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Injuries, Spinal Cord clinical trials

View clinical trials related to Injuries, Spinal Cord.

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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: 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: 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.

NCT ID: NCT01920243 Completed - Clinical trials for Urinary Bladder, Neurogenic

Evaluation of a Bowel and Bladder Health Management Program for Individuals With Spinal Cord Injury (SCI)

Start date: October 28, 2013
Phase: N/A
Study type: Interventional

This study will look at the use of a telehealth version of a self management program in individuals with both new onset and chronic traumatic spinal cord injuries. The program is called Health Mechanics. It is meant to enhance self management skills related to neurogenic bladder and bowel management to prevent associated problems and improve Quality of Life (QOL). This program is based on the needs and strengths of individuals with SCI. It focuses on enhancing skills, encouraging positive health behaviors, empowering people within their own environments, and recognizing that people differ in their resources and abilities. The skills that are part of the intervention are: attitude, self-monitoring, problem-solving, communication, organization and stress management. This study will address those skills in the context of bladder and bowel health, with expectations that these skills to be useful in other areas of life as well. The investigators hypothesize that individuals in the Health Mechanics intervention group will: - show greater improvements in problem solving skills, healthy attitudes about disability and knowledge of SCI management skills than will the control group - have greater adherence to recommended bladder and bowel management behaviors than the control group - have fewer bladder and bowel complications than the control group - have higher levels of QOL than the control group In other words, this study will investigate the effectiveness of a telehealth version of Health Mechanics to enhance self-management skills related to neurogenic bladder and bowel management in an attempt to prevent associated complications and improve QOL.

NCT ID: NCT00654082 Completed - Spinal Cord Injury Clinical Trials

A Study Evaluating the Efficacy and Safety of Sildenafil in Men With Traumatic Spinal Cord Injury and Erectile Dysfunction

Start date: September 2002
Phase: Phase 4
Study type: Interventional

To demonstrate the efficacy, safety and tolerability of sildenafil administered orally, as required, approximately 1 hour prior to sexual activity to men with erectile dysfunction (ED) associated with spinal cord injury (SCI), as well as its effects on the quality of life (QoL) of these patients.

NCT ID: NCT00252954 Completed - Pain Clinical Trials

Levetiracetam in Chronic Neuropathic Pain Following Spinal Cord Injury

Start date: November 2005
Phase: Phase 4
Study type: Interventional

Purpose: To evaluate the efficacy and safety of levetiracetam on chronic neuropathic pain after spinal cord injury, and to examine its effect on spasms and evoked pain.