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临床试验/NL-OMON20682
NL-OMON20682招募中不适用

Improving Care of Pregnant Women in the Netherlands by early identification of Perinatal & Maternal Risks. Pregnancy Risk Flagging System Phase 2: satisfaction

Philips Experience Design0 个研究点目标入组 164 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
164

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Pregnant women with a viable and non-anomalous foetus at the 20 weeks anomaly scan
  • 18 years or older
  • Able to read and understand English and/or Dutch language (we are aware this could lead to selection bias but in this phase of the experiment, questionnaires will only be available in English and Dutch)
  • Have smartphone and internet access
  • iPhone: at least iPhone 7, running the latest iOS version that is on the market at the date of starting the study
  • Android: not older than 5 years old phone running at least Android 6.0
  • Willing and able to provide informed consent (IC)

排除标准

  • Anomalous foetus at the 20 weeks ultrasound
  • In case the pregnant woman continues her ANC visits before 35-37 weeks of gestation in another hospital other than Máxima MC or another midwifery practice other than PUUR or 040 Verloskunde (because HCPs at other centres do not have access to the PRFS dashboard prototype, and the pregnant women did not receive the PCQ and SUS questionnaires at that time yet)
  • Delivery before the second questionnaire measurement at 35-37 weeks of gestation
  • Perinatal death

研究者

发起方
Philips Experience Design

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