Examining autistic traits and sensory profiles in children with Prader-Willi Syndrome

Autistic Symptomatology and Sensory Profile in Children With Prader-Willi Syndrome

Observational University Hospital, Toulouse · NCT06877715

This study looks at how autistic traits and sensory experiences show up in children with Prader-Willi Syndrome to better understand their needs and see if early oxytocin treatment makes a difference.

Quick facts

Study typeObservational
Enrollment75 (estimated)
Ages3 Years to 16 Years
SexAll
SponsorUniversity Hospital, Toulouse Academic / other
Locations1 site (Toulouse)
Trial IDNCT06877715 on ClinicalTrials.gov

What this trial studies

This observational study focuses on children diagnosed with Prader-Willi Syndrome (PWS) to explore their autistic symptomatology and sensory profiles. It aims to identify the unique characteristics of autism in PWS, which is often overlooked in standard care. The study will involve psychological and sensory assessments, and it will also consider the effects of early oxytocin treatment on these traits. By aligning with recommendations for early intervention, the study seeks to improve understanding and management of PWS-related challenges.

Who should consider this trial

Good fit: Ideal candidates for this study are children aged 3 to 16 years with genetically confirmed Prader-Willi Syndrome.

Not a fit: Patients who have recently changed their psychotropic treatment or are unable to provide clear information may not benefit from this study.

Why it matters

Potential benefit: If successful, this study could lead to better identification and tailored interventions for children with Prader-Willi Syndrome and associated autistic traits.

How similar studies have performed: While there is limited research specifically on PWS and autism, studies on similar neurodevelopmental disorders have shown the importance of early intervention and tailored assessments.

Eligibility criteria

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Child with genetically confirmed PWS and identification of genetic subtype;
* Child aged between 3 and 16 years;
* Hospitalisation or multidisciplinary consultation planned for the child's routine follow-up at one of the investigating centres;
* No parental/legal guardian objection.

Exclusion Criteria:

* Change in psychotropic treatment (start, change in dose or discontinuation) in the past 3 months;
* Inability to provide clear information to parents/legal guardian;
* Not covered by social security.

Where this trial is running

Toulouse

Study contacts

How to participate

  1. Review the eligibility criteria above with your treating physician.
  2. Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
  3. Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions Prader-Willi SyndromePrader-Willi syndromeAutism Spectrum DisorderAutistic SymptomatologySensory profile
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.