Actively Recruiting

Age: 12Years +
All Genders
Healthy Volunteers
NCT06211517

Drugs Experience for Adolescents With Anorexia

Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-09-12

90

Participants Needed

1

Research Sites

184 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

The purpose of this study is to access to the experiences of adolescents, their parents and healthcare professionals regarding psychotropic drugs in anorexia nervosa. No preconceived ideas (according to qualitative methods) but a question: what are the participants' perceptions and experiences of psychotropic drugs in anorexia nervosa? In an adolescent medicine department.

CONDITIONS

Official Title

Drugs Experience for Adolescents With Anorexia

Who Can Participate

Age: 12Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 12 to 25 years
  • Diagnosed with restrictive or mixed anorexia nervosa according to DSM-5
  • Have received psychotropic drugs (antidepressants and/or atypical antipsychotics) during care, ongoing or discontinued
  • Parents of adolescents meeting the above criteria
  • Healthcare professionals working with adolescents with eating disorders
Not Eligible

You will not qualify if you...

  • Having an atypical eating disorder not meeting DSM-5 criteria for restrictive or mixed anorexia nervosa
  • Body mass index (BMI) less than 15
  • Prescribed an antidepressant other than an SSRI
  • Prescribed an atypical antipsychotic for psychotic symptoms

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Maison de Solenn Maison des Adolescents, Cochin Hospital

Paris, IDF, France, 75014

Actively Recruiting

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Research Team

M

Maude Ludot-Gregoire, MD, psychiatrist

CONTACT

M

Marie Benhammani-Godard

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

3

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