Clinical Trial to Reduce Perinatal Intimate Partner Violence
Recruiting
N/A
Interventional Study
Domestic Violence
Perinatal Problems
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 250 (estimated)
- Sponsor
- University of Pittsburgh · Other
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About This Trial
This is a two-armed, fully powered hybrid type 1 trial to test the effectiveness of a doula intervention compared with an active control in reducing intimate partner violence (IPV) among perinatal IPV survivors
Trial Locations
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Eligibility Criteria
Inclusion Criteria: Perinatal IPV survivors are eligible if they:
* 1\) feel comfortable completing the study in Spanish or English
* 2\) are age 18 or older
* 3\) are no more than 24 weeks 6 days gestation (note: participants enrolled earliest at 18 weeks, baseline at 22 weeks with a 3 week window…
Contacts