Genetic testing study for children with cerebral palsy
Part of Brain & nervous system, Mental health clinical trials.
This study looks for genetic reasons that may contribute to cerebral palsy. It may help families understand potential causes, especially when a specific genetic change is found.
Summary written for real people, not researchers, by Clin2.
Who can take part
- Your child is between 2 and 15 years old and has a diagnosis of cerebral palsy affecting one or both sides of the body
- Your child was born at 34 weeks of pregnancy or later
- You (the legal parent/guardian) agree to genetic testing for your child
- Both parents are available for genetic testing, if a particular kind of genetic change is found
- Your family is enrolled with the social security system
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
Similar studies
Other trials that look related to this one.
This study looks at how children with cerebral palsy walk compared to healthy children. Researchers use small sensors to measure movement, and the goal is to better understand walking problems.
This study is looking at how common different health problems are in children with cerebral palsy, and which problems often happen together. It may help clinicians plan better care by understanding the most frequent additional needs.
This study follows infants who already have cerebral palsy or who seem at high risk to develop it. It looks at early brain and movement signs over time, which may help doctors recognize CP sooner and plan support.
This trial uses a new, more detailed DNA test (long-read sequencing) to find the cause of severe epilepsy with developmental delays in children when standard genetic testing did not provide an answer. It aims to help families understand the genetic basis of their child's condition.
This study uses advanced genetic tests to find the cause of severe intellectual disability or related developmental disorders when standard tests found nothing. If you or your child qualify, the study may provide a clearer diagnosis and help guide care.
This study uses a special DNA test (trio exome sequencing) on a child or young adult and their two biological parents to look for a genetic cause of language and learning difficulties. If a genetic reason is found, it may help explain the cause and guide future care.
Hear when a new Cerebral Palsy trial opens
We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.