[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"postpartum-hypertension\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:postpartum-hypertension":34},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,58,85,119],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":35,"overallStatus":45,"whyStopped":4,"lastUpdateSubmitDate":46,"lastUpdatePostDateStruct":47,"startDateStruct":50,"completionDateStruct":52,"leadSponsor":54,"locationsCount":57},"100652879","community-health-worker-support-to-lower-blood-pressure-after-a-pregnancy-with-high-blood-pressure-100652879",false,"NCT07778966","Community Health Worker Support to Lower Blood Pressure After a Pregnancy With High Blood Pressure","Alabama Womb to Heart Solution: A Community-Based Cardiovascular Health Intervention After Hypertension in Pregnancy","AW2H","Inclusion Criteria:\n\n* Postpartum patients with pregnancy-associated hypertension (gestational hypertension, preeclampsia, eclampsia, hypertension with superimposed preeclampsia, or HELLP syndrome) or stage 2 hypertension per ACC\u002FAHA guidelines (SBP \\>=140 mmHg or DBP \\>=90 mmHg) on two separate occasions at delivery-related hospital discharge or during the postpartum period\n* Delivered in the last six weeks at \\>=14 weeks gestational age, including pregnancy loss\n* 16-56 years old\n* Speaks and writes in English\n* Delivering at UAB Hospital\n\nExclusion Criteria:\n\n* Declines randomization\n* Does not speak English\n* Currently incarcerated\n* Currently enrolled in other community health worker studies or services","FEMALE","16 Years","56 Years",{"count":21,"type":22},174,"ESTIMATED","INTERVENTIONAL",[25],"NA","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.\n\nA 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.\n\nThe 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\u002Fphone. 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.",[28,29,30,31,32,33,34],"Pregnancy-Associated Hypertension","Gestational Hypertension","Preeclampsia","Eclampsia","HELLP Syndrome","Hypertension, Stage 2","Postpartum Hypertension",[36,37,38,39,40,41,42,43,44],"Community health worker","Postpartum","Blood pressure","Self-measured blood pressure monitoring","Cardiovascular disease prevention","Life's Essential 8","Hypertensive disorders of pregnancy","Alabama","Primary care linkage","NOT_YET_RECRUITING","2026-08-18",{"date":48,"type":49},"2026-08-21","ACTUAL",{"date":51,"type":22},"2026-08-31",{"date":53,"type":22},"2030-07-30",{"name":55,"class":56},"University of Alabama at Birmingham","OTHER",1,{"id":59,"slug":60,"hasResults":11,"nctId":61,"briefTitle":62,"officialTitle":62,"acronym":4,"eligibilityCriteria":63,"healthyVolunteers":64,"sex":17,"minAge":65,"maxAge":66,"enrollmentInfo":67,"targetDuration":4,"studyType":23,"phases":69,"briefSummary":70,"conditions":71,"keywords":4,"overallStatus":75,"whyStopped":4,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":57},"100625271","cardiometabolic-risk-in-pregnancy-and-postpartum-100625271","NCT07420465","Cardiometabolic Risk in Pregnancy and Postpartum","Inclusion Criteria:\n\n* Singleton pregnancy\n* 18 years and older\n* 3rd trimester of pregnancy at enrollment\n* Will be living in the area for the study duration\n* Women with or without pregnancy complications (e.g., gestational hypertension, preeclampsia, gestational diabetes)\n\nExclusion Criteria:\n\n* Multiple births\n* Diagnosed CVD or diabetes prior to pregnancy\n* Renal or other serious maternal diseases pre-pregnancy",true,"18 Years","45 Years",{"count":68,"type":22},200,[25],"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.",[72,34,73,74],"Hypertensive Disorders of Pregnancy","Cardiovascular Disease Risk","High Blood Pressure","RECRUITING","2026-07-14",{"date":78,"type":49},"2026-07-16",{"date":80,"type":49},"2026-04-01",{"date":82,"type":22},"2027-12",{"name":84,"class":56},"Forgive Avorgbedor",{"id":86,"slug":87,"hasResults":11,"nctId":88,"briefTitle":89,"officialTitle":90,"acronym":91,"eligibilityCriteria":92,"healthyVolunteers":11,"sex":17,"minAge":93,"maxAge":94,"enrollmentInfo":95,"targetDuration":4,"studyType":23,"phases":97,"briefSummary":98,"conditions":99,"keywords":103,"overallStatus":45,"whyStopped":4,"lastUpdateSubmitDate":110,"lastUpdatePostDateStruct":111,"startDateStruct":113,"completionDateStruct":115,"leadSponsor":117,"locationsCount":4},"100638145","community-support-and-mobile-apps-to-help-black-women-control-high-blood-pressure-after-pregnancy-100638145","NCT07606027","Community Support and Mobile Apps to Help Black Women Control High Blood Pressure After Pregnancy","Postpartum Remote Monitoring and Integration of Mobile Health With Engagement From Community Health Workers for Regulating Elevated Blood Pressure","PRIME CARE","Inclusion Criteria:\n\n* Black\u002F African American patients\n* Age: 19 and 50 years of age\n* Diagnosis: Hypertension Disorders of Pregnancy\n* Enrolled in STAMPP-HTN for first 6 weeks postpartum\n\nExclusion Criteria:\n\n* Age: \\\u003C19 years\n* Significant Kidney or Liver disease that may limit antihypertensive medication adjustment","19 Years","50 Years",{"count":96,"type":22},404,[25],"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.",[100,101,102,34],"Hypertensive Disorders of Pregnancy (HDP)","Hypertension, Pregnancy Induced","Severe Maternal Morbidity",[104,105,106,107,108,109],"Hypertension, Pregnancy-Induced","Postpartum Period","Remote Blood Pressure Monitoring","Community Health Workers","Postpartum Care","African American Women","2026-05-19",{"date":112,"type":49},"2026-05-26",{"date":114,"type":22},"2026-07-01",{"date":116,"type":22},"2031-06-30",{"name":118,"class":56},"University of Nebraska",{"id":120,"slug":121,"hasResults":11,"nctId":122,"briefTitle":123,"officialTitle":124,"acronym":4,"eligibilityCriteria":125,"healthyVolunteers":11,"sex":17,"minAge":65,"maxAge":4,"enrollmentInfo":126,"targetDuration":4,"studyType":23,"phases":128,"briefSummary":129,"conditions":130,"keywords":4,"overallStatus":75,"whyStopped":4,"lastUpdateSubmitDate":131,"lastUpdatePostDateStruct":132,"startDateStruct":134,"completionDateStruct":136,"leadSponsor":138,"locationsCount":140},"100507192","trauma-informed-approach-to-timely-detection-and-management-of-early-postpartum-hypertension-100507192","NCT05884190","Trauma-informed Approach to Timely Detection and Management of Early Postpartum Hypertension","Community-based, Family-centered, Trauma-informed Approach to Timely Detection and Management of Early Postpartum Hypertension","Inclusion Criteria:\n\n* Delivery of singleton live birth (twins reduced to singleton or with vanishing twin syndrome prior to 14 weeks qualify)\n* Postpartum\n* English or Spanish speaking\n* Viable pregnancy 24 weeks of gestation or above (Child can be in NICU to participate)\n* Medicaid or the equivalent within each state (for example, Connecticut has Husky insurance) or uninsured\n* Must living in one of the three states involved in this study (Connecticut, Massachusetts, New York) and preferably within the geographical area of each of the hospitals\n\nExclusion Criteria:\n\n* Multifetal pregnancy (since are they at increased risk for key outcomes)\n* Gestational age \\\u003C24 weeks;\n* Known major fetal anomaly in current pregnancy or stillbirth\n* Actively using illicit\u002Fillegal substances (such as cocaine, heroin and other types of illicit opiates such as fentanyl) as noted in delivery hospitalization notes\n* Active suicidal ideation with intent and plan\n* Known primary psychotic disorder (i.e. schizophrenia, or schizoaffective disorder)\n* Plans to move out of the state within 6 months\n* Incapable of consent\n* Severe medical complications that don't allow a mother to do the study effectively (for example, active treatment for cancer, dialysis etc. )\n* Physician or provider refusal\n* Patient refusal\n* Incarcerated or institutionalized\n* Stillbirth\n\nBirths that result in the newborn being under the care of another person or institution other than the birthing individual (e.g. adoption, state involvement) will be evaluated on an individual basis to determine if that person should be included.\n\nFor participants without access to a phone, we will explore if there are options that will allow them to have access to a devise for the times when they need to communicate with the study team. If not, they will not be able to participate in the study since this study requires phone or telehealth communication with research staff and\u002For APPs, and CHWs depending on study phase.",{"count":127,"type":22},6030,[25],"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.",[34],"2025-04-07",{"date":133,"type":49},"2025-04-09",{"date":135,"type":49},"2023-06-12",{"date":137,"type":22},"2027-10",{"name":139,"class":56},"Yale University",3]