No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Female
Study type
Interventional
Purpose
Treatment
Participants needed
296 (estimated)
Sponsor
Ochsner Health System · Other
Who this trial is looking for
This trial is looking for new mothers who had high blood pressure during pregnancy. Participants will watch educational videos, receive text reminders, and have their blood pressure medications adjusted after delivery.
Are You a Good Fit for This Trial?
You may be able to join if
I am at least 18 years old.
I am postpartum.
I experienced high blood pressure during my pregnancy.
I am enrolled in Connected MOM.
I can provide informed consent.
I have established medical care within the Ochsner System.
You may not be able to join if
I have a history of preeclampsia or gestational hypertension in a previous pregnancy.
I have a history of chronic hypertension.
I have a history of coronary artery disease.
I have a history of ischemic stroke.
I have a history of congestive heart failure.
I have renal dysfunction.
I have liver dysfunction.
I have congenital heart disease.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.
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…
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
Trial Locations
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City
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Status
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…
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 Criteria:
1. History of preeclampsia or gestational hypertension during previous pregnancy
2. History of chronic hypertension
3. History of coronary artery disease (myocardial infarction, coronary stent placement, coronary artery bypass grafting, spontaneous coronary artery dissection)
4. History of ischemic CVA
5. History of Congestive heart failure
6. Renal dysfunction
7. Liver dysfunction
8. Left ventricular dysfunction
9. Congenital heart disease
10. Still birth at delivery
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