Actively Recruiting

Age: 3Years - 17Years
All Genders
NCT06737718

Use of Eye Tracking to Study Social Perception Abnormalities in Children With Angelman Syndrome

Led by Assistance Publique - Hôpitaux de Paris · Updated on 2026-03-16

60

Participants Needed

1

Research Sites

100 weeks

Total Duration

On this page

Sponsors

A

Assistance Publique - Hôpitaux de Paris

Lead Sponsor

U

URC-CIC Paris Descartes Necker Cochin

Collaborating Sponsor

AI-Summary

What this Trial Is About

Angelman syndrome (AS) is a rare neurogenetic disorder that affects approximately 1 in 15,000 children - approximately 500,000 people worldwide. It is a major neurodevelopmental disorder characterized by severe developmental delay with significant intellectual disability, lack of oral language, motor, balance, and sensory impairments. While basic research and clinical trials are progressing, the scientific community is still searching for key biomarkers to assess significant improvements in individuals participating in clinical trials. Eye tracking has been widely used in the diagnosis of social perception abnormalities in children with autism spectrum disorder, as has already been the case for other rare neurodevelopmental diseases. However, few studies have highlighted the usefulness of eye tracking as a diagnostic tool for social behavioral disorders in individuals with Angelman syndrome. Given the prevalence of autistic-like symptoms in patients with AS, if eye-tracking can identify abnormalities in social perception in children with Angelman syndrome, these measurements could become a biomarker for therapeutic studies in these patients.

CONDITIONS

Official Title

Use of Eye Tracking to Study Social Perception Abnormalities in Children With Angelman Syndrome

Who Can Participate

Age: 3Years - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Children diagnosed with Angelman syndrome by genetic testing or EEG
  • Healthy volunteer children with no known genetic or psychiatric neurological disorders for control group
  • Aged between 3 and 17 years
  • Male or female
  • Parent or legal guardian consents and child is informed and not opposed to participation
Not Eligible

You will not qualify if you...

  • Refusal to participate in the study

AI-Screening

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Trial Site Locations

Total: 1 location

1

Hôpital Necker-Enfants Malades

Paris, France, 75015

Actively Recruiting

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Research Team

N

Nathalie MD, PhD Boddaert

CONTACT

V

Victor Bruyere

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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