Remote Postpartum Blood Pressure Monitoring and Cardiovascular Education
Recruiting
N/A
Interventional Study
Pre-Eclampsia; Complicating Pregnancy
Gestational Hypertension
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 296 (estimated)
- Sponsor
- Ochsner Health System · Other
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About This Trial
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 s…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. Age of at least 18 years.
2. Postpartum status.
3. Experience new-onset hypertension during pregnancy.
4. Enrollment in Connected MOM.
5. Ability to provide informed consent.
6. Establish medical care within the Ochsner System to facilitate data collection.
Exclusion Criteri…
Contacts