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Paralysis clinical trials

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NCT ID: NCT01923662 Completed - Spinal Cord Injury Clinical Trials

A Neuroprosthesis for Prolonged Standing After SCI Using Multi-Contact Peripheral Nerve Electrodes

Start date: April 11, 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to improve the performance of neuroprosthesis for standing after SCI by developing and testing new advanced methods that use multiple contact peripheral nerve electrodes to slow the onset of fatigue and increase standing duration. The new advanced methods will take advantage of the ability of multiple-contact nerve cuff electrodes to selectively activate portions of a muscle that perform the same action. Alternating activation to multiple muscles (or parts of the same muscle) rather than continuously activation the entire muscle group constantly should allow them to rest and recover from fatiguing contractions. This should allow users to remain upright for longer periods of time to perform activities of daily living, reduce the risk of falls due to fatigue, and increase the potential of receiving the health benefits of standing.

NCT ID: NCT01906424 Completed - Spinal Cord Injury Clinical Trials

Restoring Arm and Hand Function With Non-invasive Spinal Stimulation

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

This study is to determine if non-invasive electrical stimulation of the spinal cord can help improve hand and arm function in people with paralysis who suffered a cervical spinal cord injury.

NCT ID: NCT01905683 Completed - Clinical trials for Lower Limb and Combined Lower Limb and Upper Limb Spasticity Due to Cerebral Palsy

Long-term Open-label Study of Botulinumtoxin Type A to Treat Spasticity of Leg(s) or Leg(s) and Arm in Cerebral Palsy

Start date: August 2013
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether injections of Botulinum toxin type A into muscles of the leg(s) or of leg(s) and one arm are safe in treating children/adolescents (age 2-17 years) long-term with increased muscle tension/uncontrollable muscle stiffness (spasticity) due to cerebral palsy.

NCT ID: NCT01903603 Completed - Cerebral Palsy Clinical Trials

A Longitudinal Study of Movement and Participation in Patients With Cerebral Palsy

Start date: August 2012
Phase: N/A
Study type: Observational

The primary goal of this study is to establish and evaluate an image-based biomarker for the impaired motor control and sensory information processing present in Cerebral palsy (CP) patients

NCT ID: NCT01901211 Completed - Cerebral Palsy Clinical Trials

Physical and Social Benefits of Multi-Player Interactive Computer Play Games in Youth With Cerebral Palsy

Start date: September 2013
Phase: N/A
Study type: Interventional

As children with cerebral palsy (CP) become teenagers, they experience a decrease in their physical function and mobility. Decreased mobility leads to increased social isolation for the teens and impacts negatively on their quality of life. This loss of function is multifactorial, but poor physical fitness and muscle weakness secondary to disuse are significant contributors. Exercise video games are a novel approach to engage youth in physical exercise and social interaction with their peers. The objective of this study is to evaluate the impact of an exercise video gaming intervention to improve physical fitness and social wellbeing. Our over-arching research questions are whether "exergames" can provide health benefits (improved physical fitness) and improved social wellbeing in youth with CP.

NCT ID: NCT01872507 Completed - Cerebral Palsy Clinical Trials

BioFeedBack Breathing Training Influence Cardiac Autonomic Nervous System in Children With Cerebral-Palsy.

Start date: July 2013
Phase: N/A
Study type: Interventional

The effect of breathing biofeedback training to influence the function of the cardiac autonomic nervous system at rest and in activity in children with cerebral palsy. Cerebral palsy children suffer from a non-progressive damage of the brain. It is the most common injury that causes physical handicapped in childhood. There are a few researches that investigated the autonomic function in cerebral palsy children. Those researches found hyperactivity of the sympathetic autonomic system, including high resting heart rate compare to their typically developed pears. The recommended treatment for cerebral palsy is activity, muscle strengthening and mobility. The impairment in the autonomic system influences the everyday function and has correlation with secondary morbidity. As far as we know there are no researches who investigated the following issues. In this study we would like to: 1. Describe the autonomic cardiac function, Breathing function, motor function and the correlation between them in children with cerebral palsy. 2. Compare the autonomic cardiac function at rest in aerobic test and in diaphragmatic breathing. 3. Test the influence of breathing training on Heart rate variability parameters at rest, in aerobic test right after the breathing training program and one month after, in children with cerebral palsy

NCT ID: NCT01860196 Completed - Clinical trials for Adult Cerebral Palsy

Efficacy and Safety of Meditoxin® Injection for Cervical Dystonia in Adults With Cerebral Palsy

ATHETOID_CD
Start date: June 2013
Phase: Phase 4
Study type: Interventional

This study aimed to compare the efficacy and safety of Meditoxin® injection for cervical dystonia in adults with cerebral palsy. It is a placebo controlled, Cross-over, Double blind, Randomized, Clinical trial.

NCT ID: NCT01840930 Recruiting - Clinical trials for Orthopedic Complications in Cerebral Palsy

Cohort of Children With Severe Cerebral Palsy

CPCohort
Start date: September 2009
Phase:
Study type: Observational

" Cohort CP " is a multicentre cohort study, initiated by the Hospices Civils de Lyon in September 2009. Population targeted are children with bilateral cerebral palsy, level GMFCS IV or V, aged from 2 to 10 years at inclusion. They are followed-up during 10 years, at the rhythm of 1 visit per year. At each visit are collected clinical, orthopaedic, radiological and environmental data. The primary objective is to establish the incidence of orthopaedic complications (scoliosis and hip joint) depending on patients' age. Secondary objectives are to describe the sequences over time of these complications and the related pain, to explore the impact of nutrition, surgery, asymmetric postures and environmental factors, and to describe the medical and rehabilitative follow-up of these patients. 385 patients are expected by the end of 2020. We expect of this long-term follow-up to gain tools that permit to improve patient's care and patient's quality of life, by putting in place preventing actions and adapted treatments related to their own pathologies.

NCT ID: NCT01824849 Completed - Airway Obstruction Clinical Trials

Total Versus Partial Arytenoidectomy in Bilateral Vocal Fold Paralysis

Start date: January 2011
Phase: N/A
Study type: Interventional

Total arytenoidectomy is claimed to increase risk of aspiration and cause more voice loss than other operations performed for bilateral vocal fold paralysis (BVFP). However, objective evidence for such conclusion is lacking. There is no study comparing swallowing and voice after total and partial arytenoidectomy.

NCT ID: NCT01806233 Recruiting - Ischemic Stroke Clinical Trials

Lu's Acupuncture and Moxibustion Treatment on Stroke

LAMTS
Start date: March 2013
Phase: N/A
Study type: Interventional

There will be successive changes in traditional Chinese medicine rehabilitation for stroke patients with limb hemiparetic through therapy of acupuncture and moxibustion.