An OCD Prevention Programme for at Risk Adults

Sponsor
Babes-Bolyai University
Study ID
NCT06262464
Status
Recruiting
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Conditions

  • Obsessive-Compulsive Disorder

Eligibility Criteria

Sex
ALL
Age
18 Years - 65 Years
Healthy Volunteers
Accepted

Interventions

  • Prevention — BEHAVIORAL
    A cognitive-behavioural prevention programme.

Study Details

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.

Key Dates

First listed
Feb 16, 2024
Start date
Feb 9, 2024
Status verified
Mar 2025
Primary completion
Jul 31, 2025
Completion
Dec 31, 2025

Study Design

Enrollment
200 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION

Arms

  • Experimental: Prevention
    6 group, online sessions over two weeks. A prevention program using cognitive and behavioral strategies to reduce OCD risk factors and related symptoms.
  • No Intervention: Control
    Treatment as Usual

Primary Outcome Measure

Change from baseline in OCD symptoms on the OCI-R after the intervention [ Time Frame: Baseline and Week 2 ]

Central Contacts

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