Mode
Text Size
Log in / Sign up
N/A N=120 Randomized Triple-blind Prevention

App-based Remote Blood Pressure Monitoring

Gestational Hypertension · Preeclampsia · Chronic Hypertension Complicating Pregnancy

Enrolled (actual)
120
Serious AEs
0.0%
Results posted
Feb 2025
Primary outcome: Primary: Blood Pressure Ascertainment — 40; 39 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
App-based remote blood pressure monitoring (Behavioral); text-message based remote blood pressure monitoring (Behavioral)
Age
Adult · 18+ yrs
Sex
Female
Sponsor
Women and Infants Hospital of Rhode Island
Primary completion
Jun 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Blood Pressure Ascertainment
40; 39
SECONDARY
Postpartum Readmission for Hypertension or Preeclampsia
4; 8
SECONDARY
Adherence to Evidence-based Practice
15; 16
SECONDARY
Postpartum Severe Maternal Morbidity Composite
0; 0
SECONDARY
"Using Any Number From 0 to 10 Where 0 is the Worst Possible Experience and 10 is the Best Possible Experience, Please Rate Your Experience in the Postpartum Hypertension Program"
10; 10
SECONDARY
Decisional Regret Scale
5; 0

Summary

Remote postpartum blood pressure monitoring program with text messages has been shown to increase adherence to recommended postpartum blood pressure checks among those with hypertension at discharge from birth hospitalization, but these programs require medically trained professionals to respond to each individual text message. A bluetooth-enabled blood pressure cuff that synchs automatically a smartphone application that leverages Artificial Intelligence to provide tailored recommendations based on recorded blood pressure measurements--and can also provide on-demand education on hypertension--may be less costly way to provide similar support.

Eligibility Criteria

Inclusion Criteria

  • a) English- or Spanish-speaking
  • b) maternal age >18 years old
  • c) smartphone ownership for remote blood pressure ascertainment
  • d) diagnosis of gestational hypertension, preeclampsia, or chronic hypertension at hospital discharge
  • e) plan to receive postpartum care at a Women & Infants Hospital (WIH)-affiliated clinic

Exclusion Criteria

  • a) fetal anomaly
  • b) prisoners
  • c) lack of smartphone
  • d) inability to consent.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05595629). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search