Sign in

NCT07356518Recruiting

Telehealth and Remote Blood Pressure

Feasibility and Safety of Incorporating Telehealth Visits Combined With Remote Blood Pressure Monitoring in the Management of Chronic Hypertension in Pregnancy

Source: ClinicalTrials.gov · Last updated 27 Apr 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
12 Jan 2026
Start date
22 Apr 2026
Primary completion date
Dec 2026
Lead sponsor
Wake Forest University Health Sciences
NCT number
NCT07356518

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From 22 Apr 2026 to the primary completion date, Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Participation in another study without prior approval
  • Prior stroke

Other illness

  • Any significant chronic medical or psychiatric illness that, in the investigator's opinion, would prevent participation in the study
  • Cardiac disorders: cardiomyopathy, angina, Coronary Artery Disease (CAD)
  • Current substance abuse disorder
  • Severe hypertension

Other

  • Multifetal pregnancy
  • Plan to deliver outside Atrium Health Wake Forest Baptist
  • Suspected or known fetal major structural/chromosomal abnormality or fetal demise

Who the study is looking for

  • prior diagnosis of Chronic hypertension (cHTN)
  • Pregnant women
  • Known: documented diagnosis or on antihypertensive medication prior to pregnancy

Age in the registry: 18 years to 45 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Wake Forest University Health Sciences
Coordinator of this site? Confirm its status
Winston-SalemUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.