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Cerebral Palsy clinical trials

View clinical trials related to Cerebral Palsy.

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NCT ID: NCT02003755 Completed - Cerebral Palsy (CP) Clinical Trials

The Effects of Continuous Passive Motion on Hypertonia of Soleus in Individuals With Cerebral Palsy

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

Cerebral palsy (CP) is a group of disorders of the development of movement and posture but often changing motor impairment syndromes. The spastic subtypes are the most common manifestations of cerebral palsy who perform movement difficultly due to hypertonia. Decease of spinal cord pathway, hyperactivity of alpha and gamma motoneuron and reduction of presynaptic inhibition may cause tendon reflex increase and hypertonia in individuals with CP. There are many ways to improve the hypertonia. In the past studies, the fast repeated range of motion could reduce muscle's activation effectively. The polyarticular movement training might increase joint range of motion and reduce the muscle activation. But the polyarticular movement training is difficulty for some individuals with CP. The single joint movement training may achieve the same effect as the polyarticular movement training. The purpose of this study was to investigate the effects of continuation passive range of motion (CPM) training whether could get the improvement of soleus hypertonia in individuals with CP.

NCT ID: NCT02002884 Completed - Cerebral Palsy Clinical Trials

Dose-response Study of Efficacy and Safety of Botulinum Toxin Type A to Treat Spasticity of the Arm(s) or of Arm(s) and Leg(s) in Cerebral Palsy

XARA
Start date: March 28, 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether injections of Botulinum toxin type A into muscles of one or both arms alone or in combination with injections into one or both legs are effective and safe in treating children/adolescents (age 2-17 years) with increased muscle tension/uncontrollable muscle stiffness (spasticity) due to cerebral palsy.

NCT ID: NCT01991145 Completed - Cerebral Palsy Clinical Trials

Allogeneic UCB Therapy With EPO in Children With CP

Start date: November 26, 2013
Phase: N/A
Study type: Interventional

This randomized controlled study aims to evaluate the efficacy and safety of allogeneic umbilical cord blood therapy combined with erythropoietin for children with cerebral palsy.

NCT ID: NCT01988844 Completed - Cerebral Palsy Clinical Trials

Upper Limbs Assessment in Children With Cerebral Palsy

Start date: November 2013
Phase: N/A
Study type: Observational

Cerebral palsy is the leading cause of physical disability among children. Manual dexterity and upper limbs functionality is limited between these children. The purpose of this study is to stablish a specific profile of school children with cerebral palsy based on the upper limbs assessment.

NCT ID: NCT01988584 Completed - Cerebral Palsy Clinical Trials

Safety and Effectiveness of Banked Cord Blood or Bone Marrow Stem Cells in Children With Cerebral Palsy (CP).

ACT for CP
Start date: November 2013
Phase: Phase 2
Study type: Interventional

The purpose of this study is to compare the safety and effectiveness of two types of stem cells,(either banked cord blood or bone marrow), in children between the ages of 2 to 10 years with CP. 15 children with banked cord blood at CBR and 15 children without banked cord blood will be enrolled into the study. The study involves one baseline/treatment visit and 3 follow-up visits at 6 months, 12 months, and 2 years. Five children in each group will be randomized to a placebo control group at the baseline/treatment visit. Parents will not be told if their child received stem cells or a placebo until the 12 month follow-up visit. At that time parents may elect to have their child receive the stem cell treatment; either bone marrow harvest or umbilical cord blood if banked with CBR. All study visits will be conducted at the UTHealth Medical School and Children's Memorial Hermann Hospital in Houston, Texas. As of 1/21/2014 we have met our enrollment limit for children without banked cord blood undergoing bone marrow harvest for stem cells.

NCT ID: NCT01973426 Completed - Clinical trials for Hemiplegic Cerebral Palsy

Evaluating Human-Machine Interfaces in a Robotic Thumb Orthosis

IOTA
Start date: October 2013
Phase:
Study type: Observational

We plan to investigate whether the Isolated Orthosis for Thumb Actuation (IOTA) can effectively facilitate the ability of participants to perform a specific set of clinically relevant tasks conducted in a clinic setting.

NCT ID: NCT01964664 Completed - Cerebral Palsy Clinical Trials

Mindfulness Meditation for Subjects With Severe Speech and Physical Impairments

MSPi
Start date: January 2013
Phase: N/A
Study type: Interventional

The purpose of this protocol is to (1) Determine whether a one-on-one mindfulness meditation intervention or audio training improves performance on an adaptive communication system that utilizes brain-computer interface (BCI); and (2) Determine whether the intervention reduces stress in subjects with severe speech and physical impairments (SSPI). Hypothesis: The group of subjects randomized to the mindfulness meditation training will improve BCI performance and stress levels more than the audio control group.

NCT ID: NCT01955655 Completed - Clinical trials for Recurrent Crying Spells

Recurrent Crying Spells in Cerebral Palsy

RCSCPSQ
Start date: December 2005
Phase: Phase 4
Study type: Interventional

This is a study of recurrent crying spells in Spastic Cerebral Palsy patients and their treatment.

NCT ID: NCT01952496 Completed - Cerebral Palsy Clinical Trials

Load Experienced While Using a Stander in Children With Cerebral Palsy

Start date: February 2014
Phase: N/A
Study type: Interventional

The goal of this project is to design and validate a force-measuring platform that will measure the magnitude and duration of the load experienced by the lower extremities of individuals with a neuromuscular disability who use a stationary assisted standing device to increase their Bone Mineral Density.

NCT ID: NCT01948154 Completed - Quality of Life Clinical Trials

The Relationship of Speech Function and Quality of Life in Children With Cerebral Palsy: A Longitudinal Study

Start date: February 2013
Phase: N/A
Study type: Observational [Patient Registry]

Cerebral palsy (CP) encompass a group of non-progressive, non-contagious motor conditions that cause physical disability in human development. It is not infrequently to note concurrent impairment in sensory, intelligence, vision and auditory in those patients. Many studies have documented Cerebral palsy is associated with a variety of neuromotor disorders that frequently affect the speech production system. The speech function impairment varied widely due to different severity of diseases involved. The investigators hypothesize such impairment of speech function may affect degree of social participation and eventually the quality of life (QoL).