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N/A N=168 Randomized Single-blind Treatment

BOOST: Breastfeeding Onset and Onward With Support Tools

Breastfeeding Duration

Enrolled (actual)
168
Serious AEs
3.0%
Results posted
Jan 2025
Primary outcome: Primary: Number of Participants Breastfeeding Their Infants at 1 Month — 76; 74 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
WIC support + home-based individual support + Breastfeeding Incentives (SC+BFI) (Behavioral); WIC support + home-based individual support (SC) (Behavioral)
Age
Adult · 18+ yrs
Sex
Female
Sponsor
RTI International
Primary completion
Apr 2023

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants Breastfeeding Their Infants at 1 Month
76; 74
PRIMARY
Number of Participants Breastfeeding Their Infants at 3 Months
59; 53
PRIMARY
Number of Participants Breastfeeding Their Infants at 6 Months
46; 33
PRIMARY
Number of Participants Breastfeeding Their Infants at 9 Months
26; 19
PRIMARY
Number of Participants Breastfeeding Their Infants at 12 Months
21; 15
SECONDARY
Infant Weight
4090; 4241
SECONDARY
Infant Weight
4090; 4241
SECONDARY
Infant Weight
4090; 4241
SECONDARY
Infant Weight
4090; 4241
SECONDARY
Infant Weight
4090; 4241

Summary

This behavioral intervention trial will test whether a standard care breastfeeding intervention from the Special Supplemental Nutrition Program for Women, Infants, and Children (WIC) program plus monthly financial incentives contingent on observed breastfeeding will improve breastfeeding duration among low-income mothers compared to a standard (WIC) care control. Investigators hypothesize that the standard care plus monthly contingent financial incentives intervention will promote longer breastfeeding duration, fewer infant health issues, and greater healthcare cost savings than the standard care (control) intervention.

Eligibility Criteria

Inclusion Criteria

  • mothers must initiate breastfeeding
  • mothers must be WIC-enrolled or eligible to enroll in WIC services
  • mothers must reside and plan to stay in the study county for 12 months postpartum
  • mothers must consent voluntarily
  • mothers must understand fifth grade level of English
  • mothers must be at least 18 years old

Exclusion Criteria

  • mothers whose babies are medically contraindicated against breastfeeding
  • mothers who are hospitalized for severe postpartum medical issues
  • mothers who have ongoing illicit drug use issues
  • mothers who had a psychiatric hospitalization within the last three months
  • mothers who currently have suicidal thoughts or attempts
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03964454). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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