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Spinal Cord Injuries clinical trials

View clinical trials related to Spinal Cord Injuries.

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NCT ID: NCT00995215 Completed - Clinical trials for Spinal Cord Injuries

Sub-study to Spinal Cord Stimulation to Restore Cough

Start date: October 2009
Phase: N/A
Study type: Interventional

Evaluation of Wire Electrodes to Activate the Expiratory Muscles to Restore Cough

NCT ID: NCT00990093 Completed - Clinical trials for Spinal Cord Injuries

A Randomised, Cross-over, Open-labelled Test Catheter Acceptance Study

Start date: November 2009
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate that the test catheter is no less accepted than the SpeediCath (SC) catheter.

NCT ID: NCT00987155 Completed - Clinical trials for Cardiovascular Disease

Spinal Cord Injury: Endurance, Strength and Cardiac Function Induced by Efficient Training Protocols

Start date: January 2007
Phase: N/A
Study type: Interventional

1. Measurements of peak oxygen uptake (VO2peak) during passive leg cycling (PLC) combined with arm crank ergometry (ACE), leg vascular occlusion (100mmHg above systolic BP) combined with ACE, and FES isometric contractions combined with ACE in spinal cord injured (SCI). All the above mentioned parameters will be compared to Functional Electrical Stimulated (FES) lower extremity cycling combined with ACE (FEShybrid). The hypothesis is that VO2peak is significantly higher during FES hybrid cycling when compared to peak and submaximal PLC, leg vascular occlusion and ACE. But the values for VO2peak during FES isometric contractions combined with ACE is not significantly different from FES hybrid cycling. 2. Comparison of sub-maximal and peak VO2 values during arm crank (ACE) and wheelchair ergometry (WCE) in persons with spinal cord injury. The hypothesis is that wheelchair propulsion due to higher energy expenditure show higher work output and VO2peak than ACE. 3. Does 6 weeks of maximal strength training improve SCI subjects performance during WCE? WCE after 6 weeks maximal strength training is less strenuous owing to better work economy/ efficiency. 4. Effect from aerobic high intensity hybrid training on stroke volume (SV) and VO2peak in spinal cord injured men. 8 weeks of high intensity 4 times 4 interval training at 85-90% of peak heart rate during hybrid cycling. Hypothesis; VO2peak and SV will be significantly increased from training.

NCT ID: NCT00980434 Completed - Spinal Cord Injury Clinical Trials

S-100B and Neuron-specific Enolase (NSE) in Spinal Trauma

WBS
Start date: February 2008
Phase: N/A
Study type: Observational

The investigators are studying the clinical worth of the serum markers S-100B and NSE in patients with spinal cord injuries e.g. in patients with vertebral fractures. If there is a injury to the neuronal structures these two proteins could be secreted into the serum and add evidence to the severity of the injury.

NCT ID: NCT00977041 Completed - Pain Clinical Trials

Neurofeedback Treatment of Pain in Persons With Spinal Cord Injury (SCI)

Start date: August 2010
Phase: Phase 2
Study type: Interventional

A number of studies suggest that training to increase different types of brain waves is related to pain relief. The purpose of the second phase of this study is to see if neurofeedback training might help people with chronic pain control their pain better. The information from the study may help the investigators treat chronic pain better in the future.

NCT ID: NCT00951509 Completed - Spinal Cord Injury Clinical Trials

Virtual Reality Based Testing of Power Wheelchair Driving Skills

Start date: August 2011
Phase: N/A
Study type: Observational

The purpose of this research study is to examine whether computer based or virtual reality based driving assessments are as useful as real-world power wheelchair driving tests in measuring driving performance and whether they may be useful in helping to identify the problems that some individuals may have with driving power wheelchairs. The specific aims are as follows: Specific Aim 1: To develop computer-based and VR-based wheelchair driving assessments for both drivers and non-drivers that correspond to an accepted real-world driving assessment (Power Mobility Road Test) and compare them to the real-world assessment and to each other. Specific Aim 2: To develop additional features of the computer-based and VR-based assessments that present dynamic tasks and determine whether skills on these tasks can be delineated within the virtual environment.

NCT ID: NCT00947999 Completed - Pain Clinical Trials

Neurofeedback Treatment of Pain in Persons With Spinal Cord Injury (SCI)

Start date: July 2009
Phase: N/A
Study type: Observational

There has been little research on how chronic pain is related to brain activity. The purpose of this study is to learn more about pain and brain activity by finding any differences in brain activity among people who have moderate to severe chronic pain and a spinal cord injury, those who have a spinal cord injury but do not experience chronic pain, and people who have neither a spinal cord injury nor chronic pain (please note: subjects do not have to have pain to participate in this study). The information we collect will help the investigators get a better understanding of chronic pain.

NCT ID: NCT00947232 Completed - Multiple Sclerosis Clinical Trials

Motivational Interviewing to Increase Physical Activity to Treat Depression in People Aging With MS or SCI

inMotion
Start date: October 2009
Phase: N/A
Study type: Interventional

This study compares two approaches to helping people who are aging with MS or SCI and are experiencing depressed mood to become more physically active. The study is carried out entirely by telephone. There is no need to travel and participants may reside anywhere within the United States. We will examine the effects of the intervention on overall physical activity, mood, pain, fatigue and general health. Participants will complete surveys over the phone throughout the study and wear an activity monitor 3 times. The study is 6 months in length and participants may receive up to $120 for their time and effort.

NCT ID: NCT00919581 Completed - Spinal Cord Injury Clinical Trials

Pilot Study: The Role of Macrophage Migration Inhibitory Factor (MIF) in Spinal Cord Injury

Start date: May 2009
Phase: N/A
Study type: Observational

The purpose of the study is to investigate inflammatory and other substances that may be elevated in the blood and blood cells following spinal cord injury (SCI). These substances will be evaluated in samples from people who have had a spinal cord injury due to trauma (e.g. car accident or a fall) within the first week (acute) or at least one year ago (chronic). Specifically, the study will evaluate the presence and levels of a protein, macrophage migration inhibitory factor (MIF). MIF is released by cells and has a specific effect on the way cells behave, communicate and work together. In several other medical conditions, MIF is known to increase inflammation in the body. By comparing blood samples from individuals with spinal cord injury and uninjured (no spinal cord injury) individuals, the investigators will try to find out if MIF levels are increased in people with SCI. Investigators will also use these samples to measure other proteins that increase inflammation in the body and to see if the biological activities of MIF can be reduced in a test tube by adding other substances to the blood samples. It is hoped that this study of MIF and other proteins related to inflammation will help improve the treatment of SCI in the future. We hope to enroll a total of 312 subjects in this study (50 with acute spinal cord injury, 125 with chronic spinal cord injury, and 137 uninjured individuals).

NCT ID: NCT00890916 Completed - Spinal Cord Injury Clinical Trials

Hand Function for Tetraplegia

Start date: January 1, 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effectiveness of an implanted stimulator for providing hand function to individuals with cervical level spinal cord injury. The device stimulates the paralyzed muscles of the hand and forearm. The user of the device controls the stimulation by moving muscles that are not paralyzed, such as a wrist or neck muscle. The ability of the user to pick up and move objects, as well as perform various activities such as eating, drinking, and writing.