About this trial
This research study aims to adapt and evaluate the acceptability and effectiveness of Project EMPOWER-OCD for socioeconomically diverse caregivers of patients with OCD. Designed to reduce obstacles (e.g. months long time commitment, high cost, transportation) to treatment that caregivers may be particularly prone to, project EMPOWER-OCD will provide targeted intervention of accommodation - a well-established, potentially modifiable risk factor for child anxiety, OCD, and its related disorders - in a single, self-guided session via an online format.
Eligibility criteria
Qualifiers
be a caregiver for at least one individual with OCD, defined as living in the same household and providing daily care
be 18 years old or older
the individual they are caring for have clinically significant OCD symptoms, indicated by a score a 16 or above on the self-reported Children's Yale-Brown Obsessive Compulsive Scale - Parent Report (CY-BOCS-PR)
speak, read, and write English
Disqualifiers
does not speak English
younger than 18 years old
participation in concurrent family-based CBT treatment for the patient's OCD.
Trial design
Treatments tested in this trial
- Project EMPOWER-OCD
- Project CARE