Randomized Controlled Trial of Two Mobile Health Strategies to Manage Postpartum Hypertension

Part of paid clinical trials in New York, New York.

Sponsor
Jennifer Lewey, MD, MPH
Study ID
NCT07209254
Status
Recruiting

Conditions

  • Hypertension, Pregnancy Induced

Eligibility Criteria

Sex
FEMALE
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • High-touch blood pressure management — OTHER
    Twelve weeks of text-based home blood pressure monitoring with BP self-management and team-based care
  • Low-touch blood pressure management — OTHER
    10 days of text-based home blood pressure monitoring

Study Details

A multicenter randomized trial that will compare the effectiveness of two postpartum blood pressure (BP) management strategies in improving blood pressure and cardiac function and increasing patient engagement and feeling of control over one's health

Key Dates

Start date
Mar 2, 2026
Status verified
Apr 2026
Primary completion
Oct 31, 2029
Completion
Nov 30, 2029

Study Design

Enrollment
770 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: High-touch blood pressure management
  • Experimental: Low-touch blood pressure management

Primary Outcome Measure

Mean diastolic blood pressure (DBP) [ Time Frame: 12 months postpartum ]

Central Contacts

Locations (3)

FacilityCityStateZIPSite coordinators
NYU Langone HealthNew YorkNew York10022
Christina Penfield, MD, MPH
(646)-754-2700
Michelle Rojas
(646) 679-0737
Christina Penfield, MD, MPH (PRINCIPAL_INVESTIGATOR)
Harmony Reynolds, MD (PRINCIPAL_INVESTIGATOR)
The Ohio State UniversityColumbusOhio43210
Anna Bartholomew, MPH, BSN, RN
614-685-3229
Maged Costantine, MD (PRINCIPAL_INVESTIGATOR)
University of PennsylvaniaPhiladelphiaPennsylvania19104
Alexis Giron, M.S
215-275-2507
Meaghan McCabe, MPH
Jennifer Lewey, MD, MPH (PRINCIPAL_INVESTIGATOR)
Lisa D Levine, MD, MSCE (PRINCIPAL_INVESTIGATOR)

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