Actively Recruiting

Phase Not Applicable
Age: 15Years - 49Years
FEMALE
Healthy Volunteers
ID05365815

Black Midwives for Black Women: Maternity Care to Improve Trust and Attenuate Structural Racism

Led by University of Illinois at Chicago · Updated on 2024-07-03

432

Participants Needed

1

Research Sites

37 weeks

Total Duration

On this page

Sponsors

U

University of Illinois at Chicago

Lead Sponsor

P

Patient-Centered Outcomes Research Institute

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating if a group-based maternity care approach can improve trust and engagement among Black pregnant individuals. This study compares Melanated Group Midwifery Care (MGMC), a culturally focused group prenatal care program led by Black midwives and supported by Black care coordinators and postpartum doulas, with usual individualized obstetric care. The trial aims to address structural racism in maternity care and enhance patient experiences for Black birthing people. Participants will be randomly assigned to either MGMC or usual care. In MGMC, groups of 8-12 Black pregnant women meet regularly with the same Black midwife and care coordinator for prenatal and one postnatal visit. A care coordinator supports patients proactively throughout pregnancy and up to one year postpartum. Postpartum doulas provide support through home visits and ongoing contact for the first year after birth. The usual care group receives standard individual prenatal visits with midwives or obstetricians without guaranteed continuity or racial concordance. All participants will complete surveys measuring patient trust, respect, engagement, and mental wellbeing at six time points: three during pregnancy and three up to 12 months postpartum. Additional interviews will explore experiences of medically and socially complex patients. Researchers will monitor how MGMC integrates into practice and assess patient engagement and satisfaction outcomes. The study will continue until February 2027, involving ongoing follow-up and data collection throughout pregnancy and postpartum periods.

CONDITIONS

Brief Title

Melanated Group Midwifery Care (MGMC)

Who Can Participate

Age: 15Years - 49Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Pregnant women who self-identify as Black on a standard prenatal intake form
  • Less than 20 weeks pregnant
  • 15 years old or older
  • Present to the general obstetrics group at the University of Chicago Medical Center for their new prenatal visit
  • Speak and understand English
  • All Black midwives, care coordinators, and community postpartum doulas at the University of Chicago are eligible to participate
Not Eligible

You will not qualify if you...

  • Having a condition requiring care at a higher level of obstetrics (e.g., maternal fetal medicine) for the new prenatal visit
  • Having a cognitive issue that impairs the ability to give informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - From enrollment until birth (approximately up to 40 weeks of pregnancy)

Participants receive prenatal care through either Melanated Group Midwifery Care with group visits and coordinated support or usual individualized obstetric care.

Prenatal visits in groups approximately every few weeks with the same midwife and care coordinator; usual care participants attend individually scheduled prenatal visits

Outpatient Treatment

Duration - Up to 12 months postpartum

For participants in the Melanated Group Midwifery Care group, postpartum support is provided by a trained postpartum doula with home visits and ongoing contact. All participants complete postpartum assessments.

Postpartum home visits and contacts by doula for MGMC participants; postpartum assessments at 2, 6, and 12 months for all participants

Trial Site Locations

Total: 1 location

1

University of Illinois at Chicago

Chicago, Illinois, United States, 60612-7316

Actively Recruiting

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Research Team

K

Kylea L Liese, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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