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Cerebral Palsy clinical trials

View clinical trials related to Cerebral Palsy.

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NCT ID: NCT03005249 Recruiting - Cerebral Palsy Clinical Trials

Neural Stem Cells Therapy for Cerebral Palsy

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

To evaluate the safety and efficacy of neural stem cells (NSCs) therapy for cerebral palsy.

NCT ID: NCT03003026 Completed - Cerebral Palsy Clinical Trials

Bike Skills Training for Children With Cerebral Palsy

CPBIKERCT
Start date: December 5, 2016
Phase: N/A
Study type: Interventional

An assessor blinded multi-centre randomized controlled trial will be conducted in which 60 participants will be randomized to either a novel task-specific approach to training bike skills or a parent-led home program comparison group. Baseline assessment will take place within 6 weeks prior to starting the intervention (T0) and outcomes will be assessed within a week following (T1); and at 12 - 14 weeks following (T2) the week long intervention. The primary outcome is attainment of individualised two-wheel bike specific goals at T1. All statistical analysis will be conducted on an intention-to-treat basis. Logistic regression will be used to assess the effect of providing the novel intervention compared to the parent-led home program on bike-specific goal attainment.

NCT ID: NCT03002285 Completed - Cerebral Palsy Clinical Trials

Fitts Law in People With Cerebral Palsy

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

Introduction: Cerebral palsy (CP) is a non-progressive disorder in the brain which makes the control and execution of movements difficult. One of the possible ways to analyze motor control in these individuals could be through analysis of movement speed and accuracy. Objective: To verify the speed-accuracy trade-off in individuals with CP. Method: 96 individuals were evaluated, 48 with CP and 48 with typical development (TD), matched by age and sex. The software used was the "Fitts' Reciprocal Aiming Task v.1.0 (Horizontal)", performed on a computer using an external optical mouse, with progressive indices of difficulty (IDs): ID2, ID4a and ID4b. Each index of difficulty was performed three times and the total time/touches captured.

NCT ID: NCT02998281 Completed - Cerebral Palsy Clinical Trials

Effects of Inspiratory Muscle Training in Children With Cerebral Palsy

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

Even if cerebral palsy not directly effect respiratory system, impairment of nervous and muscle systems, because of the brain damage, may cause respiratory functions impairment. In literature, it has been showed that children with cerebral palsy have decreased respiratory muscle strength and associated with trunk control, quality of life and respiratory functions. But, there is no study in literature that aims to increase respiratory muscle strength in these children. Hence, the aim of this study is to investigate effects of inspiratory muscle training on respiratory functions, trunk control, activities of daily living, functional exercise capacity and quality of life in children with cerebral palsy.

NCT ID: NCT02988557 Completed - Cerebral Palsy Clinical Trials

Walking Inclined Plane

Start date: February 21, 2017
Phase: N/A
Study type: Interventional

The adaptations in kinematics and muscle activity, investigated by 3D gait analysis and dynamic electromyography recordings, will be studied in children with bilateral spastic cerebral palsy during level walking, and before and after a training on a treadmill with a sloped surface (7°). Data will be compared with those obtained in a sample of typically developing (TD) children (controls)

NCT ID: NCT02984735 Completed - Cerebral Palsy Clinical Trials

Chewing Performance Level and Gross Motor Function in Children With Cerebral Palsy

Start date: January 2016
Phase:
Study type: Observational

The purpose of this study is to determine the association between gross motor function and chewing performance level in children with cerebral palsy (CP). A cross-sectional study was conducted in 152 children (ages 2-10y, 51.3% male) with a diagnosis of spastic CP. The Gross Motor Function Classification System (GMFCS) was used to determine gross motor function levels of children. Chewing performance level was determined by using the Karaduman Chewing Performance Scale (KCPS).

NCT ID: NCT02983708 Completed - Cerebral Palsy Clinical Trials

Neuroregenerative Potential of Intravenous G-CSF and Autologous Peripheral Blood Stem Cells

Start date: August 2011
Phase: Phase 1/Phase 2
Study type: Interventional

The current study describes a randomized, double-blind, cross-over study of intravenous G-CSF followed by infusion with autologous mobilized peripheral blood mononuclear cells (mPBMCs) in children with cerebral palsy (CP) to determine the safety and feasibility of the procedure, as well as the potential efficacy for improving neurological impairment.

NCT ID: NCT02979743 Recruiting - Cerebral Palsy Clinical Trials

MRI-based Neuroimaging Predictors of Clinical Improvements Following Therapy in Children With Cerebral Palsy

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

The aim of this study is to explore the relationship between brain MRI-metrics and hand function observed in children with cerebral palsy (CP),compared between baseline and the third month, and thus determine the early MRI-based neuroimaging predictor of clinical improvement following therapy in children with CP.

NCT ID: NCT02978469 Active, not recruiting - Cerebral Palsy (CP) Clinical Trials

Go For It: to Improve Levels of Daily Physical Activity and to Reduce the Sedentary Life Style of Adolescents With CP

Start date: May 2015
Phase: N/A
Study type: Interventional

Long hours of daily sitting and lack of Physical Activity (PA) are risk factors for morbidity and mortality. People with movement disabilities, including adolescents with Cerebral Palsy (CP) tend to lead a sedentary life styl and have have poor physical fitness. Adolescents with CP where found to be inactive most of the day thus, they are in greater risk of disease than the general population. In addition, over the years, people with disabilities experience physical and functional deterioration. Reducing sedentary behavior and increasing daily activity can reduce health risk factors among the adolescents with CP, reduce secondary impairments and preserve function. Interventions that included exercise alone has not resulted in physical activity and participating in a structured training did not continue after cessation intervention. The objectives of this study are to establish effective programs aiming to promote an active life style among adolescents and young adults with CP and to evaluate there outcomes. Specific objectives- Stage 1- Identifying barriers and facilitators for reducing sedentary behaviors and increasing physical activity among adolescents and young adults with CP. As well as, identifying mediators, needs and preferences for reducing sedentary behaviors and increasing physical activity among adolescents and young adults with CP. Stage 2- Based on stage 1- Establishing an intervention for reducing sedentary behaviors and increasing physical activity among adolescents. Stage 3- translating and developing questioners for the study. - Translating the ASK-Performance and the ASK-Capability questionnaires to Hebrew and validating the Hebrew translation. - Developing a self-efficacy perception questioner for increasing physical activity and reducing and sedentary behavior. - Translating to Hebrew, adjusting and validating an activity diary. Stage 4- evaluating the effectiveness of the proposed intervention program on reducing sedentary behaviors and increasing physical activity among adolescents and young adults with CP.

NCT ID: NCT02976532 Recruiting - Cerebral Palsy Clinical Trials

Controlling Femoral Derotation Osteotomy With Electromagnetic Tracking

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

The study is designed to evaluate the use of electromagnetic tracking in femoral derotation osteotomies. The goal is to raise the precision of the surgical procedure in order to improve the outcome in short- and long term. The electromagnetic tracking system is evaluated against a base line CT scan serving as reference standard.