Is a
Clinical Study attributes
NCT Number
Trial Recruitment Size
2060
Trial Sponsor
Clinical Trial Start Date
2006
0Primary Completion Date
2010
0Study Completion Date
2010
0Clinical Trial Study Type
Interventional0
Interventional Trial Purpose
Health Services Research0
Intervention Type
Behavioral0
Interventional Trial Phase
Not Applicable0
Participating Facility
Official Name
Breastfeeding Education and Support Trial for Obese Women (BESTOW)0
Last Updated
April 19, 2011
0Allocation Type
Randomized0
Intervention Model
Parallel Assignment0
Masking Type
None (Open Label)0
Other attributes
Intervention Treatment
Breastfeeding Peer Counseling0
Study 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.
Timeline
No Timeline data yet.
Further Resources
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