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Cerebral Palsy clinical trials

View clinical trials related to Cerebral Palsy.

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NCT ID: NCT03518541 Recruiting - Cerebral Palsy Clinical Trials

Controlling Femoral Derotation Osteotomy In Cerebral Palsy With Electromagnetic Tracking

Start date: December 1, 2017
Phase: N/A
Study type: Interventional

The study is designed to evaluate the use of electromagnetic tracking in transversal plane 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. All patients are examined with an instrumented 3D gait analysis pre- and one year postoperatively. The electromagnetic tracking system is evaluated against a base line CT or MRI scan serving as reference standard pre- and postoperatively.

NCT ID: NCT03508583 Not yet recruiting - Cerebral Palsy Clinical Trials

Turkish Version of The Measure of Processes of Care (MPOC)

Start date: May 1, 2018
Phase:
Study type: Observational

Family-centred care (FCS) is considered the best practice in providing rehabilitation to children with disabilities and special needs. Family-centred care has been described as a partnership approach to healthcare decision making. As a philosophy of healthcare, today many multidisciplinary healthcare facilities have organized their services according to a family-centred approach. TheMeasure of Processes of Care (MPOC) is the most widely used instrument to assess parents' self-reported experiences of family-centred behaviours of rehabilitation services providers. The aim of this study is to translate the scale to Turkish and to determine validity and reliability of The Measure of Processes of Care (MPOC 56- 20- SP)

NCT ID: NCT03506841 Completed - Cerebral Palsy Clinical Trials

Cerebrolysin and Neurodevelopment in Preterm Infants

Start date: June 2016
Phase: Phase 1
Study type: Interventional

The overall aim of the study is to assess the effect of Cerebrolysin on physical and mental development of preterm infants by Denver Scale II at different ages of 5, 7 and 12 months

NCT ID: NCT03504787 Completed - Cerebral Palsy Clinical Trials

Upper Extremity Selective Voluntary Motor Control in Children With Unilateral Cerebral Palsy

Start date: April 25, 2017
Phase:
Study type: Observational

The aim of the study was to determine upper extremity selective motor control (SMC) in Children with Unilateral Cerebral Palsy (CP). It was also aimed to determine the relationship between upper extremity SMC and upper extremity functions in unilateral CP.

NCT ID: NCT03499288 Completed - Cerebral Palsy Clinical Trials

Profiling Children and Youth With Cerebral Palsy in Relation to Feeding and Nutrition

Purple-N
Start date: April 11, 2017
Phase:
Study type: Observational

HCPs will complete questionnaires about their patients with Cerebral Palsy (CP) and invite parents/caregivers of these patients to fill in questionnaires as well. Questionnaires include questions on individualized treatment, nutritional profile and management, and patient characteristics.

NCT ID: NCT03490591 Completed - Cerebral Palsy Clinical Trials

Robot-assisted Hand Rehabilitation for Children With Cerebral Palsy: a Pilot Study

Start date: April 15, 2018
Phase: N/A
Study type: Interventional

Objective: To investigate the effects of robot-assisted hand rehabilitation with a Gloreha device on hand function and the participation of ADL for children with cerebral palsy(CP). Materials and Methods: Five children with CP aged 6 to 18 years were recruited and received 12times of robot-assisted hand rehabilitation for 6 weeks of treatment (Sixty minutes a time, twice a week). The performance was assessed by a assessor for three times (pre-test, post-test, follow up at one month). The outcome measures Fugl-Meyer Assessment-Upper Limb section(FMA-UE),Box and block test(BBT), Maximal voluntary contraction(MVC) of extensor digitorum communis(EDC), Flexor digitorum(FD), Grasp strength, & ABILHAND-Kids for ADL ability. Collected data will be analyzed with ANOVA test by SPSS version 20.0, and alpha level was set at .05. Our hypothesis are robot-assisted hand rehabilitation with a Gloreha device has positive effects on hand function and the participation of ADL for children with CP.

NCT ID: NCT03486483 Completed - Clinical trials for Spastic Cerebral Palsy

Spastic Cerebral Palsy and Slackline

SCPSLACK
Start date: April 1, 2015
Phase: N/A
Study type: Interventional

The aim of the present study was to assess whether supervised slackline training improves postural control in children and teenagers with spastic cerebral palsy (grade I and II of the Gross Motor Function Classification System).

NCT ID: NCT03484078 Active, not recruiting - Clinical trials for Cerebral Palsy, Spastic

Effect of Vibration on Muscle Properties, Physical Activity and Balance in Children With Cerebral Palsy

Start date: January 23, 2019
Phase: N/A
Study type: Interventional

The aim of the 6-month randomized controlled trial, with 6-month no treatment follow-up, is to examine the effects of low-magnitude vibration on muscle, physical activity, and balance in children with spastic cerebral palsy.

NCT ID: NCT03474848 Completed - Cerebral Palsy Clinical Trials

The Effects of Hand-Arm Bimanual Intensive Training (HABIT) in Children With Bilateral Cerebral Palsy

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

Hand-Arm Bimanual Intensive Training (HABIT) has been shown to result in improvements in hand function and daily functioning of children with unilateral cerebral palsy (CP). Children with bilateral CP may also present difficulties to coordinate their hands to perform activities. Thus, HABIT may be a potential intervention for these individuals. We intend to examine the effects of HABIT on hand function and daily functioning of children with bilateral CP compared with conventional occupational therapy (OT). Our hypothesis is that children receiving HABIT will present larger improvements in manual dexterity and daily functioning as compared to conventional OT.

NCT ID: NCT03473301 Completed - Cerebral Palsy Clinical Trials

A Study of UCB and MSCs in Children With CP: ACCeNT-CP

ACCeNT-CP
Start date: April 10, 2018
Phase: Phase 1/Phase 2
Study type: Interventional

The main purpose of this study is to estimate change in motor function 12 months after treatment with a single dose of allogeneic umbilical cord blood (AlloCB) or repeated doses of umbilical cord tissue-derived mesenchymal stromal cells (hCT-MSC) in children with cerebral palsy. In addition, this study will contribute much needed data to the clinical trials community on the natural history of the motor function in CP over short-term (less than 1 year) time periods relevant to the conduct of clinical trials and assess the safety of AlloCB and hCT-MSC infusion in children with cerebral palsy.