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Cerebral Palsy clinical trials

View clinical trials related to Cerebral Palsy.

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NCT ID: NCT01158833 Completed - Cerebral Palsy Clinical Trials

Validity of the Kinematic Classification of Gait in Diplegic Children With Cerebral Palsy (CP)

Start date: April 2010
Phase: N/A
Study type: Observational

In recent years Ferrari et al. proposed a new classification of gait in diplegic children with spastic diplegia that describes four different patterns of gait by analyzing the strategies that each children adopts to need his/her needs to walk. The investigators believe that this classification provides the clinician with clinically meaningful information in terms of coping strategies adopted to maximize the ability to walk. The aim of this study is to determine the criterion validity of the new classification of the pattern of gait in children with spastic diplegia by correlating pattern of diplegic gait with the score of the Functional performance measure.

NCT ID: NCT01157494 Completed - Cerebral Palsy Clinical Trials

Validity of Manipulation Taxonomy of Spastic Hemiplegic Cerebral Palsy (CP) Forms

Start date: April 2010
Phase: N/A
Study type: Observational

In recent years Ferrari et al. proposed a new classification of manipulation in children with spastic hemiplegia which describes five different classes by analyzing and integrating the kinematic patterns of the hand and its functional use. The investigators believe that this classification provides the clinician with clinically meaningful information, by identifying the useful strategies spontaneously adopted by the children during manipulation tasks. The aim of this study is to determine the criterion validity of the new classification of the pattern of manipulation in children with spastic hemiplegia by correlating hand manipulation classes with both the scores of the Assisting Hand Assessment and the scores of the Melbourne Assessment of Unilateral Upper Limb Function.

NCT ID: NCT01147653 Completed - Cerebral Palsy Clinical Trials

A Randomized Study of Autologous Umbilical Cord Blood Reinfusion in Children With Cerebral Palsy

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

The purpose of this study is to determine the efficacy of a single intravenous infusion of autologous umbilical cord blood (UCB) for the treatment of pediatric patients with spastic cerebral palsy.

NCT ID: NCT01117090 Completed - Multiple Sclerosis Clinical Trials

Measuring Signatures in the Fluid Surrounding the Spinal Cord in Patients Who Have Problems With Intrathecal Drug Delivery

Start date: June 2010
Phase: N/A
Study type: Observational

The purpose of this study is to record signatures from the fluid surrounding the spinal cord from people who have an implanted drug infusion system.

NCT ID: NCT01115998 Completed - Cerebral Palsy Clinical Trials

Effect of Power Wheelchairs on the Development and Function of Young Children With Severe Physical Disabilities

Start date: June 2002
Phase: Phase 2
Study type: Interventional

Self-produced locomotion often is limited in children with cerebral palsy and other conditions that cause severe motor impairments. As a result, these children may be at risk for secondary impairments in spatial cognition, communication, social development, and other domains influenced by independent mobility. To compensate, power mobility has increasingly been advocated for young children with severe motor impairments. The study hypotheses were: 1. Children with severe disabilities that prevent independent locomotion who learn to use power mobility devices when they are 14- to 30-months-of-age will have greater communication, social, and cognitive development over a 12-month period, and will demonstrate more competent coping skills than children with the same characteristics who do not use power mobility. 2. Parents of children who use power mobility will view it as a positive influence on their children's lives, and will perceive their children's development to be more mature than the parents of children who do not use power mobility will perceive their children's development.

NCT ID: NCT01092637 Completed - Cerebral Palsy Clinical Trials

The TOBY Children Study

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

The aim of this study is to determine the efficacy of therapeutic hypothermia following perinatal asphyxia on neurological and neuropsychological outcomes and also to assess academic attainment and any additional health, societal or educational costs associated with changes in outcome as a result of the intervention. This study will determine whether the apparent initial benefits of cooling are maintained in the longer term. Perinatal asphyxia (a lack of oxygen occurring around the time of birth) may have long term consequences on brain functioning, which may be altered by treatment with hypothermia (cooling). Currently, there is no information on the effect of cooling on outcome beyond 18 months of age. We intend to assess at 6 - 7 years of age, the children that participated in the TOBY trial of whole body cooling following perinatal asphyxia and compare between the children that had received the cooling treatment soon after birth and those that were not treated with cooling, the number that survived with an intelligence quotient (IQ) greater than 84, the presence and severity of disabilities, educational attainment and the economic impact on families and service providers. If possible, children will be assessed in their school, with the option of alternative venues such as home or clinic if required. During the assessment a paediatrician will conduct a neurological examination. A psychologist will administer psychometric tests to evaluate cognitive, behavioural and motor development. Questionnaires completed by parents and teachers will complete the data collection. Economic factors will also be assessed in the parent questionnaire. Each child will have contact with the assessors during one school day with appropriate breaks. Assessments will take place over a period of 3 years.

NCT ID: NCT01086670 Completed - Cerebral Palsy Clinical Trials

Physical, Functional and Neural Effects of Two Lower Extremity Exercise Protocols in Children With Cerebral Palsy

Start date: March 30, 2010
Phase: Phase 1/Phase 2
Study type: Interventional

Background: - Many people who have cerebral palsy (CP) have spastic diplegia, which affects the legs and causes difficulty with leg movement and walking. Research has shown that exercise can help those with CP learn to move their arms better, but more research is needed to determine whether exercise programs can improve leg movements in people with CP. - Walking on a treadmill with the help of a physical therapist has improved the treatment outcomes of some individuals with spinal cord injuries. Many children with CP already have physical therapy but still have trouble with walking and leg coordination. Two other kinds of exercise machines, a stationary bicycle and an elliptical machine, used in the home, may be able to help children with CP walk better and move their legs better. Objectives: - To see how children with cerebral palsy (CP) move their legs differently from children without CP. - To see if an exercise program can improve leg coordination in children with CP. Eligibility: - Children between 5 and 17 years of age who either have spastic diplegia CP or are healthy volunteers. Design: - Children who are able and willing will have magnetic resonance imaging (MRI) scans at the start and the end of the study. - During Part I of the study, participants will demonstrate their leg and muscle function with the following tests: - Measurement of leg size and movement - Combined camera motion study and electrical impulse evaluation to assess how well the participant walks (with or without an assistive device, as needed) - Leg movement tests on an exercise bicycle and elliptical machine - Tests of leg muscle strength, stiffness, and effectiveness - Ultrasound scans of leg muscle - Parents of participants will complete computer-based questionnaires about their child s motor abilities. - A smaller group of participants will continue to Part II of the study, which involves regular exercise of 20 minutes a day, 5 days a week, for 3 months, on a stationary bicycle or elliptical trainer. Half of the group will start this exercise program immediately after the first part of the study, while the other half will wait 3 months before beginning the exercise program. - During Part II, participants will return to the clinical center for two more sets of the tests and evaluations performed in Part I.

NCT ID: NCT01078766 Enrolling by invitation - Cerebral Palsy Clinical Trials

Constraint-induced Movement Therapy and Hand Arm Bimanual Training in Children With Hemiplegic Cerebral Palsy (CP)

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

The combination of the constraint-induced movement therapy (CIMT) method as a complement to hand arm bimanual training (HABIT) will improve the frequency and quality of cooperative hand use and function in children with hemiplegic CP.

NCT ID: NCT01076257 Completed - Cerebral Palsy Clinical Trials

Efficacy of Modified Constraint-induced Movement Therapy in Children With Brain Damage

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

This research centers on the comparison of the immediate efficacy (right after therapy) and the maintained efficacy (3 months and 6 months) between "Modified Constraint-Induced Movement Therapy" (mCIMT) group and control group at different age.

NCT ID: NCT01072370 Withdrawn - Cerebral Palsy Clinical Trials

Safety and Effectiveness of Cord Blood Stem Cell Infusion for the Treatment of Cerebral Palsy in Children

Start date: January 2010
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to test the safety and effectiveness of a cord blood infusion in children who have motor disability due to cerebral palsy (CP). The subjects will be children whose parents have saved their infant's cord blood, who have non-progressive motor disability, and whose parents intend to have a cord blood infusion.