Clinical Trials Directory

Trials / Completed

CompletedNCT03185455

Remote Surveillance of Postpartum Hypertension

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
206 (actual)
Sponsor
University of Pennsylvania · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

Women with hypertensive disorders of pregnancy need postpartum blood pressure (BP) surveillance to detect persistent hypertension. Various barriers result in only 30% attendance at postpartum BP visits. A more effective strategy is needed. Women with hypertension of pregnancy will be randomized to either text-based monitoring or office visits. Those randomized to the intervention will receive a BP cuff and text in their BP to an automated, clinician derived, HIPAA compliant text-based algorithm.

Detailed description

Hypertension is a leading cause of maternal morbidity, mortality and obstetrical readmissions. Peak blood pressure usually occurs 3-6 days postpartum, and is typically unaccompanied by warning symptoms. Although there is a clear need for effective and reliable blood pressure surveillance after delivery, there are significant obstacles to in-person visits in the immediate postpartum period, including sleep deprivation, newborn care, and transportation needs. These barriers have proven real as we observed only 30-50% attendance to office blood pressure visits following delivery. This proposal will investigate whether text-based communication between patients and providers is an effective alternative method for monitoring postpartum hypertension in at risk women. Women with hypertensive disorders of pregnancy with access to a cell phone with unlimited text message capabilities will be randomized to either office visit blood pressure checks after discharge or receive a blood pressure cuff and text in blood pressures for two weeks postpartum using a standardized, HIPAA compliant, physician derived automated platform.

Conditions

Interventions

TypeNameDescription
OTHERRemote (text based) surveillanceWomen with hypertensive disorders of pregnancy with access to a cell phone with unlimited text message capabilities will be randomized to either office visit blood pressure checks after discharge or receive a blood pressure cuff and text in blood pressures for two weeks postpartum using a standardized, HIPAA compliant, physician derived automated platform.

Timeline

Start date
2016-08-22
Primary completion
2017-01-20
Completion
2017-01-23
First posted
2017-06-14
Last updated
2023-04-12
Results posted
2019-06-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03185455. Inclusion in this directory is not an endorsement.