NCT06920563Recruiting
Remote Postpartum Blood Pressure Monitoring and Cardiovascular Education
Remote Postpartum Blood Pressure Monitoring and Cardiovascular Education to Reduce Emergency Department Visits, Re-admissions and Adverse Cardiovascular Outcomes in Hypertensive Disorder of Pregnancy
Source: ClinicalTrials.gov · Last updated 9 Apr 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
The goal of this clinical trial is to learn if patient education and regular text reminders are a feasible intervention to engage patients and reduce post partum hypertension. The main questions it aims to answer are: Is a structured postpartum remote blood pressure monitoring intervention with education and individualized medication initiation/adjustment follow-up by televisit feasible? Does a structured program reduce the occurrence of postpartum hypertension, ED visits, hospital readmissions, and adverse outcomes? Participants will: View an educational video on HDP post-delivery Receive 1-2 times daily text messages for 6 weeks postpartum Have their blood pressure medications adjusted to lower targets post partum
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 296 (estimated)
- First submitted
- 25 Mar 2025
- Start date
- 17 Mar 2025
- Primary completion date
- 16 Oct 2026
- Lead sponsor
- Ochsner Health System
- Diseases
- High blood pressure
- NCT number
- NCT06920563
What you commit to
- Study type: Interventional
- Planned participants: 296
- From 17 Mar 2025 to the primary completion date, 16 Oct 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
- History of preeclampsia or gestational hypertension during previous pregnancy
Other illness
- History of chronic hypertension
- History of coronary artery disease (myocardial infarction, coronary stent placement, coronary artery bypass grafting, spontaneous coronary artery dissection)
- History of ischemic CVA
- History of Congestive heart failure
- Congenital heart disease
Other
- Renal dysfunction
- Liver dysfunction
- Left ventricular dysfunction
- Still birth at delivery
Who the study is looking for
- Age of at least 18 years.
- Postpartum status.
- Experience new-onset hypertension during pregnancy.
- Enrollment in Connected MOM.
- Ability to provide informed consent.
- Establish medical care within the Ochsner System to facilitate data collection.
Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Ochsner Baptist Coordinator of this site? Confirm its status | New Orleans | United States | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.