Injuries, Spinal Cord Clinical Trial
Official title:
The WISE Trial - Walking Improvement for SCI With Exoskeleton
A randomized, controlled trial comparing exoskeleton gait training with standard gait training or no gait training in community-dwelling participants with chronic incomplete spinal cord injury
Community dwelling iSCI participants may improve clinical gait function by engaging in a gait training regimen, where robotic exoskeletons can readily deliver a precise dose and simultaneously reduce the physical stress imposed on therapists using conventional manually assisted stepping practice. Exoskeleton training is predicted to improve function in participants receiving usual care, but not superior to intensity-matched manual training. The rationale to implement exoskeleton robotics as preference in gait training is based on precision dosing, over-ground training, and reduced therapist burden for high repetition training. The investigators aim to demonstrate that Ekso exoskeleton training can significantly improve gait speed in stable chronic, community-dwelling incomplete SCI (iSCI) participants. The objectives of this study are the following: A. Primary Objective: To demonstrate that a 12 week robotic gait training regimen can lead to a clinically meaningful improvement in independent gait speed on the 10 Meter Walk Test (10MWT) in community dwelling participants with chronic iSCI. B. Secondary Objectives: 1. To examine the economic factors such as number of physical therapists/staff required during training. 2. To analyze the physical burden on therapists assisting and supervising during training. 3. To study the influence of factors that may modify the gait recovery in the chronic incomplete SCI population (demographic, clinical, functional, psychological, balance, etc.). ;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT04530955 -
Transitioning to a Valve-Gated Intrathecal Drug Delivery System (IDDS)
|
N/A | |
Completed |
NCT00654082 -
A Study Evaluating the Efficacy and Safety of Sildenafil in Men With Traumatic Spinal Cord Injury and Erectile Dysfunction
|
Phase 4 | |
Completed |
NCT01920243 -
Evaluation of a Bowel and Bladder Health Management Program for Individuals With Spinal Cord Injury (SCI)
|
N/A | |
Active, not recruiting |
NCT02917590 -
Dual-task Obstacle Crossing Training in Ambulatory Subjects With Spinal Cord Injury
|
N/A | |
Completed |
NCT02913911 -
Sit-to-stand With Feedback in SCI Patients
|
N/A | |
Completed |
NCT00252954 -
Levetiracetam in Chronic Neuropathic Pain Following Spinal Cord Injury
|
Phase 4 | |
Recruiting |
NCT02944669 -
ReWalk Personal Device Postmarket Study
|
N/A | |
Completed |
NCT02916784 -
Sit-to-stand in Spinal Cord Injury Patient
|
N/A | |
Recruiting |
NCT04460872 -
Locomotor Training With Testosterone to Promote Bone and Muscle Health After Spinal Cord Injury
|
Phase 2 | |
Completed |
NCT03914456 -
Assessment of Neurorehabilitation in Spinal Cord Injury Using Neuroimage Tools.
|
N/A | |
Completed |
NCT02556125 -
Diaphragm Pacing After Spinal Cord Injury
|
||
Completed |
NCT02274649 -
Clinical Trial to Evaluate One-to-one Peer Mentoring
|
N/A |