- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00502697
Tennessee Connections for Better Birth Outcomes (BBO)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Preterm births (PTBs) are the leading cause of death in infants under the age of one. Tennessee (TN) is one of the lowest ranking states in the US for rates of PTBs (46th) and infant mortality (48th). Costs for neonatal care increase exponentially with decreasing gestational age, and there are lifelong consequences for families and communities. Despite medications and improved diagnostic tools, a 27% increase in PTBs has occurred in the past 20 years. With a history of one PTB, the probability of another PTB is approximately 30%. The risk of having another PTB rises to almost 70% if the woman has a history of more than one PTB. Relationships between a variety of factors (e.g., African American race, smoking, short interval between pregnancies, socio-environmental stressors) likely contribute to TN's high rate of PTBs. Several interventions have been identified to reduce PTBs and improve maternal and infant health indicators but with varying success; administering intramuscular injections of progesterone between 16 and 36 weeks gestation, providing some prenatal care in the home of women with a high risk pregnancy, increasing the interval between pregnancies, and reducing social factors that negatively impact health, such as smoking, substance abuse and stress.
The overall purpose of this study was to determine if a combined medical and biobehavioral intervention would prevent PTBs and reduce healthcare costs in a sample of women who have had a prior PTB. The medical intervention was conventional prenatal and postpartum clinic care. The biobehavioral intervention included certified nurse midwife home visitors who engaged women in an integrated System of Care (SOC) during their prenatal care. Care continued during the first 18 months of the infant's life by maternal-child nurse visitors. Home visits were in addition to regularly scheduled conventional prenatal and postpartum clinic care. Main study questions were:
Is there a difference in: 1) the length of gestational age of infants of high-risk pregnant women who receive the medical intervention and high-risk pregnant women who receive the SOC? 2) in health care costs between women who receive the medical intervention and the SOC? 3) intervals between the current pregnancy and a subsequent pregnancy across groups? and 4) in length of gestational age of current infant with gestational age of index prior preterm birth?
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Tennessee
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Nashville, Tennessee, United States, 37232
- Vanderbilt University Medical Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Documented history of previous preterm delivery. Defined as delivery from 20 weeks to 36 weeks 6 days gestation.
- Proven pregnancy
- Reside in Davidson County, Tennessee (TN) or surrounding county in 90 mile driving radius.
- Less than 24 weeks gestation at enrollment
- Will receive prenatal care at a Vnderbilt University Medical Center (VUMC) clinic
- Willing to accept nurse home visits and be randomly assigned to conventional care or care with home visits
- Speaks and understands English
- Between the ages of 18 and 40 years.
Exclusion Criteria:
- Known fetal anomaly that can not be managed conservatively or fetal demise
Maternal medical or obstetrical complications including:
- Current or scheduled cervical cerclage
- PROM in current pregnancy prior to enrollment
- Participation in an antenatal study in which the clinical status or intervention may influence gestational age at delivery
- Profound mental dysfunction or under guardianship
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Targeted Nurse Home Visits
Advanced practice nurses provide targeted behavioral interventions during home visits.
These visits were in addition to regularly scheduled conventional prenatal and postpartum clinic visits.
Specific protocols guided nurse interventions related to tobacco use, substance use and misuse, stress management, dental health, maternal infections, perinatal depressive symptoms, family violence, reproductive life plans and continuity of care.
Home visits were continued in the postpartum period (through 18 months post-delivery) with a continued focus on risk factors identified during the prenatal period and internatal health care.
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Advanced practice nurses provide targeted behavioral interventions during home visits.
These visits were in addition to regularly scheduled conventional prenatal and postpartum clinic care.
Specific protocols guided nurse interventions related to tobacco use, substance use and misuse, stress management, dental health, maternal infections, perinatal depressive symptoms, family violence, reproductive life plans and continuity of care.
Home visits were continued in the postpartum period (through 18 months post-delivery) with a continued focus on risk factors identified during the prenatal period and internatal health care.
Women in this group received conventional prenatal care and postpartum clinic care.
Other Names:
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Other: Conventional prenatal/postpartum care
Women assigned to the control arm of the study received conventional prenatal and postpartum clinic care.
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Women in this group received conventional prenatal care and postpartum clinic care.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Infant Gestational Age
Time Frame: Time of delivery
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Infant gestational age was determined by the weeks and days gestation documented in the maternal delivery record.
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Time of delivery
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Maternal Length of Stay at Delivery
Time Frame: Hospital discharge point following delivery
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Number of maternal hospital days associated with delivery
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Hospital discharge point following delivery
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Melanie Lutenbacher, PhD, Vanderbilt University
- Principal Investigator: Patricia Temple, MD, MPH, Ohio State University and Vanderbilt University
Publications and helpful links
General Publications
- Lutenbacher M, Gabbe PT, Karp SM, Dietrich MS, Narrigan D, Carpenter L, Walsh W. Does additional prenatal care in the home improve birth outcomes for women with a prior preterm delivery? A randomized clinical trial. Matern Child Health J. 2014 Jul;18(5):1142-54. doi: 10.1007/s10995-013-1344-4.
- Karp SM, Howe-Heyman A, Dietrich MS, Lutenbacher M. Breastfeeding initiation in the context of a home intervention to promote better birth outcomes. Breastfeed Med. 2013 Aug;8(4):381-7. doi: 10.1089/bfm.2012.0151. Epub 2013 Mar 13.
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 (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 070684
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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