Timely Detection and Management of Postpartum Hypertension

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.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Female
Study type
Interventional
Purpose
Prevention
Participants needed
6,030 (estimated)
Sponsor
Yale University · Other
Who this trial is looking for

This trial is looking for women who have recently given birth and may experience high blood pressure after delivery. Participants will receive different care approaches to help detect and manage postpartum hypertension and related health issues.

Are You a Good Fit for This Trial?
Rules you out Primary psychotic disorder

You may be able to join if

  • I have given birth to one baby.
  • I am postpartum.
  • I speak English or Spanish.
  • My pregnancy was at least 24 weeks along.
  • I have Medicaid or similar insurance, or I am uninsured.
  • I live in Connecticut, Massachusetts, or New York.

You may not be able to join if

  • I am pregnant with more than one baby.
  • I had a pregnancy that was less than 24 weeks.
  • I have a serious fetal problem or experience stillbirth.
  • I am actively using illegal drugs.
  • I have thoughts of harming myself.
  • I have a serious mental health condition like schizophrenia.
  • I plan to move out of state within 6 months.
  • I cannot give consent.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

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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