跳至主要内容
临床试验/NCT06245057
NCT06245057招募中不适用

The ENHANCED Trial: Enriched Holistic Care to Eradicate Disparities in Maternal Morbidity

University of Pennsylvania4 个研究点 分布在 1 个国家目标入组 2,300 人开始时间: 2024年1月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
2,300
试验地点
4
主要终点
Severe Maternal Morbidity (SMM)

研究概览

简要总结

The goal of this randomized controlled intervention trial is to evaluate an integrated, interdisciplinary, multi-level maternity care home model (MCHM) aimed at reducing severe maternal morbidity (SMM) among a group of Black indigenous and people of color (BIPOC) patients.

The main question it aims to answer is whether a patient-centered MCHM will address the gap in social, structural, and health system factors that contribute to disparities for the most vulnerable patients, thereby reducing SMM.

Participants will be randomized to a MCHM (office-based prenatal care that is integrated with social services within the MCHM) or standard of care (office-based prenatal care with individually outsourced social services referrals) and followed during pregnancy through 1 year postpartum.

详细描述

This randomized controlled trial addresses social and structural inequities to reduce severe maternal morbidity (SMM) and maternal mortality in the most at-risk patients - those that self-identify as Black, indigenous and people of color (BIPOC). Specifically, the intervention will implement and evaluate an integrated, multi-level maternity care home model (MCHM) that incorporates maternity care navigation, benefits navigation, social work, doula and mental health resources all within one care-delivery model. While previous studies have evaluated single social determinants (e.g. education and insurance) or single solutions (e.g. care navigator), these approaches lack a comprehensive, integrated approach that is responsive to all patient needs.

The study will test the central hypothesis that a patient-centered MCHM will address the gap in social, structural, and health system factors that contribute to disparities for the most vulnerable BIPOC patients, thereby reducing SMM. To test the effectiveness of this MCHM and ensure timely uptake of the results, the investigators propose a type 1 hybrid effectiveness-implementation trial to evaluate the effectiveness and implementation of an integrated MCHM that provides a comprehensive approach by partnering a unified model of social and structural service delivery with medical service delivery in all prenatal offices affiliated with the two largest birthing hospitals in Philadelphia.

Within this study, the investigators will determine the effectiveness of an integrated MCHM in reducing SMM among BIPOC patients (Aim 1). Patients will be randomized (n=2300) to a MCHM (office-based prenatal care that is integrated with social services within the MCHM) or standard of care (office-based prenatal care with individually outsourced social services referrals) and followed throughout pregnancy and for 1 year postpartum. To determine mechanisms by which this integrated MCHM impacts SMM (Sub-Aim 1a), the investigators will evaluate numerous factors that could plausibly mitigate the effects of health system failures, provider bias and adverse social conditions (e.g. improved health system access, care coordination). The investigators will also characterize patient, provider and organizational implementation determinants relevant to an integrated MCHM and identify barriers and facilitators to implementation and sustainability (Aim 2) as well as determine resource utilization and total cost/cost savings associated with the MCHM (Sub-Aim 2a) by partnering with commercial and Medicaid payers.

Importantly, the results of the proposed study will provide actionable evidence to support effective maternity care delivery that results in optimal and equitable outcomes, thereby revolutionizing the way in which prenatal, intrapartum and postpartum care is delivered and experienced. Additionally, even if the trial is negative in reducing SMM, there are still numerous other potential benefits to an integrated MCHM (including many of the secondary outcomes being evaluated) and the investigators will have therefore collected valuable information to inform the implementation of this model into clinical practice.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
16 Years 至 55 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

  • Pregnant patients who self-identify as Black, Indigenous, Asian, or Latina (BIPOC)
  • Ages 16-55
  • Presentation to the hospital in pregnancy - this includes prenatal care or the emergency department
  • Plan to deliver at the 2 Penn hospital sites
  • Patients must be able to read and understand English or Spanish
  • Participants must be willing and able to sign the informed consent form

排除标准

  • Unable to provide written consent by being unable to read or sign informed consent.
  • Enrolled in ENHANCED Trial in a prior pregnancy
  • Already participating in Maternity Care Home Model (MCHM)

研究组 & 干预措施

Maternity care home model (MCHM)

Experimental

Office based prenatal care integrated with comprehensive social services within the maternity care home model.

干预措施: Maternity care home model (MCHM) (Other)

Usual care arm

No Intervention

Office based prenatal care with individually outsourced social service referrals.

结局指标

主要结局

Severe Maternal Morbidity (SMM)

时间窗: Delivery to one year postpartum

The CDC definition of SMM. We will also include postpartum hemorrhage, infection, thrombosis, readmission and maternal mortality within this definition

次要结局

  • Obstetric outcomes: Mode of delivery(At delivery)
  • Obstetric outcomes: Preterm birth less than 37 weeks(At delivery)
  • Obstetric outcomes: Hypertensive disorders of pregnancy(During pregnancy through 6 weeks postpartum)
  • Composite adverse neonatal outcome(From birth until 4 months after birth)
  • Perceived stress scale(Post-randomization to 1 year postpartum)
  • Person centered prenatal care survey for people of color(After delivery up to 6 weeks postpartum)
  • Rate of Lactation initiation and continuation(From delivery through 1 year postpartum)
  • Perceived discrimination(At randomization)
  • Birth satisfaction (BSS-R survey)(After delivery up to 6 weeks postpartum)
  • Obstetric outcomes: Preterm birth less than 34 weeks(At delivery)
  • Postpartum visit attendance(From delivery discharge up to 12 weeks postpartum)
  • Edinburgh Postnatal Depression Scale (EPDS) Screening(At delivery and at 3-6 months postpartum)
  • Unscheduled Emergency room/pregnancy triage visits(Post-randomization to 1 year postpartum)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Sindhu Srinivas, MD

Vice Chair for Quality and Safety, Department OBGYN

University of Pennsylvania

研究点 (4)

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