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Cerebral Palsy clinical trials

View clinical trials related to Cerebral Palsy.

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NCT ID: NCT00338871 Completed - Cerebral Palsy Clinical Trials

Home Based Exercise Program for Brain Injury Children

Start date: June 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to examine whether simple home-base aerobic exercise program have beneficial effect on walking abilities and balance performance in children with brain damage

NCT ID: NCT00338858 Completed - Cerebral Palsy Clinical Trials

The Connection Between Gait Variability Parameters and Balance Performance in Children With Physical Disability

Start date: June 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to explore the connection between gait variability parameters and balance performance in children with physical disability

NCT ID: NCT00337688 Completed - Cerebral Palsy Clinical Trials

Power Wheelchair Joystick Use in Spastic Cerebral Palsy

Start date: July 2006
Phase: N/A
Study type: Observational

There are over 750,000 individuals in the U.S. with Cerebral Palsy (CP). Up to 46% of adults with CP report limited mobility in their communities. However, upper limb spasticity and problems with movement can make the independent use of a wheelchair difficult. Forty percent of individuals who desire mobility via electric wheelchairs are precluded from using them because of problems with upper limb function. No studies to date have produced devices that definitively improve mobility for these individuals. We will recruit 22 subjects with Spastic CP and 22 age and gender matched control subjects without apparent disability from advertisements, mailings, and outpatient clinics. Both a conventional joystick (MSJ) and a novel joystick that is customized for each subject will each be used six different computer screen tasks that simulate driving a wheelchair on a path. We will compare subjects and joysticks based on driving performance. Understanding problems with driving will help us to design joysticks and other assistive devices, not only for CP but for Traumatic Brain Injury, Spinal Cord Injury, Parkinson's Disease, stroke, or a variety of other disabilities.

NCT ID: NCT00306761 Completed - Clinical trials for Cerebral Palsy, Spastic

Effects of Dynamic Wheelchair Seating on Spasticity and Functional Mobility in Children

Start date: April 2006
Phase: N/A
Study type: Interventional

Cerebral palsy (CP) is a non-degenerative neuromuscular disease that can exist at or occur as a result of birth. Because of damage to one or more parts of the brain that control movement, an affected child cannot control his or her muscles normally. Prevalence of CP is similar worldwide, with pronounced severity in underdeveloped countries due to poor health and financial conditions. Research should be conducted to find methods of medical treatment to allow affected children to maintain or regain musculoskeletal functionality. Many children affected with CP spend much of their days restricted to a rigid wheelchair; limiting muscular and cognitive development, making it difficult to interact with their environment. The gap to be addressed by this study is to determine if a wheelchair that is based on the dynamics of human anatomy can allow enhanced function, while being adaptive to individual growth and development. At present, there is very little dynamic capability available in commercial wheelchairs to allow this mobility. A dynamic wheelchair system was recently designed and a small sample of able-bodied children has been tested in the chair. It is hypothesized that significant increases in functional mobility will be achieved in children with CP from the use of this novel wheelchair design.

NCT ID: NCT00305006 Completed - Cerebral Palsy Clinical Trials

Constraint-induced Movement Therapy (CIMT) and Bimanual Training (HABIT) in Children With Hemiplegic Cerebral Palsy

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

A randomized control trial of bimanual training. The protocols have been developed at Columbia University to be child friendly and draws upon our experience since 1997 with constraint-induced movement therapy in children with cerebral palsy.

NCT ID: NCT00295295 Completed - Cerebral Palsy Clinical Trials

Vibration Intervention to Improve Bone and Muscle in Children With Cerebral Palsy

Start date: September 2004
Phase: Phase 2
Study type: Interventional

Cerebral palsy is a group of disorders characterized by lack of coordination in the muscles, loss of movement, and speech disturbances. These disorders are caused by injuries to the brain that occur during fetal development or near the time of birth. The purpose of this study is to determine the effects of high frequency, low magnitude vibration on bone and muscle in children with cerebral palsy.

NCT ID: NCT00292786 Completed - Cerebral Palsy Clinical Trials

The Effects of Electrical Stimulation Gait Training on Walking and Posture for Children With Cerebral Palsy

Start date: June 2005
Phase: N/A
Study type: Interventional

This proposal is designed to achieve the following specific aims and will test the associated hypotheses: AIM 1: To compare walking ability, standing posture, gait initiation and functional standing and stepping of twenty children with typical development to that of twenty children with spastic diplegia or hemiplegia, CP. Hypotheses - Children with CP will demonstrate impaired coordination as compared to children of typical development. In addition, children with CP will demonstrate inappropriate foot contact area, decreased velocity and step length as compared to children of typical development. - Children with CP will demonstrate impaired postural control as compared to children of typical development. - Children with CP will demonstrate an impaired gait initiation motor program as compared to children with typical development. - Children with CP will take more time to complete the timed up and go test and demonstrate decreased reaching distances in the functional reach test as compared to children of typical development. AIM 2: Using a single-blinded, randomized, controlled study design, to assess the ability of a 12-week at-home electrical stimulation gait training program to improve walking ability, standing posture, gait initiation, functional standing and stepping, and satisfaction with walking ability for a group of 10 children with spastic diplegia or hemiplegia CP as compared to a group of 10 children with spastic diplegia or hemiplegia CP who undergo a 12-week at-home gait training program without electrical stimulation. Hypotheses - The ES gait training group will demonstrate improved joint coordination as compared to the group undergoing a gait training program without ES. The ES gait training group will demonstrate improved foot contact area, increased self-selected walking velocity and greater step length as compared to the group undergoing a gait training program without ES. - The ES gait training group will demonstrate improved postural control as compared to the group undergoing a gait training program without ES. - The ES gait training group will demonstrate improved gait initiation as compared to the gait training group without ES. - The ES gait training group will demonstrate decreased times on the Timed Up and Go and an increase in functional reach as compared to the group undergoing a gait training program without ES. - The ES gait training group will demonstrate greater satisfaction and self-perceived performance on everyday tasks related to walking function and posture as measured by the COPM compared to the group that undergoes a gait training program without ES.

NCT ID: NCT00281359 Completed - Cerebral Palsy Clinical Trials

A Comparative Study of the Effectiveness of Treatment of Contractures With Mechanically Applied Stretch and Heat.

Start date: April 2003
Phase: N/A
Study type: Interventional

This study is looking at new ways to stretch knee contractures in children with cerebral palsy using a specially designed splint.

NCT ID: NCT00261131 Completed - Clinical trials for Spastic Diplegic Cerebral Palsy

Efficacy and Functional Outcomes of Botulinum Toxin A Injections to Hamstrings in Flexed Knee Gait in Cerebral Palsy

Start date: March 2006
Phase: Phase 3
Study type: Interventional

The study proposes to determine if injections of BTX-A to the hamstring muscles result in measurable physiologic changes not observed with normal saline injections in children with spastic diplegic cerebral palsy who walk with a flexed-knee gait pattern.

NCT ID: NCT00255073 Completed - Clinical trials for Spastic Diplegic Cerebral Palsy

Does Reducing Spasticity Permit an Increase in Strength?

Start date: January 2005
Phase: Phase 2
Study type: Interventional

Reduction of spasticity has been a major focus of the treatment of childhood cerebral palsy, resulting in numerous treatment strategies that target various parts of the motor system. However, in many children weakness may be a greater contributor to disability than spasticity. Recent results suggest a correlation between spasticity and weakness, but it is not known if reduction of spasticity can improve strength. We suggest a simplified model in which spinal mechanisms (including reflex contributions to spasticity) and supraspinal mechanisms (including voluntary contributions to strength) combine to activate muscle. The model implies that the supraspinal contribution cannot increase unless the spinal contribution decreases. We therefore hypothesize that reduction of spasticity improves the ability to increase voluntary strength. We propose a double-masked placebo-controlled clinical trial combining treatment using the oral anti-spasticity medication baclofen with a 6-week program of strength training. We will enroll 20 ambulatory children with spastic diplegic cerebral palsy. Prior to and following the intervention, we will obtain quantitative measures of spasticity, strength, and gait. We predict that the children taking baclofen will have a greater increase in strength than the children taking placebo. We predict that the increase in strength will be reflected in improved performance on gait analysis, and it will correlate with a reduction in quantitative measures of spasticity and spinal reflex excitability. If the hypothesis is correct, it will provide important new information on the relationship between spasticity and strength in children with cerebral palsy. It will provide the first measurements of the effect of baclofen on voluntary muscle activation in children. It will support the short-term use of combined anti-spasticity medication and strengthening as a new clinical treatment for ankle weakness in children with spastic diplegia. A successful result will have immediate and significant implications for treatment of children with cerebral palsy.