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
Diagnostic
Participants needed
400 (estimated)
Sponsor
University of Minnesota · Other
Who this trial is looking for
This trial is looking for women who have had high blood pressure during pregnancy. Participants will monitor their blood pressure remotely for a specific period after giving birth to help understand how long this should last for the best health outcomes.
Are You a Good Fit for This Trial?
You may be able to join if
I am 18 years or older
I have been discharged after delivery at University of Minnesota Medical Center
I am enrolled in the HOPE-BP Program
You may not be able to join if
I am taking blood pressure medication at 2 weeks postpartum
I have a medical condition that makes randomization not appropriate
I have opted out of clinical research
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.
Postpartum remote blood pressure monitoring programs for patients with hypertensive disorders of pregnancy (HDP) are becoming part of standard postpartum management. Existing programs range in duration from 2 to 6 weeks but there has not been any evaluation as to what program duration is optimal. The primary objective of this study is to evaluate the impact of program duration on clinical outcomes…
Postpartum remote blood pressure monitoring programs for patients with hypertensive disorders of pregnancy (HDP) are becoming part of standard postpartum management. Existing programs range in duration from 2 to 6 weeks but there has not been any evaluation as to what program duration is optimal. The primary objective of this study is to evaluate the impact of program duration on clinical outcomes for patients participating in a single institution's postpartum remote blood pressure monitoring program for patients with HDP.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 18 years or older
* Discharged after delivery at University of Minnesota Medical Center
* Enrolled into the HOPE-BP Program
Exclusion Criteria:
* Ongoing antihypertensive medication use at 2 weeks (time of randomization)
* Have a medical comorbidity that would not be clinica…
Inclusion Criteria:
* 18 years or older
* Discharged after delivery at University of Minnesota Medical Center
* Enrolled into the HOPE-BP Program
Exclusion Criteria:
* Ongoing antihypertensive medication use at 2 weeks (time of randomization)
* Have a medical comorbidity that would not be clinically appropriate to randomize
* Patients opted out of clinical research
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