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
Supportive Care
Participants needed
240 (estimated)
Sponsor
University of South Carolina · Other
Who this trial is looking for
This trial is looking for women who are currently pregnant and have high blood pressure. Participants will use a phone to monitor their blood pressure and join a lifestyle program with support from a community health worker.
Are You a Good Fit for This Trial?
You may be able to join if
I am at least 28 weeks pregnant.
I have high blood pressure related to pregnancy or chronic hypertension.
I am expecting one baby.
I have access to a phone.
I plan to deliver at Prisma Health-Midlands Hospital.
You may not be able to join if
I am pregnant with more than one baby.
I have a fetal anomaly.
I do not speak English.
I have already delivered a baby more than 14 days ago.
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.
The goal of this clinical trial is to find out whether an enhanced program works better than remote blood pressure monitoring (RBPM) alone for women who had high blood pressure during pregnancy. The enhanced program combines RBPM with a lifestyle program led by a community health worker (CHW).
The study will examine whether the enhanced program helps women better control their blood pressure, low…
The goal of this clinical trial is to find out whether an enhanced program works better than remote blood pressure monitoring (RBPM) alone for women who had high blood pressure during pregnancy. The enhanced program combines RBPM with a lifestyle program led by a community health worker (CHW).
The study will examine whether the enhanced program helps women better control their blood pressure, lowers their average resting blood pressure, improves heart health risk factors (such as weight, diet, physical activity), supports mental well-being, and reduces emergency department visits and hospital readmissions by 6 months after delivery.
Trial Locations
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Eligibility 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 gr…
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.
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