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CP clinical trials

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NCT ID: NCT05739396 Active, not recruiting - Balance Clinical Trials

Core Stabalization and Rebound Therapy and CP

Start date: February 1, 2023
Phase: N/A
Study type: Interventional

the study aims to compare the effect of core stabalization and rebound therapy on balance in children with hemiplegic cerebral palsy

NCT ID: NCT04961749 Recruiting - Clinical trials for Gait Disorders, Neurologic

Retention of Whole-body Training Effects on Ambulatory Function in Children With Cerebral Palsy

CP_WBVT
Start date: June 17, 2021
Phase: N/A
Study type: Interventional

This study will evaluate the retention effects of a four-week whole-body vibration training intervention in children with Cerebral Palsy. The primary outcomes for this study are gait function, including Timed Up and Go and the two-minute walk test. Secondary outcomes of this study include lower extremity gait function, coordination, and gait variability. For this study, a total of 10 children with Cerebral Palsy (CP) will be recruited with 5 being randomly placed into an experimental group and 5 being randomly placed into a control group. Each participant, regardless of group, will complete pre-, post-, and retention testing, with a four-week whole-body vibration training intervention between the pre- and post-testing. The four-week whole-body vibration training will include three visits per week, with the experimental group receiving a vibration stimulus while standing on a vibration platform. Vibration sessions will consist of three-minutes of vibration, followed by three minutes rest, completing this cycle three separate times. The control group will follow a similar pattern, but rather than experiencing vibration, they will hear a sound of the vibration platform through a speaker. Once the four-week training session is finished, participants will return after a three-month retention period to determine whether ambulation function was retained.

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.