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Recruiting NCT06800911

Metacognitive Beliefs in Obese Patients

— Observational Obesity

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: Questionnaires.
Who it may be relevant to
Registry conditions: Obesity. Basic parameters: 18 years — 65 years · All.
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 →

Unsure about the terms? Read our patient guide →

Official title

Metacognitive Beliefs, Emotional Regulation in Obese Patients

Overview

The study aims to investigate the presence of metacognitive beliefs, emotional regulation, and emotional eating in obese patients and their possible relationships.

Interventions

  • Other Questionnaires
    Metacognition Questionnaire Penn State Worry Questionnaire Ruminative Response Scale Anger Rumination scale Difficulties in Emotion Regulation Scale Emotional Eating subscale of the Dutch Eating Behavior Questionnaire

Primary outcome measures

  • Metacognitive beliefs [Time frame: Baseline]
  • Rumination [Time frame: Baseline]
  • Anger Rumination [Time frame: Baseline]
  • Emotional dysregulation [Time frame: Baseline]
  • Emotional eating [Time frame: Baseline]

Eligibility criteria

Inclusion criteria

  • Age: between 18 and 65 years
  • Italian nationality
  • Body Mass Index ≥ 35 kg/m2

Exclusion criteria

  • Psychiatric pathologies
  • Severe cognitive deficits that could compromise the completion of the questionnaires
  • Absence of signed informed consent

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

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

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

Identifiers

NCT: NCT06800911 · 01C415

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗