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临床试验/NCT01338727
NCT01338727已完成不适用

Breastfeeding Education and Support Trial for Obese Women (BESTOW)

University of Connecticut2 个研究点 分布在 1 个国家目标入组 206 人开始时间: 2006年9月最近更新:
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

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

申办方类型
Other

研究点 (2)

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