- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01925664
Doula Support for Young Mothers: A Randomized Trial
Study Overview
Status
Conditions
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
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Illinois
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Chicago, Illinois, United States, 60637
- University of Chicago
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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.
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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.
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No Intervention: Usual Care
Mothers received normal prenatal and obstetric clinical care and had access to social work case management.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Breastfeeding Initiation
Time Frame: Three days postpartum
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Three days postpartum
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Positive parenting behavior (Parent Child Observation Guide)
Time Frame: 4 months postpartum
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Videotaped interactions between mothers and infants coded by masked observers
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4 months postpartum
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Breastfeeding duration
Time Frame: 4- and 12 months postpartum
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4- and 12 months postpartum
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Positive parenting behaviors (Parent Child Observation Guide)
Time Frame: 12- and 24 months postpartum
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Videotaped interactions between mothers and infants coded by masked observers
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12- and 24 months postpartum
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Use of labor anesthesia
Time Frame: Start of labor through childbirth
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Start of labor through childbirth
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Labour Agentry Scale
Time Frame: 1 day postpartum
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The Labour Agentry Scale is a self-report scale that assesses maternal feelings of efficacy during labor
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1 day postpartum
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Adult Adolescent Parenting Inventory (AAPI)
Time Frame: 4 months postpartum
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The AAPI is a self report scale that measures appropriate parenting attitudes
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4 months postpartum
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Maternal Self-Efficacy Scale
Time Frame: 4-, 12-, and 24 months postpartum
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The Maternal Self-Efficacy Scale is a self report scale that measures parenting efficacy with regard to infant care.
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4-, 12-, and 24 months postpartum
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Parenting Stress Index (PSI)
Time Frame: 4-, 12-, and 24 months postpartum
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The PSI is a self report scale that measures parenting stress and parent perceptions of the difficulty of her child
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4-, 12-, and 24 months postpartum
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Center for Epidemiologic Studies Depression Scale (CES-D)
Time Frame: 4-, 12-, and 24 months postpartum
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The CES-D is a self report scale that measures depressive symptoms experienced in the prior week.
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4-, 12-, and 24 months postpartum
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Timing of solid food introduction to infant
Time Frame: 4- and 12 months postpartum
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4- and 12 months postpartum
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The Brief Infant Toddler Social Emotional Assessment (BITSEA)
Time Frame: 12- and 24 months postpartum
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The BITSEA is a parent report measure that assesses problem behaviors and social competence in infants and toddlers.
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12- and 24 months postpartum
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Mullen Scales of Early Learning
Time Frame: 24 months postpartum
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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.
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24 months postpartum
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Sydney L Hans, PhD, University of Chicago
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- R40 MC 00203
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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