Postpartum Hypertension

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Review clinical trials related to Postpartum Hypertension. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Community Health Worker Support to Lower Blood Pressure After a Pregnancy With High Blood Pressure

High blood pressure during or after pregnancy (such as preeclampsia, gestational hypertension, eclampsia, or HELLP syndrome) raises a mother's risk of heart disease later in life. Many patients do not return for follow-up care after delivery, missing a key window to protect their heart health. The Alabama Womb to Heart Solution (AW2H) trial will test whether pairing postpartum patients with a trained community health worker (CHW) for 6 months lowers blood pressure compared with usual care. A total of 174 postpartum patients who had pregnancy-associated hypertension or stage 2 high blood pressure will be randomly assigned (1:1) to usual care or usual care plus the AW2H CHW program. All participants receive education on measuring their own blood pressure and a pregnancy-validated home blood pressure monitor. Participants in the CHW group are also contacted regularly by a CHW for 6 months. CHWs coach home blood pressure monitoring, support taking blood pressure medications as prescribed, encourage heart-healthy habits based on the American Heart Association's Life's Essential 8, help schedule a primary care visit, provide mother-baby education (such as safe sleep and immunizations), and offer emotional support. The main outcome is systolic blood pressure 6 months after enrollment, measured at home with the study-provided monitor while a research coordinator observes in person or by video/phone. The study will also look at diastolic blood pressure and whether participants scheduled a primary care visit. Interviews and focus groups will explore participant, CHW, and provider experiences with the program.

Participants needed: 174
Trial details
Age: 16-56Biological sex: FemaleType: InterventionalSponsor: University of Alabama at BirminghamUpdated: Aug 21, 2026Locations: 1
Eligibility criteria

Postpartum patients with pregnancy-associated hypertension (gestational hyperten... [+4]

Declines randomization [+3]

Status: Recruiting

Cardiometabolic Risk in Pregnancy and Postpartum

The goal of this study is to evaluate changes in blood pressure and early cardiovascular risk markers and to determine whether a postpartum education intervention can improve cardiovascular risk monitoring among pregnant women in their third trimester through six months postpartum in Accra, Ghana. The study includes women aged 18 years and older with and without pregnancy-related cardiometabolic complications. Findings from this study will inform the development of scalable postpartum screening and intervention strategies to reduce long-term cardiovascular disease risk among women.

Participants needed: 200
Trial details
Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Forgive AvorgbedorUpdated: Jul 16, 2026Locations: 1
Eligibility criteria

Singleton pregnancy [+4]

Multiple births [+2]

Status: Not yet recruiting

Community Support and Mobile Apps to Help Black Women Control High Blood Pressure After Pregnancy

The goal of this randomized clinical trial is to evaluate the effectiveness of a collaborative care intervention, consisting of remote blood pressure monitoring and support from community health workers, in improving blood pressure control and reducing postpartum complications among Black women with hypertensive disorders of pregnancy (HDP). The primary objectives are to determine whether the intervention leads to improved blood pressure control at 12 months postpartum compared to standard care, and whether it reduces the incidence of serious maternal morbidity, including hospitalizations and cardiovascular events. Secondary objectives include examining whether patient activation and trust in the healthcare system mediate the relationship between the intervention and clinical outcomes. Participants will be enrolled at approximately 6 weeks postpartum and randomized to either the collaborative care intervention or standard postpartum care. All participants will self-monitor blood pressure using a provided device, receive guidance on hypertension management, and complete study assessments at multiple time points. Participants assigned to the intervention arm will additionally receive ongoing support from community health workers, including health education, care coordination, and assistance with healthcare navigation. Clinical outcomes and patient-reported measures will be assessed over a 12-month follow-up period.

Participants needed: 404
Trial details
Age: 19-50Biological sex: FemaleType: InterventionalSponsor: University of NebraskaUpdated: May 26, 2026
Eligibility criteria

Black/ African American patients [+3]

Age: <19 years [+1]

Status: Recruiting

Trauma-informed Approach to Timely Detection and Management of Early Postpartum Hypertension

The investigators primary project goal is to improve clinical outcomes, including mental health outcomes, among postpartum at-risk women experiencing health disparities by increasing awareness, detection, and timely care of postpartum hypertension, mental health and cardiovascular complications. The investigators will accomplish this by comparing the effectiveness of two multi-component multi-level healthcare delivery models focused on early detection and control of postpartum hypertension and the social and mental health factors known to impact maternal outcomes, with the current standard of care and with each other.

Participants needed: 6,030
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Yale UniversityUpdated: Apr 9, 2025Locations: 3
Eligibility criteria

Delivery of singleton live birth (twins reduced to singleton or with vanishing t... [+5]

Multifetal pregnancy (since are they at increased risk for key outcomes) [+12]