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An OCD Prevention Programme for at Risk Adults

An OCD Prevention Programme for at Risk Adults

Recruiting
18-65 years
All
Phase N/A
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Overview

The main purpose of this randomised clinical trial is to test the efficacy of a prevention program for adult who are at risk of developing OCD, thus constituting a form of tertiary prevention.

Description

After being informed about the study and giving written informed consent, all eligible participants will be randomised into the experimental group or the control group (TAU). Participants will be blind to the group allocation.

The experimental group will undergo a two weeks OCD prevention program, consisting of three group sessions per week.

The control group will not receive any intervention.

Researchers will compare the experimental group to the control group to test wether the prevention programme is efficient in reducing OCD symptomatology.

Eligibility

Inclusion Criteria:

  • age over 18

Exclusion Criteria:

  • clinically diagnosed OCD
  • current psychiatric/psychotherapeutic treatment
  • personality disorder diagnosis
  • suicidal ideation

Study details
    Obsessive-Compulsive Disorder

NCT06262464

Babes-Bolyai University

22 March 2024

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FAQs

Learn more about clinical trials

What is a clinical trial?

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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Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

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