Trauma-informed Approach to Timely Detection and Management of Early Postpartum Hypertension

Recruiting N/A Interventional Study
Postpartum Hypertension
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Female
Study type
Interventional
Purpose
Prevention
Participants needed
6,030 (estimated)
Sponsor
Yale University · Other
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About This Trial
The investigators primary project goal is to improve clinical outcomes, including mental health outcomes, among postpartum at-risk women experiencing health disparities by increasing awareness, detection, and timely care of postpartum hypertension, mental health and cardiovascular complications. The investigators will accomplish this by comparing the effectiveness of two multi-component multi-leve…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Delivery of singleton live birth (twins reduced to singleton or with vanishing twin syndrome prior to 14 weeks qualify) * Postpartum * English or Spanish speaking * Viable pregnancy 24 weeks of gestation or above (Child can be in NICU to participate) * Medicaid or the equivale…
Contacts

Rafael Pérez-Escamilla, PhD

8608052502

rafael.perez-escamilla@yale.edu

CONTACT