Labor Pain Clinical Trial
— BBBOfficial title:
Birth Sisters Best Beginnings Evaluation
NCT number | NCT02550730 |
Other study ID # | H-33788 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | August 2015 |
Est. completion date | June 2018 |
Verified date | July 2018 |
Source | Boston Medical Center |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Peer support during labor, birth and the perinatal period (also known as "doula" support) has been shown in some studies to reduce cesarean rates, postpartum depression and increase breastfeeding rates. The purpose of this program evaluation is to prospectively assess the clinical and cost outcomes of Boston Medical Center's Birth Sister doula program, one of the few established, hospital-based programs in the United States. To enhance the capability of the Birth Sisters Program to impact social determinants of perinatal health in a low-income population, the program evaluation will include the addition of Medical Legal Partnership for Children's (MLP) training and referral services. This program will be described as the Birth Sisters Best Beginnings services (BBB). The evaluation will compare the effects of BBB compared with no Birth Sister support for women receiving maternity care at Boston Medical Center. Eligible women will be randomly assigned either BBB services or usual care. All women will be consented and interviewed in the mid-second trimester of pregnancy and interviewed again at 6-8 weeks postpartum. Women randomized to the BBB will be offered 8 prenatal Birth Sister visits in the home or at Boston Medical Center starting at 6 months of pregnancy, continuous support through labor and birth, and up to 4 postpartum Birth Sister visits in the home or at Boston Medical Center. The usual care group will receive no birth sister support but does have access to standard interdisciplinary maternity care services. The primary outcomes will be reduction in cesarean rate. Secondary outcomes will include cost, labor interventions, infant outcomes, satisfaction with care and psychosocial outcomes, including depression, social functioning and self-efficacy.
Status | Completed |
Enrollment | 411 |
Est. completion date | June 2018 |
Est. primary completion date | May 2018 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 64 Years |
Eligibility |
Inclusion criteria: - Being a pregnant Woman 16 to 24 gestational age - First Time Mother - Singleton - Public insurance - No known fetal anomaly Exclusion criteria - < 18 years of age - high risk pregnancy defined by care in the high-risk prenatal clinic |
Country | Name | City | State |
---|---|---|---|
United States | Boston Medical Center | Boston | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Boston Medical Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Low birth weight, | total births<2500g/total births as assessed by medical record abstraction | at delivery | |
Other | Rates of breastfeeding initiation | Number of mothers initiating breastfeeding/total # mothers by medical record abstraction | 8 weeks postpartum | |
Other | Reductions in depressive symptoms | Number of mothers with depression scale scores>9/total # mothers | 8 weeks postpartum | |
Other | Lower health care costs than incremental program costs | medical center costs reported through hospital accounting system | 8 weeks postpartum | |
Other | Rates of breastfeeding continuation | percent of participants breastfeeding at 8 weeks postpartum by interview | 8 weeks postpartum | |
Other | Rates of breastfeeding exclusivity | percent of participants exclusively breastfeeding at 8 weeks pp by interview | 8 weeks postpartum | |
Primary | Rates of cesarean sections | total cesareans/total births as assessed by medical record abstraction | at delivery | |
Secondary | Rates of preterm birth | total preterm births/total births as assessed by medical record abstraction | at delivery |
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