Actively Recruiting

Phase Not Applicable
Age: 13Years - 19Years
All Genders
NCT07435818

Feasibility and Acceptability of Metacognitive Training for Eating Disorders in Adolescents With Anorexia Nervosa

Led by University of Évora · Updated on 2026-03-13

14

Participants Needed

1

Research Sites

65 weeks

Total Duration

On this page

Sponsors

U

University of Évora

Lead Sponsor

F

Fundação para a Ciência e a Tecnologia

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study aims to assess the feasibility and acceptability of Metacognitive Training for Eating Disorders (MCT-ED) in adolescents with anorexia nervosa and atypical anorexia nervosa.

CONDITIONS

Official Title

Feasibility and Acceptability of Metacognitive Training for Eating Disorders in Adolescents With Anorexia Nervosa

Who Can Participate

Age: 13Years - 19Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adolescents aged 13 to 19 years
  • Diagnosis of Anorexia Nervosa or Atypical Anorexia Nervosa confirmed by a child and adolescent psychiatrist using DSM-5-TR or ICD-11
  • Currently followed in an Eating Disorder Outpatient Consultation
  • Fluent in Portuguese
Not Eligible

You will not qualify if you...

  • Acute suicidal ideation or behavior requiring immediate clinical intervention
  • Imminent risk of hospitalization due to clinical deterioration
  • Current diagnosis of psychotic disorder, bipolar disorder, or substance dependence
  • Any clinical condition deemed by the treating clinician to make videoconference-based participation inappropriate

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

Hospital Beatriz Ângelo - Unidade Local de Saúde Loures-Odivelas, Child and Adolescent Psychiatry Service, Department of Psychiatry and Mental Health, Loures, Portugal

Loures, Portugal

Actively Recruiting

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Research Team

A

Andreia Espírito Santo, PhD Student

CONTACT

L

Lara Pinho, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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