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临床试验/NCT01945931
NCT01945931已完成不适用

Evaluation of a Smartphone Application to Reduce Adverse Pregnancy Outcomes in Ethiopia: A Cluster-randomised Controlled Trial

University of Copenhagen2 个研究点 分布在 1 个国家目标入组 3,601 人开始时间: 2013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
3,601
试验地点
2
主要终点
Perinatal mortality (stillbirth and early neonatal death)

研究概览

简要总结

The purpose of this trial is to determine if the safe delivery smartphone application distributed to health workers in Ethiopia will decrease perinatal mortality and the incidence of postpartum haemorrhage. It is also the purpose to determine if the safe delivery smartphone application distributed to health workers in Ethiopia will increase health workers knowledge and skills in intra-partum management of active management of third stage labour 2) treatment of post-partum haemorrhage 3) manual removal of placenta and 4) neonatal resuscitation.

详细描述

Abstract Hypothesis A safe delivery smartphone application distributed to health workers in Ethiopia will decrease perinatal mortality and the incidence of postpartum haemorrhage

A safe delivery smartphone application distributed to health workers in Ethiopia will increase health workers knowledge and skills in intra-partum management of active management of third stage labour 2) treatment of post-partum haemorrhage 3) manual removal of placenta and 4) neonatal resuscitation

Intervention A safe delivery smartphone application with animated videos to improve clinical management during delivery will be introduced in the intervention clusters

Design Cluster randomized controlled trial with health facilities as the unit of randomization

Area Nole Kaba, Haru, Homa, Genji and Gimbie districts in Ethiopia

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
10 Years 至 45 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

  • Women in active labor

排除标准

  • 未提供

结局指标

主要结局

Perinatal mortality (stillbirth and early neonatal death)

时间窗: Participants will be followed from delivery until 7 days postpartum

Postpartum haemorrhage

时间窗: Participants will be followed from delivery until two hours postpartum

次要结局

  • Health workers clinical performance in active management of third stage of labour, postpartum haemorrhage and manual removal of placenta(0, 6 and 12 months)
  • Health workers clinical performance in management of neonatal resuscitation(0, 6 and 12 months)
  • Health workers knowledge of management of active management of third stage of labour, manual removal of placenta and postpartum haemorrhage(0, 6 and 12 months)
  • Health workers knowledge of management of neonatal resuscitation(0, 6 and 12 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Stine Lund, MD, PhD fellow

MD, PhD fellow

University of Copenhagen

研究点 (2)

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