跳至主要内容
临床试验/NL-OMON20793
NL-OMON20793尚未招募不适用

The (cost) effectiveness of an online intervention (MamaKits) for pregnant women with affective symptoms: a randomised controlled trial

VU medical center0 个研究点目标入组 286 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
286

研究概览

简要总结

/A

研究设计

研究类型
Interventional

入排标准

入选标准

  • participants of 18 years and older,
  • who are pregnant at any stage of pregnancy, but not later than 10 weeks before the expected delivery date,
  • Who have at least mild symptoms of depression and/or anxiety, defined by Center for Epidemiological Studies Depression scale (CES-D) higher than 16 and /or a score higher than 8 on the Hospital Anxiety and Depression scale (HADS-A)

排除标准

  • Participants who indicate that they either intend to harm themselves or to attempt suicide (as assessed by one question [210]) will be excluded and advised to consult their general practitioner to obtain more tailored care.

研究者

发起方
VU medical center

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