Chapman, D. J., Damio, G., Young, S., & Perez-Escamilla, R. (2004). Effectiveness of breastfeeding peer counseling in a low-income, predominantly Latina population: A randomized controlled trial. Archives of Pediatrics & Adolescent Medicine, 158(9), 897-902. https://doi.org/10.1001/archpedi.158.9.897
Screening decision | Screening conclusion | HomVEE procedures and standards version |
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Passes screens | Eligible for review | Version 2 |
Rating | Design | Attrition | Baseline equivalence | Compromised randomization | Confounding factors | Valid, reliable measure(s) |
---|---|---|---|---|---|---|
High | Randomized controlled trial | Low | Not assessed for randomized controlled trials with low attrition |
No | No |
Yes |
Study participants | Pregnant women were recruited at prenatal clinics. To be eligible, the mother had to be age 18 or older, up to 26 weeks pregnant, and have low income (that is, participating in the Supplemental Nutrition Program for Women, Infants, and Children or in the Supplemental Nutrition Assistance Program, or with a household income below 180 percent of the federal poverty level). At the time of birth, mother-child dyads were screened a final time and eligible for the study if the newborn was born healthy at full term, had no congenital anomalies and no maternal history of human immunodeficiency virus, and was not admitted to the neonatal intensive care unit. Among eligible mothers, 90 were randomly assigned to the Breastfeeding: Heritage and Pride™ (BHP) home visiting group and 75 to the comparison group. Outcomes were measured at birth and at one month, three months, and six months postpartum. Eighty percent of mothers were Hispanic, nine percent were African American, four percent were White, and eight percent reported they were another race. |
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Setting | The study took place in Hartford, Connecticut. |
Intervention services | The Breastfeeding: Heritage and Pride™ (BHP) intervention consisted of at least one prenatal home visit, daily in-hospital visits during postpartum hospitalization, and three postpartum home visits. These visits were conducted by peer counselors, one of whom was assigned to each mother-child dyad. During the prenatal home visit, the peer counselor provided education on a range of topics including the benefits of breastfeeding, common breastfeeding myths, behaviors that impede early initiation and successful breastfeeding, infant feeding cues, and proper latch-on technique or positioning. During the postpartum period, mothers received the first home visit within 24 hours of discharge from the hospital. The peer counselor provided one-on-one breastfeeding support and counseling based on the mother’s needs. Free mini-electric breast pumps were provided to mothers who needed one. |
Comparison conditions | Mothers assigned to the comparison group received routine breastfeeding education. This included written materials on breastfeeding and individualized breastfeeding information in response to questions at prenatal visits. During postpartum hospitalization, mothers received one-on-one assistance and education from staff nurses, and had access to a certified lactation consultant for serious breastfeeding problems. During the postpartum period, mothers could also call the hospital to speak with a registered nurse who could answer questions about breastfeeding. |
Subgroups examined |
This field lists subgroups examined in the manuscript (even if they were not replicated in other samples and not reported on the summary page for this model’s report). There were no subgroups reported in this manuscript. |
Funding sources | This research was supported by the Centers for Disease Control and Prevention through a subcontract with the Association of Teachers of Preventative Medicine; Connecticut Family Nutrition Program for Infants, Toddlers, and Children; and the Hartford Hospital Research Foundation. |
Author affiliation | The authors are affiliated with the University of Connecticut, the Hispanic Health Council, and Hartford Hospital. One of the authors is affiliated with the Hispanic Health Council, which sponsors the Breastfeeding: Heritage and Pride™ home visiting model. |
Peer reviewed | Yes |
Clinicaltrials.gov Identifier: None found. SocialScienceRegistry.org Identifier: None found. Registry of Efficacy and Effectiveness Studies Identifier: None found. Study registration was assessed by HomVEE for Clinicaltrials.gov beginning with the 2014 review, and for other registries beginning with the 2021 review.
Findings that rate moderate or high
Rating | Outcome measure | Effect | Sample | Timing of follow-up | Sample size | Intervention group | Comparison group | Group difference | Effect size | Statistical significance | Notes |
---|---|---|---|---|---|---|---|---|---|---|---|
High | Exclusive breastfeeding |
FavorableUnfavorable or ambiguousNo Effect |
BHP and conventional breastfeeding support vs. conventional breastfeeding support RCT, Connecticut, 2000-2003, full sample |
1 month old |
157 mother/child dyads | Not reported | Not reported | Not reported | Study reported = 1.07 | Not statistically significant, p ≥ 0.05 |
Negative effect is favorable to the intervention. The reported effect size is the relative risk, which is expressed as a positive value. |
High | No initiation or cessation of breastfeeding |
FavorableUnfavorable or ambiguousNo Effect |
BHP and conventional breastfeeding support vs. conventional breastfeeding support RCT, Connecticut, 2000-2003, full sample |
3 months old |
153 mother/child dyads | Unadjusted proportion = 0.56 | Unadjusted proportion = 0.71 | Mean difference = -0.15 | Study reported = 0.78 | Not statistically significant, p ≥ 0.05 |
Negative effect is favorable to the intervention. The reported effect size is the relative risk, which is expressed as a positive value. |
High | No initiation or cessation of breastfeeding |
FavorableUnfavorable or ambiguousNo Effect |
BHP and conventional breastfeeding support vs. conventional breastfeeding support RCT, Connecticut, 2000-2003, full sample |
6 months old |
144 mother/child dyads | Not reported | Not reported | Not reported | Study reported = 0.94 | Not statistically significant, p ≥ 0.05 |
Negative effect is favorable to the intervention. The reported effect size is the relative risk, which is expressed as a positive value. |
High | No initiation or cessation of breastfeeding |
FavorableUnfavorable or ambiguousNo Effect |
BHP and conventional breastfeeding support vs. conventional breastfeeding support RCT, Connecticut, 2000-2003, full sample |
birth |
165 mother/child dyads | Unadjusted proportion = 0.09 | Unadjusted proportion = 0.23 | Mean difference = -0.14 | Study reported = 0.39 | Statistically significant, p <0.05 |
Negative effect is favorable to the intervention. The reported effect size is the relative risk, which is expressed as a positive value. |
High | No initiation or cessation of breastfeeding |
FavorableUnfavorable or ambiguousNo Effect |
BHP and conventional breastfeeding support vs. conventional breastfeeding support RCT, Connecticut, 2000-2003, full sample |
1 month old |
157 mother/child dyads | Unadjusted proportion = 0.36 | Unadjusted proportion = 0.49 | Mean difference = -0.14 | Study reported = 0.72 | Not statistically significant, p ≥ 0.05 |
Negative effect is favorable to the intervention. The reported effect size is the relative risk, which is expressed as a positive value. |