Actively Recruiting

Phase Not Applicable
Age: 16Years - 85Years
All Genders
NCT05218447

Dosing of Overground Robotic Gait Training with Functional Outcomes and Neuroplasticity After Spinal Cord Injury

Led by Baylor Research Institute · Updated on 2025-02-06

144

Participants Needed

1

Research Sites

173 weeks

Total Duration

On this page

Sponsors

B

Baylor Research Institute

Lead Sponsor

U

United States Department of Defense

Collaborating Sponsor

AI-Summary

What this Trial Is About

The DOOR SCI project examines dosing effects of robotic gait training (RGT) and transcranial magnetic stimulation (TMS) initiated during inpatient rehabilitation and continued through early outpatient rehabilitation

CONDITIONS

Official Title

Dosing of Overground Robotic Gait Training with Functional Outcomes and Neuroplasticity After Spinal Cord Injury

Who Can Participate

Age: 16Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Motor incomplete spinal cord injury (traumatic or non-traumatic)
  • Acute or subacute phase of recovery
  • Medically stable as determined by a physician
  • Receiving medical care and rehabilitation at Baylor Scott & White Institute for Rehabilitation
  • All genders, races, and ethnicities
  • Meet frame limitations of the Ekso robotic exoskeleton device
  • Have continence or a program for bladder and bowel management
Not Eligible

You will not qualify if you...

  • Moderate to severe traumatic brain injury occurring at the same time
  • Degenerative diagnoses
  • Pre-existing developmental disability, significant psychological diagnosis, or other cognitive impairments
  • Pregnancy

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

Baylor Scott & White Institute for Rehabilitation

Dallas, Texas, United States, 75246

Actively Recruiting

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Research Team

F

Faith Meza, MPH

CONTACT

C

Christa Ochoa, MPH

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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