Actively Recruiting

Phase Not Applicable
Age: 18Years - 70Years
All Genders
NCT07128901

Lower-Limb Exoskeleton Technology for Non-Ambulatory Individuals With Spinal Cord Injury

Led by Georgia Institute of Technology · Updated on 2026-02-12

6

Participants Needed

1

Research Sites

50 weeks

Total Duration

On this page

Sponsors

G

Georgia Institute of Technology

Lead Sponsor

S

Shepherd Center, Atlanta GA

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this study is to compare two types of wearable lower-extremity exoskeletons -a self-balancing device lower-extremity exoskeleton and a user-balancing device lower-extremity exoskeleton-to better understand their effects on the physiological responses to walking and the user experience in people with spinal cord injury.

CONDITIONS

Official Title

Lower-Limb Exoskeleton Technology for Non-Ambulatory Individuals With Spinal Cord Injury

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Subacute to chronic spinal cord injury at least 3 months post injury
  • Motor-complete spinal cord injury classified as ASIA Impairment Scale A or B
  • Injury level between T3 and T11
  • Age between 18 and 70 years
  • Height between 5 feet 1 inch and 6 feet 1 inch
  • Weight less than 200 pounds (90 kg)
  • Seated hip width less than 42 cm
  • Able to stand for more than 15 minutes
  • Sufficient upper limb strength to use a platform rolling walker, rolling walker, or forearm crutches
  • Medically cleared and enrolled in the Shepherd Center Beyond Therapy program
  • Medically cleared for weight-bearing activities
  • Able to follow directions to safely participate in assessments
Not Eligible

You will not qualify if you...

  • Existing skin lesions or wounds
  • Hip or knee contracture greater than 10 degrees or ankle contracture greater than 5 degrees
  • Severe or uncontrolled spasticity
  • Non-healing fractures
  • Uncontrolled autonomic dysreflexia
  • Heart or peripheral vascular condition
  • Pregnancy
  • Active heterotopic ossification
  • Active deep vein thrombosis
  • Cognitive deficits that make it difficult to follow verbal instructions or make participation unsafe
  • Any safety concerns identified by the principal investigator

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The Shepherd Center

Atlanta, Georgia, United States, 30332

Actively Recruiting

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Research Team

M

Maegan Tucker, PhD

CONTACT

N

Nick Evans, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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