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首页> 外文期刊>BMC Medical Ethics >An effective multisource informed consent procedure for research and clinical practice: an observational study of patient understanding and awareness of their roles as research stakeholders in a cancer biobank
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An effective multisource informed consent procedure for research and clinical practice: an observational study of patient understanding and awareness of their roles as research stakeholders in a cancer biobank

机译:研究和临床实践的有效多源知情同意程序:对患者了解和了解其作为癌症生物库中研究利益相关者的作用的观察性研究

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Background Efforts to improve patients’ understanding of their own medical treatments or research in which they are involved are progressing, especially with regard to informed consent procedures. We aimed to design a multisource informed consent procedure that is easily adaptable to both clinical and research applications, and to evaluate its effectiveness in terms of understanding and awareness, even in less educated patients. Methods We designed a multisource informed consent procedure for patients’ enrolment in a Cancer Institute Biobank (CRO-Biobank). From October 2009 to July 2011, a total of 550 cancer patients admitted to the Centro di Riferimento Oncologico IRCCS Aviano, who agreed to contribute to its biobank, were consecutively enrolled. Participants were asked to answer a self-administered questionnaire aim at exploring their understanding of biobanks and their needs for information on this topic, before and after study participation. Chi-square tests were performed on the questionnaire answers, according to gender or education. Results Of the 430 patients who returned the questionnaire, only 36.5% knew what a biobank was before participating in the study. Patients with less formal education were less informed by some sources (the Internet, newspapers, magazines, and our Institute). The final assessment test, taken after the multisource informed consent procedure, showed more than 95% correct answers. The information received was judged to be very or fairly understandable in almost all cases. More than 95% of patients were aware of participating in a biobank project, and gave helping cancer research (67.5%), moral obligation, and supporting cancer care as main reasons for their involvement. Conclusions Our multisource informed consent information system allowed a high rate of understanding and awareness of study participation, even among less-educated participants, and could be an effective and easy-to-apply model for others to consider to contribute to a well-informed decision making process in several fields, from clinical practice to research. Further studies are needed to explore the effects on the study comprehension by each source of information, and by other sources suggested by participants in the questionnaire.
机译:背景技术正在努力提高患者对他们自己所参与的医学治疗或研究的了解,尤其是在知情同意程序方面。我们旨在设计一种易于适应临床和研究应用的多源知情同意程序,并评估即使在教育程度较低的患者中,其在理解和认识方面的有效性。方法我们为癌症研究机构生物库(CRO-Biobank)中的患者注册设计了多源知情同意程序。从2009年10月到2011年7月,共有550名癌症患者入选了同意为其生物库捐款的RCCS Aviano中心。要求参与者回答一项自我管理的问卷,目的是在研究参与之前和之后,探索他们对生物库的理解以及对有关此主题的信息的需求。根据性别或教育程度,对问卷答案进行卡方检验。结果在返回问卷的430位患者中,只有36.5%的人在参与研究之前知道生物库的内容。受过较少正规教育的患者通过某些来源(互联网,报纸,杂志和我们的研究所)了解的信息较少。在多源知情同意程序之后进行的最终评估测试显示出超过95%的正确答案。几乎在所有情况下,都认为收到的信息是非常或相当可以理解的。超过95%的患者意识到参与了一个生物库项目,并给予了帮助进行癌症研究(67.5%),道德义务和支持癌症护理作为其参与的主要原因。结论我们的多源知情同意信息系统即使在受教育程度较低的参与者中也能提高对研究参与的理解和认识,并且可以成为其他人考虑做出有助于做出明智决定的有效且易于应用的模型从临床实践到研究的多个领域的制作过程。需要进一步的研究,以探索每种信息来源以及问卷参与者建议的其他来源对研究理解的影响。

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