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N/A N=30 Randomized Supportive Care

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

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

Enrolled (actual)
30
Serious AEs
0.0%
Results posted
Feb 2026
Primary outcome: Primary: Perceptions of Provider Communication — 1.42; 1.86 score on a scale

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Doula Care (Behavioral)
Age
Pediatric, Adult · 16+ yrs
Sex
Female
Sponsor
University of Kansas Medical Center
Primary completion
Nov 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Perceptions of Provider Communication
1.42; 1.86
PRIMARY
Perceptions of Maternal Care
4.50; 4.36
SECONDARY
Perinatal Outcome - Gestational Age (GA) at Delivery
37.5; 38.1
SECONDARY
Perinatal Outcome - Number of Participants With Preterm <37 Weeks Births
2; 1
SECONDARY
Perinatal Outcome - Number of Participants With Cesarean Sections
7; 9
SECONDARY
Perinatal Outcome - Number of Participants With Gestational Hypertension/Preeclampsia
5; 0
SECONDARY
Neonatal Morbidity
1; 1
SECONDARY
Neonatal Morbidity
1; 1
SECONDARY
Antepartum Depression
7.8; 10.4
SECONDARY
Postpartum Depression
7.7; 6.9
SECONDARY
Maternal Pain Management
25.00; 32.25
SECONDARY
Maternal Pain Management
25.00; 32.25
SECONDARY
Lactation Status - Number of Participants Lactating and Breastfeeding
10; 13
SECONDARY
Lactation Status - Number of Participants Lactating and Breastfeeding After L&D Discharge
7; 9

Summary

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

Eligibility Criteria

Inclusion Criteria

  • Black birthing people
  • Received care and plan to delivery at the University of Kansas Medical Center
  • Scored positive to social determinants of health screener
  • Gestational age between 14-27.6 weeks at enrollment

Exclusion Criteria

  • Pregnancy not viable or pregnancy not intrauterine on ultrasound
  • Patients who are not willing to be randomized into not receiving doula enhanced
  • Patients who do not plan to delivery at the University of Kansas Health System
  • Non-Black birthing people.
  • Planned cesarean section
  • Patients with a known major fetal anomaly
  • Non-English speaking
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT07157059). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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