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临床试验/NL-OMON38590
NL-OMON38590已完成不适用

A pilot study of Study I: Distressing information, the Psychophysiological response and Recall. - PILOT-Study I: Distressing information, Psychophysiology and Recall.

Academisch Medisch Centrum0 个研究点目标入组 40 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
已完成
入组人数
40

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 至 99(—)

入选标准

  • In order to be eligible to participate in Group 1 of this pilot study, a subject must meet all of the following criteria:
  • - Informed consent;
  • - Having had cancer or being treated for cancer with a curative intent, with the exception of having (had) esophageal cancer.
  • - Diagnosed with cancer within a time span of 1 to 5 years ago;;Group 2
  • In order to be eligible to participate in Group 2 of this pilot study, a subject must meet all of the following criteria:
  • - Informed consent;
  • - *Healthy*, meaning:
  • * Never having had cancer
  • * Currently not visiting any medical specialist for another serious medical condition

排除标准

  • Subjects are not eligible if one or more of the following criteria apply:
  • - Those who suffer from cardiovascular disease and/or hypertension (to prevent interference with psycho-physiological measurements);
  • - Those who suffer from an endocrine disorder, e.g. diabetes mellitus (to prevent interference with cortisol measures);
  • - Smoking > 20 cigarettes per week (to prevent interference with cortisol measures);
  • - No current use of corticosteroid containing medication, including ointments (to prevent interference with cortisol measures);
  • - Subjects who are not literate in Dutch;
  • - Subjects who have an uncorrectable hearing or vision problem;
  • - Age < 18 years

研究者

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