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HOPE-BP 2.0: Evaluating the Optimal Duration of Postpartum Remote Blood Pressure Monitoring

University of Minnesota (UMN) logo

University of Minnesota (UMN)

Status

Enrolling

Conditions

Hypertension
Hypertensive Disorder of Pregnancy
Postpartum

Treatments

Diagnostic Test: 6-Week Home Monitoring
Diagnostic Test: 2-Week Home Monitoring

Study type

Interventional

Funder types

Other

Identifiers

NCT07204756
OBGYN-2025-34107

Details and patient eligibility

About

Postpartum remote blood pressure monitoring programs for patients with hypertensive disorders of pregnancy (HDP) are becoming part of standard postpartum management. Existing programs range in duration from 2 to 6 weeks but there has not been any evaluation as to what program duration is optimal. The primary objective of this study is to evaluate the impact of program duration on clinical outcomes for patients participating in a single institution's postpartum remote blood pressure monitoring program for patients with HDP.

Enrollment

400 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years or older
  • Discharged after delivery at University of Minnesota Medical Center
  • Enrolled into the HOPE-BP Program

Exclusion criteria

  • Ongoing antihypertensive medication use at 2 weeks (time of randomization)
  • Have a medical comorbidity that would not be clinically appropriate to randomize
  • Patients opted out of clinical research

Trial design

Primary purpose

Diagnostic

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

400 participants in 2 patient groups

2-Week Arm
Active Comparator group
Description:
Participants randomized into the 2 week arm will be immediately unenrolled from the postpartum remote blood pressure monitoring program and resume standard postpartum care
Treatment:
Diagnostic Test: 2-Week Home Monitoring
6-Week Arm
Active Comparator group
Description:
Patients randomized into the 6 week arm will continue and complete the program in its entirety per current SOC (4 additional weeks)
Treatment:
Diagnostic Test: 6-Week Home Monitoring

Trial contacts and locations

1

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Central trial contact

Erin Linden

Data sourced from clinicaltrials.gov

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