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Spinal Injuries clinical trials

View clinical trials related to Spinal Injuries.

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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: NCT02886260 Recruiting - Quality of Life Clinical Trials

Establishing a Descriptive Cohort of Patients Cared for Operation on the Spine

KEOPS
Start date: August 28, 2012
Phase:
Study type: Observational

This study aims to: 1. describe the monitoring of patients treated for spinal disorders. 2. create a comprehensive database of reliable and readily exploitable quickly to produce a library of cross publications between orthopedic surgery and neurosurgical services. This database will include clinical, functional , radiographic , educational, social and professional data. 3. obtain a cohort of patients in the comprehensive range of spinal pathologies. 4. standardize data collection in this cohort with similar national projects.

NCT ID: NCT02776930 Completed - Clinical trials for Musculoskeletal Injury

Predictive Models for Spine and Lower Extremity Injury After Discharge From Rehab

MP3-RD
Start date: March 2016
Phase:
Study type: Observational

The purpose of this study is to develop algorithms that will help predict future injury and/or re-injury after being returned to duty from a musculoskeletal injury. After completion of an episode of care with a physical therapist, the subjects will undergo a battery of physical performance tests and fill out associated surveys. The subjects will then be followed for a year to identify the occurrence/re-occurence of any injuries. Based on the performance on the physical evaluation tests, algorithms will be derived using regression analysis to predict injury. Subjects will be recruited from the pool of patients that have recently completed physical rehabilitation in physical therapy clinics for their lower extremity or lumbar/thoracic spine injury.

NCT ID: NCT02767427 Completed - Infection Clinical Trials

The Value of Home Chlorhexidine Pre-Surgical Wash Before Spine Surgery

Start date: February 2016
Phase: N/A
Study type: Interventional

The study team hypothesizes that at-home cleansing of the surgical site with chlorhexidine wipes provide no added benefit to decreasing microbial activity or preventing surgical site infections. Patients will be randomized to the chlorhexidine or no additional intervention groups. Patients will be randomized to use 4% chlorhexidine cloths, while the other half receive no additional intervention. Those randomized into the chlorhexidine gluconate (CHG) home-application group will be asked to shower the night before surgery, and to use a standardized pre-packaged CHG wipe (that the patients would receive at their pre-surgical consultation) on their surgical site after thoroughly drying those areas. The patients will be asked to use a second wipe in each area the morning of surgery. The surgical sites will be analyzed in two groups: anterior cervical and posterior spine. Each of these two groups will be randomized separately. All patients will undergo a standardized preoperative cleansing regimen. Once positioned, they will be cleansed with an alcohol solution. Then, the surgical site (either the anterior portion of the neck or the posterior area of the spine) will be scrubbed with chlorhexidine soaked brushes and then painted with chlorhexidine solution. Perioperative antibiotics will be given per attending surgeon preference. Cutaneous samples will be taken from the surgical site of each patient at each time point.

NCT ID: NCT02705690 Not yet recruiting - Clinical trials for Arthroplasty, Replacement, Knee

Benchmarking the iOS Balance Application Against the Berg Balance Test

BBAaBBT
Start date: May 2016
Phase: N/A
Study type: Interventional

This study aims to benchmark the performance of an iOS application against the Berg Balance Scale (BBS), which is the most commonly used assessment tool by clinicians for measuring balance across the continuum from acute care to community-based care. An iPhone will be tied around the waist of the participant and concurrent measurements will be taken for five of the fourteen stances which comprise the BBS.

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.