegia resulting from a complete or incomplete (AIS A, B, C, or D) Spinal Cord Injury (\>1 year post-injury), with preserved LE function
  • Uses wheelchair as primary means of mobility in the community
  • Able to ambulate 14 meters with assist of 2 people and no orthostasis. Subjects may use any combination of stability aids and/or bracing.
  • Medical clearance for weight bearing and locomotor training
  • Bone density exams will be at the discretion of each sites' Principle Investigator
  • Passive range of motion (PROM) at shoulders, trunk, hips, knees and ankles within functional limits for safe gait and use of appropriate assistive device/stability aid
  • Skin intact where interfaces with the Indego device

Exclusion Criteria

  • Inability to meet ALL inclusion criteria
  • Currently participating in physical therapy for gait training
  • Joint contractures of the shoulders, trunk, hips knees or ankles deemed unsafe for locomotor training by PT and or MD
  • Edema that would put skin at risk for breakdown
  • Modified Ashworth Spasticity of 4
  • Inability to achieve adequate fit of the Indego device
  • Pregnancy
  • Colostomy bag

Outcomes

Primary Outcomes

Functional ambulation category (FAC) to measure gait quality

Time Frame: 1 Day

Categorizes patients according to basic motor skills necessary for functional ambulation

10 Meter Walking Test to measure fast gait speed

Time Frame: 1 Day

Assesses walking speed in meters per second over a short duration

6 Minute Walking test to measure endurance

Time Frame: 6 Minutes

Measures the distance an individual is able to walk over a total of six minutes on a hard, flat surface

Study Sites (3)

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