NCT01338727已完成不适用
Breastfeeding Education and Support Trial for Obese Women (BESTOW)
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 206
- 试验地点
- 2
- 主要终点
- Exclusive Breastfeeding Rate
研究概览
简要总结
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Health Services Research
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •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
排除标准
- •HIV positive or having other conditions which interfere with exclusive breastfeeding
- •Infant admitted to the Neonatal Intensive Care Unit
结局指标
主要结局
Exclusive Breastfeeding Rate
时间窗: 3 months postpartum
次要结局
- Breastfeeding Rate(3 months postpartum)
- Breastfeeding Initiation Rate(For the duration of the hospital stay, average equals 3 days)
研究者
研究点 (2)
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