Skip to main content
OpenTrials
Recruiting

NCT Number: NCT05993689

Building TrUst and UNiting Teams Through DouLa partnErship - BUNDLE

The BUNDLE study is a prospective mixed-methods study focused on the early integration of community doula into prenatal care. The study will have three phases: Phase 1 is the qualitative phase of conducting focus groups with Black/African American (AA) birthing people and with medical and community healthcare providers to elicit feedback on how best to integrate community-based doulas and obstetricians into one united model of prenatal care to promote trust and improved maternal health outcomes. Phase 2 tests the effectiveness of the newly developed model on healthcare engagement, trust, and adverse maternal outcomes using randomized control trial of 412 Black/AA pregnant participants. Phase 3 is dissemination of BUNDLE findings in scholarly and community-based forums, including with healthcare leaders and policy makers in Wisconsin, advocating for doula coverage and health system sustainability of the integrated model.

Recruiting

Interested in participating?

Request Info

Key information

Conditions

Age range

18 year–65 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

About this study

The BUNDLE study is a prospective mixed-methods study focused on the early integration of community doula into prenatal care. The investigators will pursue the following aims using a multidisciplinary team of experts in health disparities, community engagement, qualitative research, maternal-fetal medicine, and doula support:

Aim 1: Develop an integrated prenatal care model of medical providers and community doulas in Southeastern Wisconsin Approach: The investigators will conduct six focus groups with 30 Black/AA birthing people (currently pregnant or recently postpartum) and 30 prenatal healthcare providers (obstetricians, midwives, doulas, social workers, prenatal care coordinators, nurses, mental health providers, and obstetric unit leaders) to elicit feedback on models of doula/medical provider integration with the overarching aim of building trust and improving maternal health outcomes. Focus group findings will be reviewed with a community advisory panel (CAP) developed as part of the Community Partnership of the MCW U54 center, to gain the CAP's input on intervention development.

Aim 2: Compare the effectiveness of the integrated prenatal care model to standard prenatal care in improving healthcare engagement and trust and reducing adverse maternal outcomes Approach: In a two-arm randomized controlled trial conducted at Froedtert and MCW, the investigators will randomize 412 Black/AA pregnant people to BUNDLE or standard prenatal care. Primary outcome is healthcare engagement (starting prenatal care in 1st trimester, attending at least 70% of the recommended visits, attending the postpartum visit, and receipt of recommended vaccination during pregnancy). Secondary outcomes include medical mistrust measured by trust in provider scale, perceived discrimination, and frequencies of severe maternal morbidity as defined by the Centers for Disease Control.

Aim 3: Disseminate findings to scholarly and community-based forums and actively pursue opportunities for systems- and policy-level change Approach: The investigators will disseminate findings regularly in scholarly (conference, grand rounds) and community-based (listening session, town hall) forums. The investigators will leverage the existing partnerships with policymakers, healthcare organizations, and community leaders to implement strategies to sustain successful program outcomes through policy changes at the system and statewide level by advocating for doula coverage and healthcare system sustainability of the integrated prenatal care model.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Self-reported Black or African American
  • Pregnant with singleton gestation
  • Has an established OBGY at Froedtert & the Medical College of Wisconsin (F&MCW) Health System

Exclusion criteria

  • Planning to deliver outside of F&MCW Health System
  • Receiving support beyond routing prenatal care, such as group prenatal care or has their own doula
  • Inability or unwillingness to provide informed consent

Treatment and study plan

Bundle

Other

An integrated model of community-based doulas and clinical obstetric providers

Usual Care

Other

Standard of care for pregnancy and pregnancy-related issues by the obstetric provider

Primary outcomes

  1. Perinatal Healthcare Engagement

    Time frame: From study enrollment and until 12 months postpartum

    A composite of the following variables to assess perinatal healthcare engagement: 1) Attended at least ~75% of the recommended prenatal visits; 2) Attended postpartum visit; 3) Received recommended vaccination during pregnancy.

Secondary outcomes

  1. Trust in Provider

    Time frame: Baseline; third trimester, and postpartum

    A validated 11-item instrument used to measure patients' trust in the provider regarding dependability, confidence, and confidentiality of information.

  2. Reported Discrimination

    Time frame: Baseline, third trimester and postpartum

    Measured with a validated survey of patient self-report on how often in the past 12 months, individuals felt treated poorly due to race.

  3. Perceived Stress

    Time frame: Baseline, third trimester and postpartum

    Measured with Cohen's Perceived Stress Scale

  4. Depression

    Time frame: Baseline, third trimester and postpartum

    Measured with the Patient Health Questionnaire-9 (PHQ-9)

  5. Cesarean birth

    Time frame: At study completion

    Cesarean birth for any indication other than prior cesarean

  6. Unplanned healthcare utilization

    Time frame: Up to 12 months postpartum

    Prenatal or postpartum (up to 12 weeks postpartum) unplanned emergency room visits or hospitalizations.

  7. Severe Maternal Morbidity

    Time frame: Up to 12 months postpartum

    Composite outcome of the following diagnoses using ICD-10 codes: acute myocardial infarction, aneurysm, acute renal failure, adult respiratory distress syndrome, amniotic fluid embolism, cardiac arrest, disseminated intravascular coagulation, eclampsia, heart failure, puerperal cerebrovascular disorders, pulmonary edema, severe anesthesia complications, sepsis, shock, sickle cell disease with crisis, air and thrombotic embolism blood products transfusion, hysterectomy, temporary tracheostomy, ventilation.

  8. Breastfeeding Initiation

    Time frame: Up to 12 months postpartum

    Rates of breastfeeding initiation prior to discharge from the hospital

  9. Group-Based Medical Mistrust Scale

    Time frame: Baseline; Week 27 up to birth (third trimester); Birth up to Week 40 (Postpartum)

    A 12-item validated survey focused on healthcare provided in the social context of racism and discrimination.

Study contacts

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

Anna Palatnik, MD

CONTACT

[email protected]

(414) 805-6624

Joni S Williams, MD, MPH

CONTACT

[email protected]

(414) 955-8827

Sponsors and collaborators

Lead sponsor

Medical College of Wisconsin

Other

Registry information

Acronym: BUNDLE

Important dates

Study start
2025
Primary completion
2029
Study completion
2030
First posted
Aug 15, 2023
Registry last updated
Jul 20, 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.

Published trials that share one or more normalized conditions with this study.