NCT05510284已完成不适用
Post-partum Care in the NICU
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 37
- 试验地点
- 2
- 主要终点
- Time to receipt of postpartum care
研究概览
简要总结
This is a pilot randomized control trial to demonstrate the feasibility of a novel model of dyad-centered, doula-coordinated, midwife-delivered postpartum care located in the NICU in a large urban hospital.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Preterm birth <34 weeks
- •Signed medical record release form
排除标准
- •Unable to read or sign informed consent
- •If the medical team believes that the infant may die or be transferred to another hospital in upcoming weeks
- •PI Discretion
结局指标
主要结局
Time to receipt of postpartum care
时间窗: birth until 6 weeks post-partum
To be analyzed using a wilcoxin rank sum test
次要结局
- Receipt of Postpartum care(birth until 6 weeks post-partum)
- Comparison of effectiveness of intervention for mothers with infants less than 29 weeks gestational age vs those 29 weeks or older.(birth until 6 weeks post-partum)
- Comparison of effectiveness of intervention for mothers with public vs private insurance(birth until 6 weeks post-partum)
研究者
Heather Burris
Associate Professor of Pediatrics
University of Pennsylvania
研究点 (2)
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