Actively Recruiting
Telehealth and Remote Blood Pressure
Led by Wake Forest University Health Sciences · Updated on 2026-04-27
60
Participants Needed
1
Research Sites
31 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this research study is to compare the management of chronic hypertension during pregnancy using telehealth visits with blood pressure telemonitoring and health coaching as compared to standard in person clinic visits. The study involves pregnant woman aged 18-45 who are receiving care for chronic hypertension. Participation in this research study will last until their baby is delivered. The number of in-person clinic visits depends on the participant's treatment assignment. Those assigned to telehealth visits will have telehealth visits alternating with clinic visits every two weeks until the end of pregnancy week 31. Those assigned to telehealth visits will also have five sessions with a health coach via telephone or video from the time of enrollment until the end of pregnancy week 36.
CONDITIONS
Official Title
Telehealth and Remote Blood Pressure
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Prior diagnosis of chronic hypertension (cHTN)
- Pregnant women
- Documented diagnosis or on antihypertensive medication prior to pregnancy
You will not qualify if you...
- Any significant chronic medical or psychiatric illness that would prevent participation
- Cardiac disorders such as cardiomyopathy, angina, or coronary artery disease (CAD)
- Current substance abuse disorder
- Multifetal pregnancy
- Participation in another study without prior approval
- Plan to deliver outside Atrium Health Wake Forest Baptist
- Prior stroke
- Severe hypertension
- Suspected or known fetal major structural or chromosomal abnormality or fetal demise
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Wake Forest University Health Sciences
Winston-Salem, North Carolina, United States, 27157
Actively Recruiting
Research Team
E
Ejiro Obioma, MBBS MMCi
CONTACT
A
Aderonke Adeniyi, MD, MS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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