Trials / Recruiting
RecruitingNCT06262464
An OCD Prevention Programme for at Risk Adults
The Efficacy of an OCD Prevention Programme for at Risk Adults: a Randomized Clinical Trial
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 200 (estimated)
- Sponsor
- Babes-Bolyai University · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Accepted
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.
Detailed 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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| BEHAVIORAL | Prevention | A cognitive-behavioural prevention programme. |
Timeline
- Start date
- 2024-02-09
- Primary completion
- 2025-07-31
- Completion
- 2025-12-31
- First posted
- 2024-02-16
- Last updated
- 2025-04-18
Locations
1 site across 1 country: Romania
Source: ClinicalTrials.gov record NCT06262464. Inclusion in this directory is not an endorsement.