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A randomized comparative-effectiveness study of two enhanced prenatal care models for low-income pregnant people: Engaging Mothers & Babies; Reimagining Antenatal Care for Everyone (EMBRACE)

Improving perinatal mental health and care experiences and preventing adverse maternal and infant outcomes are essential prenatal care components, yet existing services often miss the mark, particularly for low-income populations. An enhanced group prenatal care program, “Glow! Group Prenatal Care a...

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Published in:Contemporary clinical trials 2024-08, Vol.143, p.107568, Article 107568
Main Authors: Kuppermann, Miriam, Pressman, Alice, Coleman-Phox, Kimberly, Afulani, Patience, Blebu, Bridgette, Carraway, Kristin, Butcher, Brittany Chambers, Curry, Venise, Downer, Chris, Edwards, Brittany, Felder, Jennifer N., Fontenot, Jazmin, Garza, Mary A., Karasek, Deborah, Lessard, Lauren, Martinez, Erica, McCulloch, Charles E., Oberholzer, Christy, Ramirez, Guadalupe R., Tesfalul, Martha, Wiemann, Andrea
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Language:English
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Summary:Improving perinatal mental health and care experiences and preventing adverse maternal and infant outcomes are essential prenatal care components, yet existing services often miss the mark, particularly for low-income populations. An enhanced group prenatal care program, “Glow! Group Prenatal Care and Support,” was developed in California's Central Valley in response to poor perinatal mental health, disrespectful care experiences, and high rates of adverse birth outcomes among families with low incomes. Engaging Mothers & Babies; Reimagining Antenatal Care for Everyone (EMBRACE) is a pragmatic, two-arm, randomized, comparative-effectiveness study designed to assess depression (primary outcome), the experience of care (secondary outcome), and preterm birth (exploratory outcome) among Medi-Cal (California's Medicaid program)-eligible pregnant and birthing people, comparing those assigned to Glow! Group Prenatal Care and Support (Glow/GC) with those assigned to enhanced, individual prenatal care through the California Department of Public Health's Comprehensive Perinatal Services Program (CPSP/IC). Participating clinical practices offer the two comparators, alternating between comparators every 6 weeks, with the starting comparator randomized at the practice level. Participant-reported outcomes are assessed through interviewer-administered surveys at study entry, during the participant's third trimester, and at 3 months postpartum; preterm birth and other clinical outcomes are abstracted from labor and delivery records. Patient care experiences are further assessed in qualitative interviews. The protocol complies with the Standard Protocol Items for Randomized Trials. This comparative-effectiveness study will be used to determine which of two forms of enhanced prenatal care is more effective, informing future decisions regarding their use. Trial Registration: ClinicalTrials.gov: NCT04154423.
ISSN:1551-7144
1559-2030
1559-2030
DOI:10.1016/j.cct.2024.107568