跳至主要内容
临床试验/NCT05499507
NCT05499507进行中(未招募)不适用

The Path to Optimal Black Maternal Heart Health: Comparing Two CVD Risk Reduction Interventions (Change of HEART)

Temple University1 个研究点 分布在 1 个国家目标入组 345 人开始时间: 2023年1月24日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
345
试验地点
1
主要终点
Change in blood pressure at 6-weeks postpartum.

研究概览

简要总结

The overarching goal of our proposal is to reduce disparities in perinatal cardiovascular disease risk factors among Black women utilizing a community-driven, social ecological framework.

详细描述

What is this research about? Heart disease (e.g., heart attack, stroke) is a major threat to safe motherhood and is the leading cause of maternal death in the United States, responsible for nearly 50 percent of pregnancy-related deaths among Black women, three times the rate of white women, and is largely preventable. It is well established that eating healthy foods and monitoring blood pressure can help prevent heart disease. While prior studies addressing these individual behaviors have led to some success, a single individual-level approach has not been enough to stop the rising rate of Black maternal mortality. Researchers have also established that depression, social isolation, and stress from racism lead to poor heart outcomes. But few studies have treated these psychosocial and structural factors in addition to individual behaviors to ensure optimal Black maternal heart health, particularly for mothers at higher risk (e.g., those with high blood pressure and/or obesity). To meet this need, the research team plans to compare two approaches that treat multiple factors leading to heart disease among patients age 18 and older who self-identify as Black or African American, have either obesity and/or high blood pressure, are less than 28 weeks pregnant, and have a smart phone. Both approaches address individual behaviors through nutrition and physical activity text messages and home blood pressure self-monitoring as well as provide training to medical care providers in order to reduce patients' experiences of racism or mistreatment. But only one of the approaches being studied also adds supports for Black women by Black women (community doula care, mental health services, and lactation consultation) during their pregnancy, birth, and postpartum in order to learn if these supports lead to lower blood pressure and also treat social isolation, depression, and increase experiences of respectful maternity care.

Who can this research help? This study will increase Black mothers' understanding of the many influences on their heart health. Findings from this study will help Black women with obesity and/or high blood pressure make informed decisions about the use of community doulas, lactation professionals, and psychotherapists as part of their care to reduce risks for heart disease during pregnancy or in the first year after their baby is born. Results may also strengthen health systems' commitment to anti-racism training as part of their efforts to provide quality health care for Black pregnant and postpartum people. And further, this research may provide evidence to insurance companies that coverage of this study's package of supports is needed.

What outcomes are being studied? The primary outcomes are changes in maternal blood pressure and body weight at six weeks and one year after giving birth. The team will also evaluate how well the treatments are implemented and able to reach patients, be adopted into practice consistently, and lead to healthcare provider and patient satisfaction. The team will analyze outcomes that patient partners have identified as important. These include perinatal mood and anxiety disorders (e.g., postpartum depression), emotional and informational support, stress, and experiences of respectful maternity care. In addition, the study team will look at clinical outcomes including if and for how long patients breastfeed, blood pressure disorders of pregnancy, how the patient gave birth (e.g., vaginal or cesarean), baby's birth weight, and how many weeks pregnant mothers were at the time of birth.

How long does this study last? Final follow-up of primary outcomes is at one year postpartum (i.e., approximately 18 months from enrollment).

How are stakeholders involved? The research team believes that efforts to improve Black maternal heart health will be most effective when partnered with patients and community leaders that have shared lived experience. Study leadership is an equitable partnership by an academic physician-researcher and community-based Black provider who herself experienced heart health complications in her pregnancy. There are three other patient investigators who will also be involved in all aspects of the planning, delivery, and evaluation of the treatments, including serving as lead doulas, therapists, and lactation professionals. Patient representatives will make up the majority of the study's advisory board to give feedback and further guide the team's efforts throughout the five years of the project. Finally, patient, health system, and community provider stakeholders will provide feedback and guidance through focus groups over the entire study duration to ensure adoption of treatments.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •age ≥18 years
  • •baseline BMI ≥30 kg/m2 and/or diagnosis of HTN (≥130/80 x 2)
  • •gestational age ≤28 weeks by last menstrual period
  • •smartphone ownership
  • •self-identification as Black or African American

排除标准

  • 未提供

研究组 & 干预措施

Change of Heart (COH)

Active Comparator

Incorporates two, evidence-based individual-level interventions (home blood pressure telemonitoring coupled with the interactive obesity treatment approach, that includes nutrition and physical activity text messages with tailored feedback) and an institutional-level intervention (anti-racism training of providers and staff along with patient feedback to inform respectful care).

干预措施: COH (Behavioral)

Change of Heart Plus (COH+)

Experimental

Includes all components of COH plus the addition of interpersonal support for Black women by Black women (community doula care, mental health services, and lactation support).

干预措施: COH+ (Behavioral)

结局指标

主要结局

Change in blood pressure at 6-weeks postpartum.

时间窗: At baseline and 6-weeks postpartum

Blood pressure will be measured at each time point on the upper arm three times at one-minute intervals after five minutes of quiet sitting. The investigators will use the validated Omron HEM-907XL and the appropriate size cuff. The investigators will average the three measures for analysis.

Change in blood pressure at 12-months postpartum.

时间窗: At baseline and 12-months postpartum

Blood pressure will be measured at each time point on the upper arm three times at one-minute intervals after five minutes of quiet sitting. The investigators will use the validated Omron HEM-907XL and the appropriate size cuff. The investigators will average the three measures for analysis.

Change in body weight at 6-weeks postpartum.

时间窗: At baseline and 6-weeks postpartum

Body weight will be measured in duplicate and recorded to the nearest 0.1kg using calibrated SECA scales at each time point.

Change in body weight at 12-months postpartum.

时间窗: At baseline and 12-months postpartum

Body weight will be measured in duplicate and recorded to the nearest 0.1kg using calibrated SECA scales at each time point.

次要结局

  • Change in emotional support at 6-weeks postpartum.(At baseline and 6-weeks postpartum)
  • Change in PMADs at 12-months postpartum.(At baseline and 12-months postpartum)
  • Obstetric mistreatment at 6-weeks postpartum(6-weeks postpartum)
  • Blood pressure control at 6-weeks postpartum for patients with hypertension (HTN) at baseline.(6-weeks postpartum)
  • Blood pressure control at 12-months postpartum for patients with hypertension at baseline.(12-months postpartum)
  • Preterm birth.(6-weeks postpartum)
  • Change in emotional support at 6-weeks postpartum.(At baseline and 6-weeks postpartum)
  • Change in emotional support at 12-months postpartum.(At baseline and 12-months postpartum)
  • Change in informational support at 6-weeks postpartum.(At baseline and 6-weeks postpartum)
  • Change in informational support at 12-months postpartum.(At baseline and 12-months postpartum)
  • Change in Perinatal Mood and Anxiety Disorders (PMADs) at 6-weeks postpartum.(At baseline and 6-weeks postpartum)
  • Change in PMADs at 12-months postpartum.(At baseline and 12-months postpartum)
  • Mothers autonomy in decision making at baseline.(Baseline)
  • Mothers autonomy in decision making at 6-weeks postpartum.(6-weeks postpartum)
  • Respectful maternity care at baseline.(Baseline)
  • Respectful maternity care at 6-weeks postpartum.(6-weeks postpartum)
  • Obstetric mistreatment at baseline.(Baseline)
  • Obstetric mistreatment at 6-weeks postpartum(6-weeks postpartum)
  • Blood pressure control at 6-weeks postpartum for patients with hypertension (HTN) at baseline.(6-weeks postpartum)
  • Blood pressure control at 12-months postpartum for patients with hypertension at baseline.(12-months postpartum)
  • Incident hypertension at 6-weeks postpartum for patients who were normotensive at baseline.(6-weeks postpartum)
  • Incident hypertension at 12-months postpartum for patients who were normotensive at baseline.(12-months postpartum)
  • Breast/Chestfeeding initiation.(6-weeks postpartum)
  • Breast/Chestfeeding duration.(12-months postpartum)
  • Breastfeeding support/self-efficacy at 6-weeks postpartum.(6-weeks postpartum)
  • Breastfeeding support/self-efficacy at 12-months postpartum.(12-months postpartum)
  • Mode of delivery.(6-weeks postpartum)
  • Infant birth weight.(6-weeks postpartum)
  • Preterm birth.(6-weeks postpartum)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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