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An OCD Prevention Programme for at Risk Adults — ØCD  

Obsessive-Compulsive Disorder Clinical Trial

Official title:
The Efficacy of an OCD Prevention Programme for at Risk Adults: a Randomized Clinical Trial

Clinical Trial Summary

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.

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06262464
Study type Interventional
Source Babes-Bolyai University
Contact Roxana Cardo?, PhD
Phone 0040751477323
Email roxanaoltean@psychology.ro
Status Recruiting
Phase N/A
Start date February 9, 2024
Completion date April 1, 2024
View Details
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