RecruitingNot ApplicableNCT06431854

Evaluation of a New Treatment Program for Adolescents With Eating Disorders: MINERVA Program

The Efficacy, Efficiency, and Patient Experience of a New Intensive Treatment Program for Adolescents With High-complexity Eating Disorders: MINERVA


Sponsor

Fundació Sant Joan de Déu

Enrollment

120 participants

Start Date

Oct 23, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

The aim of this study is to investigate the efficacy, efficiency, and patient experience of a new intervention program on adolescents with high-complexity eating disorders (ED). A prospective group of adolescents with ED (N=60) will follow this treatment program including four different phases: 1) Inpatient treatment; 2) Family Treatment Apartment; 3) Home Treatment; 4) Recovery within the community. The investigators will use a retrospective, control group (N=60) that matched the prospective group in age, sex, ED diagnosis, and severe symptomatology. Primary variables regarding Body Mass Index (BMI), ED symptomatology, functionality, recovery (yes/no), type of outpatient services (low/mid/high intensity), number of readmissions, and patient experience will be assessed at discharge, and after 6 and 12 months. Secondary variables include anxiety, depression, readiness to recover, quality of life symptoms, caregiver skills, and functionality of the family


Eligibility

Min Age: 12 YearsMax Age: 17 Years

Inclusion Criteria12

  • Patient diagnosed with an Eating Disorder (according to the DSM-5) through a semi-structured interview (K-SADS PL-5)
  • Aged between 12 and 17 years old
  • Both patients and parents are willing to participate in the study and sign the informed consent to accept participation
  • Patient with a poor response to treatment, defined as having one of the following two conditions:
  • undergoing over a year of treatment, including partial and total hospitalization, without symptom stabilization, experiencing severe psychological distress, eating symptomatology, comorbidities, or family dysfunction during this period (clinical improvement of at least 50 on the CGAS functioning scale) OR
  • undergoing more than three admissions without symptom stabilization (clinical improvement of at least 50 on the CGAS functioning scale).
  • Aged between 12 and 17 years old
  • Diagnosed with an Eating Disorder (according to the DSM-5)
  • Received treatment in Sant Joan de Déu between 2012 and 2022
  • Patient with a poor response to treatment, defined as having one of the following two conditions:
  • undergoing over a year of treatment, including partial or total hospitalization, without achieving stabilization of ED symptomatology (needing high-intensive treatment units i.e. not being able to follow individual treatment in external consultations) OR
  • undergoing more than three admissions without symptom stabilization once referred to partial hospitalization in less than one year, including a similar psychological state and characteristics as the first condition

Exclusion Criteria2

  • Acute ED pathology and biological decompensation that require urgent pediatric attention or admission to an acute psychiatric ward.
  • Missingness of 20% or more of the required data

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

BEHAVIORALED-MINERVA Program

ED-MINERVA Program aims to improve ED symptoms and related difficulties of the patient and provide tools to enhance the family's management (nutritionally, emotionally, and behaviorally) in their natural environment. The treatment consists of four phases with a gradually decreasing therapeutic intensity, ranging from total hospitalization, family treatment apartment, to home treatment and subsequent linkage with specialized local facilities. The ED-MINERVA program uses various aspects of family-based treatment, cognitive behavioral therapy, dialectical behavioral therapy, and systemic family therapy.


Locations(1)

Hospital Sant Joan de Déu

Barcelona, Spain

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06431854


Related Trials