Trial results for a study investigating remote blood pressure monitoring in postpartum women with Hypertension were posted on ClinicalTrials.gov on 2026-03-02. The study, which enrolled 1607 participants, found that remote monitoring significantly increased adherence to American College of Obstetricians and Gynecologists (ACOG) blood pressure monitoring guidelines, from 30.8% in standard of care to 78.6% with remote monitoring.

Background

Hypertension, or high blood pressure, can develop in women after delivery, even if they had not experienced it during pregnancy. Untreated or undiagnosed high blood pressure in the postpartum period can lead to serious medical complications, some of which can be life-threatening. Monitoring blood pressure after childbirth is crucial for early detection and management. Remote blood pressure monitoring has been suggested as a method to improve postpartum surveillance.

Trial design

This completed study, designated as Phase NA, enrolled 1607 participants to investigate the usefulness of remote blood pressure monitoring in postpartum women with Hypertension. The trial compared remote blood pressure monitoring (rBPM) for three weeks post-discharge with standard of care (SOC) to assess its impact on monitoring adherence and other outcomes.

Key results

The trial reported several key measurements:

What this means

The results indicate that remote blood pressure monitoring significantly increased the proportion of postpartum women adhering to ACOG blood pressure monitoring guidelines, from 30.8% in standard care to 78.6% with remote monitoring. Participants in the remote monitoring group took a median of 6 measurements. The median total healthcare costs were comparable between the two groups, with 1040 US dollars for standard of care and 1046 US dollars for remote monitoring. While remote monitoring improved adherence, the data also showed varying numbers of participants experiencing at least one day with a severe hypertension event across different measurements, with some instances showing higher numbers in the remote monitoring group (e.g., 66 vs 35, 34 vs 4, 27 vs 22), which could suggest improved detection of such events due to more frequent monitoring.

Source

The information regarding these trial results was obtained from ClinicalTrials.gov, a public database of clinical studies. The results for the study NCT05236725, titled "Monitoring and Testing of Blood Pressure in Postpartum Women", were posted on 2026-03-02 on clinicaltrials.gov.