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How does the collection of genetic test results affect research participants?

机译:基因测试结果的收集如何影响研究参与者?

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The collection of genetic test results has become routine in clinical research. Yet, there are few data on the impact of this practice. The present study provides the first empirical data that we are aware of on the impact this practice has on research participants. The findings suggest that collection of genetic test results in the research setting increases many individuals' desire to know the results themselves. Some respondents attributed this effect to the fact that the data existed, while others did not want investigators to have information about them that they did not possess. A smaller proportion of respondents assumed that investigators who had collected genetic test results would monitor their clinical significance over time. These respondents were less inclined to want to know their genetic test results once an investigator was aware of them. Investigators and IRBs should recognize these phenomena and address them in the design and conduct of studies which collect genetic information. Published 2007 Wiley-Liss, Inc.
机译:基因测试结果的收集已成为临床研究中的常规方法。但是,关于这种做法的影响的数据很少。本研究提供了我们所知道的关于该实践对研究参与者的影响的第一批经验数据。研究结果表明,在研究环境中收集基因测试结果会增加许多人自己了解结果的愿望。一些受访者将此影响归因于数据存在的事实,而另一些受访者不希望调查人员获得他们不拥有的有关他们的信息。较小比例的受访者认为,收集了基因检测结果的研究者将随着时间的推移监测其临床意义。一旦调查人员知道了这些调查对象,他们就不太愿意了解他们的基因检测结果。研究人员和IRB应该认识到这些现象,并在设计和进行收集遗传信息的研究中加以解决。 2007年出版的Wiley-Liss,Inc.

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