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Injuries, Spinal Cord clinical trials

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NCT ID: NCT04530955 Recruiting - Clinical trials for Traumatic Brain Injury

Transitioning to a Valve-Gated Intrathecal Drug Delivery System (IDDS)

Start date: September 24, 2020
Phase: N/A
Study type: Interventional

Comparing the efficacy of Intracthecal Baclofen dose between the Prometra II and Medtronic SynchroMed II for patients with spasticity and with current a current SyncroMed II pump needing replacement.

NCT ID: NCT04460872 Recruiting - Clinical trials for Spinal Cord Injuries

Locomotor Training With Testosterone to Promote Bone and Muscle Health After Spinal Cord Injury

Start date: January 31, 2021
Phase: Phase 2
Study type: Interventional

This pilot study will determine the feasibility of implementing a combinatory rehabilitation strategy involving testosterone replacement therapy (TRT) with locomotor training (LT; walking on a treadmill with assistance and overground walking) in men with testosterone deficiency and walking dysfunction after incomplete or complete spinal cord injury. The investigators hypothesize that LT+TRT treatment will improve muscle size and bone mineral density in men with low T and ambulatory dysfunction after incomplete or complete SCI, along with muscle fundtion and walking recovery in men with T low and ambulatory dysfunction ater incomplete SCI.

NCT ID: NCT03914456 Completed - Clinical trials for Injuries, Spinal Cord

Assessment of Neurorehabilitation in Spinal Cord Injury Using Neuroimage Tools.

Start date: February 2, 2007
Phase: N/A
Study type: Interventional

The sensorimotor cortex may play a role in the functional recovery after Spinal Cord Injury (SCI) through efference generated in the absence of the afference. OBJECTIVE: The purpose of this study was to evaluate the potential reorganization in the sensorimotor cortex in SCI patients after Body Weight Supported Treadmill Training (BWSTT) associated with conventional motor rehabilitation. METHOD: Seven SCI patients with ASIA C and D participated in this study. They were submitted to a motor-task functional magnetic resonance imaging study (fMRI) before and after the rehabilitation treatment.

NCT ID: NCT02944669 Recruiting - Clinical trials for Injuries, Spinal Cord

ReWalk Personal Device Postmarket Study

Start date: June 2016
Phase: N/A
Study type: Observational

This study seeks to further evaluate the Multi-Tiered Training Program and to further explore the overall safety profile of the ReWalk Personal Device outside of the institutional setting under conditions of routine medical practice.

NCT ID: NCT02943915 Completed - Clinical trials for Injuries, Spinal Cord

The WISE Trial - Walking Improvement for SCI With Exoskeleton

WISE
Start date: September 2016
Phase: N/A
Study type: Interventional

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

NCT ID: NCT02917590 Active, not recruiting - Clinical trials for Injuries, Spinal Cord

Dual-task Obstacle Crossing Training in Ambulatory Subjects With Spinal Cord Injury

Start date: October 2015
Phase: N/A
Study type: Interventional

Is dual-task obstacle crossing training more efficiently than single-task obstacle crossing training on the improvement of walking ability, balance ability, and lower extremity muscle strength in ambulatory subjects with spinal cord injury

NCT ID: NCT02916784 Completed - Clinical trials for Injuries, Spinal Cord

Sit-to-stand in Spinal Cord Injury Patient

Start date: July 2015
Phase: N/A
Study type: Observational

1. Were there differences in functional ability between ambulatory individuals with SCI who passed and failed the independent sit-to-stand (iSTS) task? 2. Did the ability of iSTS relate to ability of walking as determined using a type of AAD used? 3. What were factors associated with the ability of iSTS?

NCT ID: NCT02913911 Completed - Clinical trials for Injuries, Spinal Cord

Sit-to-stand With Feedback in SCI Patients

Start date: November 2015
Phase: N/A
Study type: Interventional

- Does the utility of external feedback in terms of goal-directed LLL approach during STS training immediately improve functional ability relating to walking in ambulatory patients with SCI? - Does the utility of LLL feedback improve functional ability relating to walking in ambulatory patients with SCI after 2-week training?

NCT ID: NCT02556125 Completed - Clinical trials for Injuries, Spinal Cord

Diaphragm Pacing After Spinal Cord Injury

Start date: December 2015
Phase:
Study type: Observational

Respiratory dysfunction is the leading cause of death in individuals with spinal cord injuries (SCIs). Nearly one quarter of all SCI cases involve injury to the upper spinal cord segments which impairs neural activation of the diaphragm muscle and compromises breathing. Although mechanical ventilation can be life-saving after cervical SCI (C-SCI), it also triggers rapid and profound diaphragm muscle atrophy, thereby complicating (or even preventing) ventilator weaning. Intramuscular diaphragm stimulation, or diaphragm pacing, was developed to replace long-term ventilator support, and is now used acutely post C-SCI (<4 months following injury) to promote ventilator weaning. The impact of diaphragm pacing on respiratory function and diaphragm muscle activation has not been formally evaluated. This is an essential step in determining the efficacy of intramuscular diaphragm stimulation and its effects on respiratory function after SCI. Accordingly, this research study will evaluate the effects of intramuscular diaphragm stimulation and test the hypothesis that diaphragm pacing enhances neuromuscular diaphragm activation and respiratory function in adults with cervical SCIs. The investigators will test the hypothesis by evaluating the effects of diaphragm pacing on neuromuscular activation of the diaphragm by directly recording electromyogram (EMG) activity from the intramuscular pacing electrodes. Recording from these surgically-implanted electrodes allows direct comparisons of EMG activity across time, minimizing methodological limitations inherent with surface or percutaneous EMG recordings. This approach, in association with respiratory assessments, will be used to investigate the impact of diaphragm pacing in adults with intramuscular diaphragm pacing electrodes following acute, traumatic C-SCIs.

NCT ID: NCT02274649 Completed - Clinical trials for Injuries, Spinal Cord

Clinical Trial to Evaluate One-to-one Peer Mentoring

Start date: April 2014
Phase: N/A
Study type: Interventional

The research will examine the effects of enhanced peer mentor interactions on facilitating a successful transition to community living following traumatic spinal cord injury (SCI). Participants in the research will be assigned to either (1) the control group that will receive traditional peer mentor types of interactions or (2) to the intervention group that will receive an enhanced peer mentor program called the One-on-One Initiative. Assignment to one of these two groups will occur randomly on admission to Shepherd Center; the only stratifying criteria is injury level - C6 and above vs. C7 and below.