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Recruiting NCT06800807

Metacognitive Beliefs in Adolescents With Eating and Nutrition Disorders

Observational Feeding and Eating Disorders

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Observation of several factors involved in eating and nutrition disorders.
Who it may be relevant to
Registry conditions: Feeding and Eating Disorders. Basic parameters: 12 years — 17 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Italy
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Metacognitive Beliefs and Eating and Nutrition Disorders in Adolescents With Eating and Nutrition Disorders

Overview

The present study aims to study the presence of metacognitive beliefs in adolescent subjects with eating and nutrition disorders (END) compared with a control group composed of subjects of the same sex and age belonging to the general population.

Interventions

  • Other Observation of several factors involved in eating and nutrition disorders
    Observation of symptomatology of eating and nutrition disorders, metacognitive beliefs, brooding and rumination.

Primary outcome measures

  • Metacognitive beliefs [Time frame: Baseline]
  • Brooding [Time frame: Baseline]
  • Rumination [Time frame: Baseline]

Eligibility criteria

Eating and nutrition disorders (END)

Inclusion criteria

  • Female sex
  • Age: 12 to 17 years
  • Italian nationality
  • Diagnosis relating to the END framework according to the diagnostic criteria of the Diagnostic and Statistical Manual of Mental Disorders (DSM-5).

Exclusion criteria

  • Absence of signed Informed Consent

Control group

Inclusion criteria

  • Female sex
  • Age: 12 to 17 years
  • Italian nationality

Exclusion criteria

  • Absence of signed Informed Consent

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Study design

Observational model
Cohort

Study locations

Italy · 1 center
  • Istituto Auxologico Italiano IRCCS, Site Piancavallo — Oggebbio

Identifiers

NCT: NCT06800807 · 01C412

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗