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NCT Number: NCT06245057

Enriched Holistic Care to Eradicate Disparities in Maternal Morbidity

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.

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Key information

Conditions

Age range

16 year–55 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Hospital of the University of Pennsylvania, Phialdelphia, Pennsylvania, United States

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About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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)

Treatment and study plan

Maternity care home model (MCHM)

Other

The maternity care home model is defined as office based prenatal care integrated with comprehensive social services.

Primary outcomes

  1. Severe Maternal Morbidity (SMM)

    Time frame: 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

Secondary outcomes

  1. Obstetric outcomes: Mode of delivery

    Time frame: At delivery

    Vaginal or cesarean

  2. Obstetric outcomes: Preterm birth less than 37 weeks

    Time frame: At delivery

    Preterm delivery defined as less than 37 weeks

  3. Obstetric outcomes: Preterm birth less than 34 weeks

    Time frame: At delivery

    Preterm delivery defined as less than 34 weeks.

  4. Obstetric outcomes: Hypertensive disorders of pregnancy

    Time frame: During pregnancy through 6 weeks postpartum

    Diagnosis of Gestational hypertension, preeclampsia with or without severe features

  5. Composite adverse neonatal outcome

    Time frame: From birth until 4 months after birth

    Made up of one or more of the following: severe respiratory distress syndrome, Culture proven/presumed neonatal sepsis, Neonatal blood transfusion, Hypoxic ischemic encephalopathy, Intraventricular hemorrhage grade 3 or 4, Necrotizing enterocolitis, Need for head cooling,

  6. Postpartum visit attendance

    Time frame: From delivery discharge up to 12 weeks postpartum

    Whether or not the patient attended their routine postpartum visit up to 12 weeks postpartum mark.

  7. Edinburgh Postnatal Depression Scale (EPDS) Screening

    Time frame: At delivery and at 3-6 months postpartum

    Scores from the validated EPDS screening tool will be calculated using standard scoring criteria for each of the 10 items. A score of 9 or greater or indication of suicide ideation will be used to indicate a positive depression screen

  8. Unscheduled Emergency room/pregnancy triage visits

    Time frame: Post-randomization to 1 year postpartum

    Record number of unscheduled visits, reason for visit, whether or not patient was admitted to hospital.

  9. Perceived stress scale

    Time frame: Post-randomization to 1 year postpartum

    Scores from the validated Perceived Stress Scale (PSS-4) will be calculated using standard scoring criteria for each of the 4 items. Higher scores are correlated with more perceived stress.

    Survey to be completed at randomization, at delivery, at 3 months post partum, and at 1 year post partum.

  10. Person centered prenatal care survey for people of color

    Time frame: After delivery up to 6 weeks postpartum

    Scores from this 34-item scale will be calculated using standard scoring criteria. This scale measures person-centered prenatal care that reflects the experiences of people of color.

  11. Rate of Lactation initiation and continuation

    Time frame: From delivery through 1 year postpartum

    Initiation of breastfeeding; Continuation of breastfeeding through 1 year postpartum. To be assessed by EMR documentation and patient report at 3-months and 1 year postpartum.

  12. Perceived discrimination

    Time frame: At randomization

    Perceived discrimination will be assessed using the Experiences of Discrimination measure (Krieger et al, 2005). The measure lists 9 situations in which respondent may have experienced racial discrimination. Responses options are Yes/No. It is scored by counting the number of situations in which participant reported experiencing racial discrimination. Score ranges from 0 to 9, higher being more experiences of discrimination.

  13. Birth satisfaction (BSS-R survey)

    Time frame: After delivery up to 6 weeks postpartum

    Patient satisfaction as measured by the BSS-R with a possible score of 0-40 with 0 equaling the least birth satisfaction

Study contacts

Contact information is provided by the study sponsor or research team.

Elizabeth Norton, MPH, MBE

CONTACT

[email protected]

215-349-5277

Sindhu K Srinivas, MD, MSCE

CONTACT

[email protected]

215-662-2982

Sponsors and collaborators

Lead sponsor

University of Pennsylvania

Other

Collaborators

  • National Institute of Nursing Research (NINR)

Registry information

Official study title

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

Acronym: ENHANCED

Important dates

Study start
2024
Primary completion
2028
Study completion
2028
First posted
Feb 7, 2024
Registry last updated
Apr 21, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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