NCT07648108

Brief Summary

This study aims to evaluate the clinical, psychological, and functional outcomes of adolescents with anorexia nervosa receiving multidisciplinary care in hospital settings. Participants are treated either in a day hospitalization program or in a full-time inpatient program, in accordance with the French national guidelines (Haute Autorité de Santé, HAS) for the management of anorexia nervosa. The study seeks to better understand the evolution of patients' health status over time, including nutritional, psychological, and social dimensions, and to identify factors associated with treatment response. Data will be collected as part of routine clinical care without modification of the standard therapeutic management. The results of this study may help improve clinical practices and optimize care pathways for adolescents with anorexia nervosa.

Trial Health

65
Monitor

Trial Health Score

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

Enrollment
307

participants targeted

Target at P75+ for not_applicable

Timeline
8mo left

Started May 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

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

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress8%
May 2026Feb 2027

First Submitted

Initial submission to the registry

May 12, 2026

Completed
13 days until next milestone

Study Start

First participant enrolled

May 25, 2026

Completed
21 days until next milestone

First Posted

Study publicly available on registry

June 15, 2026

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 24, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 24, 2027

Last Updated

June 15, 2026

Status Verified

June 1, 2026

Enrollment Period

9 months

First QC Date

May 12, 2026

Last Update Submit

June 12, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Change in Body Mass Index (BMI)

    From admission request to at least 18 months follow-up

Secondary Outcomes (7)

  • Change in eating disorder psychopathology assessed by EDE-Q

    Baseline (at admission), discharge (end of hospitalization), and follow-up at least 18 months after admission

  • Change in body image concerns assessed by BSQ

    Baseline (at admission), discharge (end of hospitalization), and follow-up at least 18 months after admission

  • Change in anxiety and depression symptoms assessed by HADS

    Baseline (at admission), discharge (end of hospitalization), and follow-up at least 18 months after admission

  • Change in obsessive-compulsive symptoms assessed by MOCI

    Baseline (at admission), discharge (end of hospitalization), and follow-up at least 18 months after admission

  • Change in eating disorder-related quality of life assessed by EDQoL

    Baseline (at admission), discharge (end of hospitalization), and follow-up at least 18 months after admission

  • +2 more secondary outcomes

Study Arms (2)

Day Hospital Program

OTHER

Participants admitted to a specialized multidisciplinary day hospital program for eating disorders.

Other: Day Hospital Multidisciplinary Care

Non-Admitted Participants

OTHER

Participants who requested admission but were not admitted to the day hospital program.

Other: Standard Care Outside Day Hospital Program

Interventions

Participants admitted to the day hospital receive a multidisciplinary treatment program including psychiatric, medical, nutritional, and psychosocial care, delivered through structured daytime sessions without overnight stay.

Day Hospital Program

Participants not admitted to the day hospital program receive usual care according to standard clinical pathways outside the specialized day hospital setting.

Non-Admitted Participants

Eligibility Criteria

Age12 Years - 22 Years
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64)

You may qualify if:

  • Adolescents and young adults aged 12 to 22 years
  • Diagnosed with an eating disorder
  • Referred for admission to the day hospital program between October 2019 and December 2023
  • Provided informed consent (and parental consent for minors)

You may not qualify if:

  • Refusal to participate
  • Age below 12 years or above 22 years

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Feeding and Eating Disorders

Condition Hierarchy (Ancestors)

Signs and Symptoms, DigestiveSigns and SymptomsPathological Conditions, Signs and SymptomsMental Disorders

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Participants are assigned to groups based on admission status to a specialized day hospital program for eating disorders. This is a non-randomized quasi-experimental study comparing individuals admitted to the program and those not admitted, with outcomes assessed over time.
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

May 12, 2026

First Posted

June 15, 2026

Study Start

May 25, 2026

Primary Completion (Estimated)

February 24, 2027

Study Completion (Estimated)

February 24, 2027

Last Updated

June 15, 2026

Record last verified: 2026-06