Doula Support for Young Mothers: A Randomized Trial

September 4, 2013 updated by: University of Chicago
The goal of this study was to evaluate the impact of a doula home visiting intervention on young, low-income mothers' birth outcomes, breastfeeding, postpartum depressive symptoms, and parenting, and on their children's development.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

The goal of this study is to evaluate a doula home visiting model -- sometimes called the "community doula model." This model differs from typical hospital based doula interventions in several ways. Doulas are providers from the same community backgrounds as their clients. Services are not just provided during labor and delivery, but throughout the final trimester and during the first weeks after delivery. Prenatal and postpartum services are provided in the homes of the mothers. The model was developed specifically for working with low-income mothers and with young mothers.

A two-armed randomized controlled trial was conducted at the University of Chicago Hospitals. Participants were recruited through two out-patient obstetric clinics affiliated with the Hospitals. The clinics primarily served a low-income, African-American population, reflective of the families in the communities near to the hospital. The study was open to all young women receiving prenatal care at the clinics who met age and eligibility criteria. After providing informed consent and completing a baseline interview, participants were randomized into two groups. The experimental group, in addition to receiving regular clinical care, received weekly home visiting services from a doula and the support of a doula at the hospital during labor and delivery. Doulas worked with their clients until three months postpartum. The control group received standard clinical care and had access to social work case management.

Four paraprofessional doulas delivered the study intervention. Before providing study services, doulas had been trained to provide childbirth education, labor support, breastfeeding education, and parent-child interaction support.

Followup research assessments of the doula and control group mothers and infants were conducted during the first three days postpartum, at 4 months postpartum, at 12 months postpartum, and at 24 months postpartum. 80% of the sample was retained through the 24 month followup assessment. Follow up assessments involved interviews with the mothers, videotaping of mother-infant interaction, and behavioral assessment of the infants. Obstetric and newborn hospital medical charts were also reviewed.

The study evaluated outcomes that have been the focus of prior studies of hospital-only doula services: use of obstetrical intervention in labor and delivery (anesthesia, surgical delivery), mother labor efficacy, breastfeeding, and maternal depression. A major contribution of this study is to explore longer term outcomes not evaluated in prior studies of doula intervention, particularly parenting and child development outcomes. The study evaluated multiple dimensions of parenting including parenting behavior (sensitivity, stimulation), parenting efficacy, parenting attitudes, and parenting stress. Child development outcomes included cognitive development and early behavior problems.

Study Type

Interventional

Enrollment (Actual)

248

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Illinois
      • Chicago, Illinois, United States, 60637
        • University of Chicago

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

12 years to 19 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • pregnant and less than 34 weeks gestation
  • planning to deliver at study hospital
  • between ages 14 and 21

Exclusion Criteria:

  • planning to move out of community after giving birth
  • planning to give up custody of infant
  • prior c-section delivery

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Doula
Mothers received doula home visiting services in addition to normal prenatal and obstetric clinical care and had access to social work case management.
This intervention included doulas providing weekly home visits during the last trimester of pregnancy and up to three months postpartum. Home visits focused on prenatal health, preparation for childbirth, breastfeeding education, and developing a relationship with the baby. Doulas also were present in the hospital during labor, delivery, and postpartum providing emotional support, non-medical comfort measures, and breastfeeding counseling.
No Intervention: Usual Care
Mothers received normal prenatal and obstetric clinical care and had access to social work case management.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Breastfeeding Initiation
Time Frame: Three days postpartum
Three days postpartum
Positive parenting behavior (Parent Child Observation Guide)
Time Frame: 4 months postpartum
Videotaped interactions between mothers and infants coded by masked observers
4 months postpartum

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Breastfeeding duration
Time Frame: 4- and 12 months postpartum
4- and 12 months postpartum
Positive parenting behaviors (Parent Child Observation Guide)
Time Frame: 12- and 24 months postpartum
Videotaped interactions between mothers and infants coded by masked observers
12- and 24 months postpartum
Use of labor anesthesia
Time Frame: Start of labor through childbirth
Start of labor through childbirth
Labour Agentry Scale
Time Frame: 1 day postpartum
The Labour Agentry Scale is a self-report scale that assesses maternal feelings of efficacy during labor
1 day postpartum
Adult Adolescent Parenting Inventory (AAPI)
Time Frame: 4 months postpartum
The AAPI is a self report scale that measures appropriate parenting attitudes
4 months postpartum
Maternal Self-Efficacy Scale
Time Frame: 4-, 12-, and 24 months postpartum
The Maternal Self-Efficacy Scale is a self report scale that measures parenting efficacy with regard to infant care.
4-, 12-, and 24 months postpartum
Parenting Stress Index (PSI)
Time Frame: 4-, 12-, and 24 months postpartum
The PSI is a self report scale that measures parenting stress and parent perceptions of the difficulty of her child
4-, 12-, and 24 months postpartum
Center for Epidemiologic Studies Depression Scale (CES-D)
Time Frame: 4-, 12-, and 24 months postpartum
The CES-D is a self report scale that measures depressive symptoms experienced in the prior week.
4-, 12-, and 24 months postpartum
Timing of solid food introduction to infant
Time Frame: 4- and 12 months postpartum
4- and 12 months postpartum
The Brief Infant Toddler Social Emotional Assessment (BITSEA)
Time Frame: 12- and 24 months postpartum
The BITSEA is a parent report measure that assesses problem behaviors and social competence in infants and toddlers.
12- and 24 months postpartum
Mullen Scales of Early Learning
Time Frame: 24 months postpartum
The Mullen is an assessment tool that measures child motor, cognitive, and language development. Trained assessors administered the instrument to the toddlers of study mothers.
24 months postpartum

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Sydney L Hans, PhD, University of Chicago

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2001

Primary Completion (Actual)

August 1, 2006

Study Completion (Actual)

August 1, 2006

Study Registration Dates

First Submitted

August 14, 2013

First Submitted That Met QC Criteria

August 16, 2013

First Posted (Estimate)

August 20, 2013

Study Record Updates

Last Update Posted (Estimate)

September 5, 2013

Last Update Submitted That Met QC Criteria

September 4, 2013

Last Verified

September 1, 2013

More Information

Terms related to this study

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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