NCT06211517

Brief Summary

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.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
90

participants targeted

Target at P50-P75 for all trials

Timeline
19mo left

Started May 2024

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress56%
May 2024Dec 2027

First Submitted

Initial submission to the registry

January 8, 2024

Completed
10 days until next milestone

First Posted

Study publicly available on registry

January 18, 2024

Completed
4 months until next milestone

Study Start

First participant enrolled

May 20, 2024

Completed
2.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2027

Expected
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2027

Last Updated

September 12, 2025

Status Verified

September 1, 2025

Enrollment Period

2.9 years

First QC Date

January 8, 2024

Last Update Submit

September 5, 2025

Conditions

Anorexia NervosaPsychotropic DrugsAdolescent

Keywords

AdolescentsAnorexia nervosaPsychotropic drugsQualitative researchThematic analysis

Outcome Measures

Primary Outcomes (1)

  • Semi-structured interview

    Themes describing adolescent experiences regarding psychotropic drugs in anorexia nervosa - Emergence of themes describing participants' experience from analysis of qualitative interviews (with Interpretative Phenomenology Analysis methodology)

    Day of inclusion

Secondary Outcomes (2)

  • Semi-structured interview

    Day of inclusion

  • Semi-structured interview

    Day of inclusion

Study Arms (3)

Adolescents

Adolescents suffering from anorexia nervosa 12 to 25 years

Other: Semi-structured interviews with visual mediations

Parents

Parents whose adolescents suffer from anorexia nervosa

Other: Semi-structured interviews with visual mediations

Healthcare professionals

Healthcare professionals in charge of adolescents suffering from anorexia nervosa

Other: Semi-structured interviews

Interventions

Semi-structured interviews with visual mediationsOTHER

Semi-structured interviews with visual mediations / An hour-long interview

Also known as: Qualitative interviews
AdolescentsParents
Semi-structured interviewsOTHER

Semi-structured interviews

Also known as: Qualitative interviews
Healthcare professionals

Eligibility Criteria

Age12 Years+
Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adolescent medicine department in Cochin hospital

You may qualify if:

  • Adolescents :
  • Aged 12 to 25 years
  • Suffering from anorexia nervosa (restrictive or mixed) according to DSM-5 (Diagnostic and Statistical Manual) criteria
  • Received psychotropic drugs (antidepressant treatment and/or APA) during their care, either ongoing or discontinued before this study started
  • Healthcare Professionals working with adolescents suffering from eating disorders

You may not qualify if:

  • Adolescents :
  • Atypical eating disorder that does not meet the DSM-5 criteria for restrictive or mixed anorexia nervosa
  • BMI\<15
  • Prescription of an antidepressant other than an SSRI (Selective Serotonin Reuptake Inhibitor)
  • Prescription of an APA for the indication of psychotic symptoms

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Maison de Solenn Maison des Adolescents, Cochin Hospital

Paris, IDF, 75014, France

RECRUITING

Related Publications (1)

  • Ludot-Gregoire M, David V, Carretier E, Lachal J, Moro MR, Blanchet C. Subjective Experience of Antidepressant Prescription Among Adolescents With Anorexia Nervosa. Front Psychiatry. 2022 Apr 4;13:770903. doi: 10.3389/fpsyt.2022.770903. eCollection 2022.

    PMID: 35444576BACKGROUND

Related Links

MeSH Terms

Conditions

Anorexia Nervosa

Condition Hierarchy (Ancestors)

Feeding and Eating DisordersMental Disorders

Study Officials

  • Corinne Blanchet, MD

    Cochin Hospital (maison de Solenn)

    STUDY DIRECTOR

  • Marie Rose Moro, MD, PhD

    Cochin Hospital (maison de Solenn)

    STUDY DIRECTOR

  • Maude Ludot-Gregoire, MD

    Cochin Hospital (maison de Solenn)

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Maude Ludot-Gregoire, MD, psychiatrist

CONTACT

00 33 1 58 41 28 41maude.ludot@aphp.fr

Marie Benhammani-Godard

CONTACT

00 33 1 58 41 11 90marie.godard@aphp.fr

Study Design

Study Type
observational
Observational Model
OTHER
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 8, 2024

First Posted

January 18, 2024

Study Start

May 20, 2024

Primary Completion (Estimated)

May 1, 2027

Study Completion (Estimated)

December 1, 2027

Last Updated

September 12, 2025

Record last verified: 2025-09

Data Sharing

IPD Sharing
Will not share

Locations

FR(1)