Actively Recruiting
Remote Postpartum Blood Pressure Monitoring and Cardiovascular Education
Led by Ochsner Health System · Updated on 2025-04-09
296
Participants Needed
1
Research Sites
82 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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
CONDITIONS
Official Title
Remote Postpartum Blood Pressure Monitoring and Cardiovascular Education
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age of at least 18 years
- Currently postpartum
- New-onset hypertension during this pregnancy
- Enrollment in Connected MOM
- Ability to provide informed consent
- Established medical care within the Ochsner System for data collection
You will not qualify if you...
- History of preeclampsia or gestational hypertension in previous pregnancies
- History of chronic hypertension
- History of coronary artery disease (including myocardial infarction, stent placement, bypass surgery, or spontaneous dissection)
- History of ischemic stroke
- History of congestive heart failure
- Renal dysfunction
- Liver dysfunction
- Left ventricular dysfunction
- Congenital heart disease
- Experience of stillbirth at delivery
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Ochsner Baptist
New Orleans, Louisiana, United States, 70115
Actively Recruiting
Research Team
S
Salima Qamruddin, MD
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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