RECRUITING

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

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Conditions

Spinal Cord InjuriesExoskeletonWearable assistive technologyTranscranial magnetic stimulationRobotic gait training

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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

Official Title

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

Quick Facts

Study Start:2022-05-20
Study Completion:2026-09-14
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05218447

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:16 Years to 85 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:CHILD, ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * All types of motor incomplete SCI (traumatic and non-traumatic)
  2. * Acute/Subacute phase of recovery
  3. * Medically stable as deemed by physician
  4. * Undergoing medical care and rehabilitation at Baylor Scott \& White Institute for Rehabilitation
  5. * Both genders and all races and ethnicities
  6. * Meet the Ekso robotic exoskeleton frame limitations
  7. * Continence of or a program for bladder and bowel management
  1. * Concurrent moderate to severe traumatic brain injury (TBI)
  2. * Degenerative diagnoses
  3. * Pre-morbid developmental disability, significant psychological diagnosis, or other cognitive impairment
  4. * Primary residence \>90 miles away from Baylor Scott \& White Institute for Rehabilitation
  5. * Pregnancy

Contacts and Locations

Study Contact

Alexandria R Holden, MPH
CONTACT
469-531-1577
Alexandria.Holden@BSWHealth.org
Christa Ochoa, MPH
CONTACT
Christa.Ochoa@BSWHealth.org

Principal Investigator

Chad Swank, PhD, PT, NCS
PRINCIPAL_INVESTIGATOR
Baylor Research Institute

Study Locations (Sites)

Baylor Scott & White Institute for Rehabilitation
Dallas, Texas, 75246
United States

Collaborators and Investigators

Sponsor: Baylor Research Institute

  • Chad Swank, PhD, PT, NCS, PRINCIPAL_INVESTIGATOR, Baylor Research Institute

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-05-20
Study Completion Date2026-09-14

Study Record Updates

Study Start Date2022-05-20
Study Completion Date2026-09-14

Terms related to this study

Keywords Provided by Researchers

  • Exoskeleton
  • Wearable assistive technology
  • Transcranial magnetic stimulation
  • Robotic gait training

Additional Relevant MeSH Terms

  • Spinal Cord Injuries