CompletedNot Applicable

Remote BP Monitoring in the PP Period

United States213 participantsStarted 2018-11-09

Plain-language summary

The purpose of this study is to trial remote patient monitoring (RPM) in the postpartum hypertensive population in a randomized control design, with an aim to increase the number of blood pressure measurements taken during the fragile and under-monitored postpartum period and to thereby improve postpartum blood pressure control and reduce severe morbidity and mortality. The investigators plan to compare the number of blood pressures recorded in the first 10 days postpartum between patients who have been enrolled in an RPM trial to those who are being treated with the usual care.

Who can participate

Age range18 Years

SexFEMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Postpartum women * Previous diagnosis of chronic hypertension, or antepartum diagnosis of hypertensive disorder of pregnancy (defined as documented blood pressure of ≥140 systolic or ≥90 diastolic on at least 2 occasions at least 4 hours apart) * At least 18 years of age * English or Spanish speakers Exclusion Criteria: * Non-English or Spanish speakers * Women who are not planning on obtaining their postpartum follow up at CUIMC * Women who are physically unable to hold or use the tablet * Women who do not have a working phone * Provider unwilling or unable to set up escalation pathway * Women who reside outside of New York State * Hypertension diagnosed postpartum

What they're measuring

Blood Pressure (BP) Surveillance Adherence

Timeframe: Up to 14 days from delivery hospitalization discharge

Trial details

NCT IDNCT03728790

SponsorColumbia University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2019-07-28

Results submitted2020-07-24

View on ClinicalTrials.gov More Hypertensive Disorder of Pregnancy trials