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Spinal Cord Injuries clinical trials

View clinical trials related to Spinal Cord Injuries.

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NCT ID: NCT05354206 Terminated - Clinical trials for Spinal Cord Injuries

Neural Facilitation of Movements in People With SCI

Start date: July 12, 2022
Phase: N/A
Study type: Interventional

Spinal cord injury leads to long-lasting paralysis and impairment. Re-enabling movement of paralyzed areas is challenging and more information is needed about neurological recovery. The purpose of this study is to understand the contribution of individual neural tracts to movements facilitated by transcutaneous spinal cord stimulation (SCS).

NCT ID: NCT04854057 Terminated - Clinical trials for Spinal Cord Injuries

Pairing Intermittent Hypoxia and Transcutaneous Electrical Spinal Cord Stimulation to Promote Arm Use After Cervical SCI

Start date: March 3, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to test the efficacy of mild breathing bouts of low oxygen (intermittent hypoxia) combined with transcutaneous electrical spinal cord stimulation on restoring hand function in persons with chronic incomplete spinal cord injury.

NCT ID: NCT04818814 Terminated - Chronic Pain Clinical Trials

SCI Pain App Intervention Study

Start date: October 4, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to find out if using an app is a feasible and acceptable treatment for chronic pain in persons with spinal cord injury. Participants will have a 50% chance of being asked to listen to 10 minutes of audio-guided meditations using an app each day for six weeks, and a 50% chance of being asked to listen to 10 minutes of engaging and distracting presentations about topics of interest to the individual (TED Talks) for six weeks. All participants will be asked to complete three online surveys about their emotional and physical health lasting 20-30 minutes (one when the participant first enters the study, one six weeks later, and another six weeks later). Additionally, participants will be asked to complete brief (<5 minute) online surveys once a week during the first six weeks of their participation. Participation in this study is very low risk, and participants may not experience any personal benefit from their participation. Participation in this study is entirely voluntary.

NCT ID: NCT04586777 Terminated - Clinical trials for Spinal Cord Injuries

Effects of Transvertebral Direct Current Stimulation in Humans

Start date: January 15, 2014
Phase: N/A
Study type: Interventional

This study will evaluate the effects of non-invasive stimulation of the spinal cord in people with spinal cord injury.

NCT ID: NCT04581525 Terminated - Clinical trials for Spinal Cord Injuries

Modulating Neuropathic Pain With Transcranial Direct Current Stimulation

Start date: June 7, 2012
Phase: N/A
Study type: Interventional

This study will examine whether a form of non-invasive brain stimulation can help reduce pain in people with persistent neuropathic pain.

NCT ID: NCT04367623 Terminated - Clinical trials for Spinal Cord Injuries

Motor Conditioning to Enhance the Effect of Physical Therapy

Start date: December 9, 2020
Phase: N/A
Study type: Interventional

Spinal Cord Injury (SCI) affects person's ability to move and feel sensation from the body. About half of patients with tetraplegia (high level SCI) have an incomplete injury, i.e. have some sensation and control of muscles preserved and could recover some function of their upper limbs. In this study the researchers would like to increase the effect of physical therapy of the upper limbs by sensory-motor priming. To achieve this they will use Brain Computer Interface (BCI) controlled Functional Electrical Stimulation (FES) immediately prior to the physical therapy of the upper limbs. BCI will be operated by motor attempt (motor priming) which will activate the FES applied to participants' hand muscles to achieve movement (sensory and motor priming). Physical therapy in this study will not replace conventional therapy that participant receive as a part of their standard treatment. There will be two groups: a treatment group (BCI FES with physical therapy) and a control group (physical therapy only), each receiving 20 therapy sessions of matched duration (40-50 min) of their dominant hand. Based on power analysis and results from our study (Osuagwu et al. 2016, J Neural Eng) there will be thirteen participants per group matched by age and the level of injury. Therapy will be applied to dominant hand only, because of the limited time available for experimental studies on participants who are already under active rehabilitation programme. Primary measures will be functional outcomes (range of movement, muscle strength, grip force, independence) while secondary outcomes will be neurological outcomes (EEG activity) and quality of life measures. The outcomes will be compared between the treatment and the control group and between the dominant and the non-dominant hand of each participant.

NCT ID: NCT04319679 Terminated - Pain Clinical Trials

ESWT for UE Pain in Patients With Cervical Spinal Cord Injury

Start date: June 5, 2020
Phase: N/A
Study type: Interventional

This study aimed to investigate the efficacy and safety of extracorporeal shockwave therapy (ESWT) for upper extremity pain related to spasticity in patients with spinal cord injury.

NCT ID: NCT04265560 Terminated - Clinical trials for Spinal Cord Injuries

Progressive Resistance Training in Acute Spinal Cord Injury

Start date: November 1, 2019
Phase: N/A
Study type: Interventional

Muscle weakness is one of the most common and debilitating symptoms following a Spinal Cord Injury (SCI). Strength training is recommended as an effective means to increase muscular strength and improve function for individuals with long term SCI. In contrast, the strength training guidance for those with a recent (<1 year) SCI is lacking. Therefore, this study aims to investigate the feasibility of a method of upper limb strengthening - Progressive Resistance Training (PRT) and its impact upon muscle strength and function.

NCT ID: NCT04238013 Terminated - Clinical trials for Spinal Cord Injuries

Neuromodulation of Ankle Muscles in Persons With SCI

Start date: July 6, 2021
Phase: N/A
Study type: Interventional

The ability to voluntarily move the ankles is important for walking. After spinal cord injury (SCI), this ability is impaired because of changes in the communication between the brain, spinal cord, and body. Whole body vibration (WBV) is a treatment that increases voluntary muscle control and decreases uncontrollable muscle movement in people with SCI. The purpose of this study is to understand how WBV can impact ankle control and uncontrollable muscle movement.

NCT ID: NCT04217577 Terminated - Clinical trials for Spinal Cord Injuries

Dried Plum Supplementation as Treatment for Bone Loss Following Spinal Cord Injury

Start date: January 20, 2019
Phase: N/A
Study type: Interventional

The purpose of this pilot study is to explore whether dried plum (prunes) added to the diet is effective in reducing or reversing bone loss following spinal cord injury (SCI). The investigators will look for changes in bone mineral density as well as evidence in the blood of markers of bone activity. The first part of the study is to check whether participants with SCI can and will eat the required amount of dried plums (prunes) on a daily basis. The second part of the study is to follow participants over one year and look for changes in bone mass and blood markers.