Evaluation of a Day Hospital Program for Adolescents and Young Adults With Eating Disorders
UDJ-TCA
Evaluation of the Contribution of a Specialized Day Hospital for Adolescents and Young Adults With Eating Disorders: Long-Term Clinical Outcomes and Cross-Reported Experiences
1 other identifier
interventional
307
0 countries
N/A
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started May 2026
Shorter than P25 for not_applicable
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
First Submitted
Initial submission to the registry
May 12, 2026
CompletedStudy Start
First participant enrolled
May 25, 2026
CompletedFirst Posted
Study publicly available on registry
June 15, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 24, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
February 24, 2027
June 15, 2026
June 1, 2026
9 months
May 12, 2026
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
OTHERParticipants admitted to a specialized multidisciplinary day hospital program for eating disorders.
Non-Admitted Participants
OTHERParticipants who requested admission but were not admitted to the 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.
Participants not admitted to the day hospital program receive usual care according to standard clinical pathways outside the specialized day hospital setting.
Eligibility Criteria
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
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- 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