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Labor and Delivery Doula Program to Reduce Perinatal Morbidity and Mortality in Kansas

NCT07157059 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2026-02-19

Study results available
· View outcomes & findings →

Summary

The study was done to learn how doula-enhanced care provided to Black birthing people improved perceived communication and quality care.

Conditions

  • Pregnancy Related
  • Doula Care
  • Black Maternal and Infant Health
  • Prenatal Care

Interventions

BEHAVIORAL

Doula Care

Participants assigned to the Doula care group received care from the doula pre, during, and post delivery.

Sponsors & Collaborators

  • BioNexus KC

    collaborator UNKNOWN

  • Blue KC (Blue Cross Blue Shield)

    collaborator UNKNOWN

  • University of Kansas Medical Center

    lead OTHER

Principal Investigators

  • Angela Martin, MD · University of Kansas Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
16 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-05-12
Primary Completion
2024-11-01
Completion
2024-11-01

Countries

  • United States

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07157059 on ClinicalTrials.gov