EligibleTrials

An OCD Prevention Programme for at Risk Adults

Recruiting · NCT06262464 · Interventional (participants receive a specific treatment) · Lead sponsor: Babes-Bolyai University

View the official record on ClinicalTrials.gov →
Anxiety

Interventions studied

Prevention

What this trial is about

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.

Who can take part

Age range
18 Years to 65 Years
Sex
All (male and female)
Healthy volunteers
Yes - healthy volunteers may be accepted
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)

Inclusion criteria

Exclusion criteria

Where it is running

1 location listed.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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