CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 206 enrolled
Drug / intervention
Remote (text based) surveillanceother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03185455
NCT03185455N/ACompleted

Remote Surveillance of Postpartum Hypertension

University of Pennsylvania·interventional·Posted Jun 14, 2017·Updated Apr 12, 2023

In Brief

A clinical study evaluating Remote (text based) surveillance for Hypertension in Pregnancy. Completed, enrolled 206 participants across 1 site.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
2017201820192020202120222023202420252026
First PostedJun 14, 2017
Enrollment StartAug 22, 2016
Primary CompletionJan 20, 2017
Study CompletionJan 23, 2017
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 9.0 years ago

Interventions

Remote (text based) surveillanceother

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.