Clinical trial Recruiting at 1 site Interventional Ages 18 and up Women only

Community health worker coaching to lower heart risk after a hypertensive pregnancy

Official title: Community Health Worker Coaching to Reduce CVD Disease Risk Among Women After a Hypertensive Disorder of Pregnancy

Run by University of South Carolina · NCT07457970 · Data updated 2026-11-12

This program tests whether adding community health worker–led lifestyle coaching to remote blood pressure monitoring helps women who had high blood pressure during pregnancy better control blood pressure and lower heart disease risk.

More Pregnancy trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexWomen only
Enrollment240 (estimated)
SponsorUniversity of South Carolina
Academic / other
Locations1 site (Columbia, South Carolina)
StatusRecruiting
StartedApril 24, 2026
Main results expectedJuly 15, 2029
Study endsJuly 15, 2029
Registry record updatedMay 4, 2026
Trial IDNCT07457970 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are pregnant women at or after 28 weeks with a current or prior hypertensive disorder of pregnancy or chronic hypertension, carrying a single fetus, with phone access and plans to deliver at Prisma Health-Midlands Hospital.

Probably not a fit

Women with multiple gestations, major fetal anomalies, who do not speak English, or who delivered more than 14 days earlier are excluded and would not be eligible to benefit from this program.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The study will enroll 240 pregnant women from 28 weeks gestation through delivery who have current or prior hypertensive disorders of pregnancy or chronic hypertension and a singleton pregnancy. All participants receive an automated blood pressure cuff with remote monitoring for the first 6 weeks postpartum, with daily checks initially and reduced frequency through week 6; readings flow into the electronic medical record and nurses follow up on missed or concerning values. The enhanced-care arm adds a community health worker–led lifestyle coaching program beginning after the initial monitoring period to address weight, diet, activity, and mental well-being. Primary outcomes include blood pressure control and average resting blood pressure by 6 months postpartum, with secondary outcomes including weight, diet and activity measures, mental health, and emergency visits or readmissions.

Why it matters

Potential benefit: If successful, the combined remote monitoring and community health worker coaching could help postpartum women achieve better blood pressure control and reduce longer-term cardiovascular risk.

How similar studies have gone: Remote blood pressure monitoring has shown benefit for postpartum hypertension and community health worker lifestyle programs have improved cardiovascular risk factors in other populations, but combining these approaches in the postpartum hypertensive population is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* 28 weeks gestation
* A current hypertensive disorders in pregnancy or chronic hypertension
* Singletons
* Access to phone
* Plan to deliver at Prisma Health-Midlands Hospital.

Exclusion Criteria:

* Multiples
* Fetal anomaly
* Don't speak English
* Already delivered a baby greater than 14 days ago.

Where it's running

  • University of South Carolina
    Columbia, South Carolina, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.