Plain-English translation of NCT06149468 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This is a research project that gathers medical and personal information from children and adolescents with autism who visit or are followed at autism specialist centers in French-speaking Belgium. By collecting detailed information from many young people with autism, researchers hope to better understand the condition, learn about different types of autism, and improve how doctors care for children with autism.
Many questions about autism remain unanswered—including questions about genetics, how the brain works in autism, and language development. By gathering careful information from a large group of children and teens with autism, researchers can conduct rigorous studies to advance understanding and develop better treatments and support.
You likely qualify if…
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If your child is already visiting an autism reference center in Belgium, participation involves allowing the center to share your child's medical and personal information with the research database. The researchers will collect general information about your family, your child's autism diagnosis, and track how your child develops over time. You would not need to do anything extra beyond your regular visits to the autism center.
AI-generated summary from trial data · Jun 8, 2026 · Not medical advice
Belgium
Collaborators
Université Libre de Bruxelles, Université de Namur
Enrollment target
~500 participants
Started
September 2023
Primary completion
December 2028
Last updated on clinicaltrials.gov in May 2025.
Reach out to the team running this trial. Response times vary — some teams are faster than others.
Central contact
Marie-Cécile Nassogne, Prof
Université Catholique de Louvain
Tell us you're interested and we'll help connect you with the research team. We'll walk you through what to expect first — no email needed to get started.