Project EMPOWER-OCD

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorBoston University Charles River Campus

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

Treatment groups

110 Participants
are divided into 2 treatment groups