Plain-English translation of NCT06877715 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
This study is looking at how autism-related traits and sensory sensitivities show up in children with Prader-Willi Syndrome. Researchers want to understand whether children with this genetic condition experience autism differently than other children, and how past oxytocin treatment might affect these traits. By learning more, doctors hope to better recognize and help children with Prader-Willi Syndrome who also have autism-like characteristics.
Right now, doctors in France rarely check for autism in children with Prader-Willi Syndrome, even though many of these children show autism-related behaviors. This study exists to fill that gap and help doctors understand exactly what autism looks like in this specific genetic condition, so children can get the right support earlier.
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Your child would complete special assessments and questionnaires during visits that are already planned as part of their regular Prader-Willi Syndrome care at the hospital. These assessments will look at autism-related behaviors and how your child responds to sensory experiences like sounds, textures, and lights. The study team will also review your child's medical records, including whether they received oxytocin treatment when younger.
AI-generated summary from trial data · Jun 2, 2026 · Not medical advice
France