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Breastfeeding Education and Support Trial for Obese Women (BESTOW)

Not Applicable
Completed
Conditions
Exclusive Breastfeeding
Breastfeeding Initiation
Registration Number
NCT01338727
Lead Sponsor
University of Connecticut
Brief Summary

The primary objective of this study is to evaluate the efficacy of a specialized exclusive breastfeeding education and support program targeting obese, pregnant, low-income women in Hartford, CT. Specifically, the investigators will evaluate the impact of the intervention on exclusive and partial breastfeeding rates at birth, 1, 3 and 6 months pp. Secondary aims of this study are: a) to characterize postpartum weight loss patterns and blood pressure values of obese women, by study group; and b) to evaluate potential differences in infant morbidity (diarrhea, otitis media and rehospitalization), by study group.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
206
Inclusion Criteria
  • obese (prepregnant BMI 27.0 or greater)
  • pregnant women delivering at Hartford Hospital
  • no more than 34 weeks gestation
  • considering breastfeeding this child
  • low income (<185% Federal poverty level)
  • planning to remain in the greater Hartford area for 6 months postpartum
  • must have access to a telephone for follow-up interviews
  • delivery of a healthy, term, singleton
Exclusion Criteria
  • HIV positive or having other conditions which interfere with exclusive breastfeeding
  • Infant admitted to the Neonatal Intensive Care Unit

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Exclusive Breastfeeding Rate3 months postpartum
Secondary Outcome Measures
NameTimeMethod
Breastfeeding Rate3 months postpartum
Breastfeeding Initiation RateFor the duration of the hospital stay, average equals 3 days

Trial Locations

Locations (1)

University of Connecticut

🇺🇸

Storrs, Connecticut, United States

University of Connecticut
🇺🇸Storrs, Connecticut, United States

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