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NCT06665802Completed

Avoidant and Restrictive Food Intake Disorders (ARFID) in Adolescence: Early Oral Development, Psychopathological Profile and Sensory Integration

Source: ClinicalTrials.gov · Last updated 6 May 2026

Brief summary (registry, in English)

The purpose of this study is to assess if adolescents affected with Avoidant and Restrictive Food Intake Disorders (ARFID) had more frequent precocious pediatric feeding disorders before 4 years old compared to healthy adolescents.

Status (registry)
Completed
Study type
Observational
Enrollment
60 (actual)
First submitted
24 Oct 2024
Start date
3 Feb 2025
Primary completion date
3 Feb 2025
Lead sponsor
Assistance Publique - Hôpitaux de Paris
Diseases
Autism
NCT number
NCT06665802

What you commit to

  • Study type: Observational
  • Participants enrolled: 60
  • From 3 Feb 2025 to the primary completion date, 3 Feb 2025
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • \- Diagnosis of autism spectrum disorder already made at the time of the consultation
  • \- Presence of a chronic organic or psychological illness, to limit the risk of including non ARFID patients at high risk of eating disorders

Other

  • For all patients:
  • \- Parents and adolescents who do not speak French well enough to understand the questions on the scales and questionnaires
  • For ARFID patients:
  • For non-ARFID patients:

Who the study is looking for

  • For all patients:
  • Adolescent aged 12 to 18 (minors = 17 years 11 months)
  • No opposition from parents and adolescent
    • For ARFID patients:
  • Consulting at MDA or Necker for an ARFID diagnosed using DSM V criteria
  • Whose first consultation for this disorder was less than 2 years ago
    • For non-ARFID patients:
  • Consulting or hospitalized in orthopaedic surgery at Necker Hospital or Robert Debré Hospital for an acute traumatic reason
  • Not diagnosed with a chronic illness

Age in the registry: 12 years to 17 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hopital Necker Enfants Malades
Coordinator of this site? Confirm its status
ParisFranceUnknown status
Hopital Robert Debre
Coordinator of this site? Confirm its status
ParisFranceUnknown status
Hôpital Cochin
Coordinator of this site? Confirm its status
ParisFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.