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Metacognitive Therapy for Obsessive-Compulsive Disorder

Metacognitive Therapy for Obsessive-Compulsive Disorder

Recruiting
12-60 years
All
Phase N/A

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Overview

The goal of this clinical trial is to learn if metacognitive therapy can be effective in a Chinese sample of obsessive compulsive disorder (OCD) . The main questions it aims to answer

are

Can metacognitive therapy significantly reduce participants' levels of obsessive-compulsive symptoms? Can metacognitive therapy significantly improve participants' metacognitive adaptations?

The researchers will compare metacognitive therapy to a control condition without psychotherapy to see if metacognitive therapy is effective in treating OCD.

Participants will:

Receive the metacognitive therapy intervention or under control conditions for 8 to 15 weeks.

Be assessed for symptoms and metacognitive beliefs at pre-intervention, post-intervention and 12 weeks post-intervention

Description

This study will be a randomised controlled clinical trial. Participants who meet the enrolment criteria will be randomised into an experimental group and a control group. Participants in the experimental group will receive 8-15 weeks of metacognitive therapy, while participants in the control group will receive the same amount of time of regular treatment without psychotherapy components.

The researchers will assess participants' obsessive-compulsive symptoms and metacognitive levels before, after, and 12 weeks after the intervention. Assessment measures will be the Yale Brown Obsessive-Compulsive Scale (Y-BOCS) and the Metacognition Questionnaire (MCQ-30).

By comparing the assessment results of the two groups of participants, conclusions will be drawn as to whether metacognitive therapy can have a positive effect on a Chinese OCD sample.

Eligibility

Inclusion Criteria:

  • two psychiatrists with the title of Deputy Chief Physician or above jointly determine that the above diagnostic criteria were met
  • education level of junior high school or above, without mental retardation or audio-visual disorders
  • participation in the study is voluntary, and the informed consent is signed by the patient or his/her guardian

Exclusion Criteria:

  • loss of or insufficient self-awareness, the presence of hallucinations, delusions, and other psychotic symptoms
  • the presence of severe depression, or self-inflicted suicidal attempts and behaviors
  • the presence of a history of alcohol or drug abuse
  • refusal of psychotherapy, or the ineffectiveness of those who had been involved in a full course of psychotherapy.

Study details
    Obsessive-Compulsive Disorder

NCT06466057

Northeast Normal University

22 June 2024

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FAQs

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A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

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