跳至主要内容
临床试验/NCT02185625
NCT02185625已完成不适用

Reduction of Adverse Pregnancy Outcomes With a Smartphone Application in Ghana: a Cluster Randomized Trial

University of Aarhus15 个研究点 分布在 1 个国家目标入组 3,773 人开始时间: 2014年7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
3,773
试验地点
15
主要终点
Postpartum Hemorrhage.

研究概览

简要总结

The purpose of this study is to determine whether use of the Safe Delivery smartphone application by midwives can reduce excess blood loss from bleeding, and infant death during childbirth in Ghanaian women. Moreover, it will be investigated whether the Safe Delivery application can increase midwives' knowledge and skills in managing childbirth.

Fifteen hospitals in Greater Accra, Ghana, will be cluster randomized to either use the Safe Delivery application (intervention), or to no intervention (control). In the intervention hospitals, midwives will be educated in the use of Safe Delivery. Pregnant women will be enrolled at delivery and followed until 7 days postpartum. Data collection will begin July 2014 and is expected to be finished by October 2014.

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

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Postpartum Hemorrhage.

时间窗: Measurements 2 hours after delivery.

Postpartum Hemorrhage is defined as blood loss greater than 500 ml from bleeding associated with childbirth within first 2 hours postpartum.

次要结局

  • Key feature questionnaire (KFQ).(At baseline and 2 months after randomization.)
  • Objective structured assessment of technical skill (OSATS).(At baseline and 2 months after randomization.)
  • Neonatal mortality 7 days postpartum.(Within 7 days postpartum.)
  • Blood loss(Measurements 2 hours after delivery.)
  • Fresh stillbirth(At delivery.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (15)

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