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临床试验/NL-OMON46134
NL-OMON46134已完成不适用

Cognitive Bias Modification: Exploring the effects of a computer-based cognitive bias training in patients with acute myeloid leukemia at risk for depression and anxiety symptoms -(HemaCogTrain) - Cognitive bias modification in leukaemia patients

Radboud Universitair Medisch Centrum0 个研究点目标入组 20 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
20

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

年龄范围
18 至 64(—)

入选标准

  • - Subjected to the ward of the department of hematology-oncology for treatment of a AML
  • - Hightened level of distress as measured with the *Distress Thermometer*. A *Distress Thermometer* score of 5 or higher was originally recommended as denoting significant distress necessitating psychosocial referral (National Comprehensive Cancer Network, 2005). Patients with a score of 8 or higher in the HADS will be considered for participation in the study. (HADS; Zigmond & Snaith, 1983). This cut-off shows good sensitivity and specificity in a somatic patient population (Bjelland et al., 2002).
  • - Signed IRB-approved informed consent form

排除标准

  • - Impossibility to obtain a valid informed consent
  • - Severe depression or other psychiatric disorders that interfere with the ability to receive a cognitive intervention of 20 minutes per day
  • - Insufficient comprehension of the Dutch language
  • - IQ estimate < 80 points
  • - Acuteness of symptoms that prevent patient from attentively doing the task 20 min

研究者

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