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首页> 外文期刊>Cancer nursing >Cancer Fear and Fatalism How African American Participants Construct the Role of Research Subject in Relation to Clinical Cancer Research
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Cancer Fear and Fatalism How African American Participants Construct the Role of Research Subject in Relation to Clinical Cancer Research

机译:癌症恐惧与宿命论非裔美国人如何建立研究对象在临床癌症研究中的作用

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摘要

Background: Lack of African American participation in cancer clinical trials has been identified as a critical problem. Historical interactions related to race, identity, and power may contribute to continued inequity in healthcare and research participation. Objective: The aim of this study was to explore the perceptions of African Americans regarding cancer and research and how these perceptions shape their beliefs about participating as cancer research subjects. Methods: Three African American focus groups were conducted including people who had never participated in cancer research, those who had, and those who were asked but refused (n = 16). Discussion focused on their perceptions of cancer research and actual or potential participation as research subjects. Data were coded using both structured and inductive coding methods. Results: Fear and fatalism emerged in relation to research, race, power, and identity and were related to larger historical and social issues rather than only individual thoughts or feelings. Participants described fears of the unknown, death, mistrust, conspiracy, and discrimination together with positiveegative tensions between self, family, and community responsibilities. Conclusion: Complex identities linked perceptions of cancer and cancer research with broader historical and cultural issues. Fear, fatalism, and current and historical relationships influence how people perceive themselves as research subjects and may influence their decisions to participate in cancer research. Implication for Practice: Acknowledging how complex factors including race and racism contribute to health disparities may give nurses and other healthcare providers a better appreciation of how historical, social, and cultural dynamics at individual, community, and organizational levels influence access to and participation in cancer research.
机译:背景:缺乏非洲裔美国人参与癌症临床试验已被认为是一个关键问题。与种族,身份和权力有关的历史互动可能会导致医疗保健和研究参与的持续不平等。目的:本研究的目的是探讨非裔美国人对癌症和研究的看法,以及这些看法如何塑造他们对参与癌症研究主题的信念。方法:进行了三个非裔美国人焦点小组讨论,其中包括从未参加癌症研究的人,曾经参加过癌症的人和被要求接受但被拒绝的人(n = 16)。讨论的重点是他们对癌症研究的看法以及作为研究对象的实际或潜在参与。使用结构化和归纳编码方法对数据进行编码。结果:恐惧和宿命论与研究,种族,权力和身份有关,并且与更大的历史和社会问题有关,而不仅仅是个人的思想或感情。参加者描述了对未知,死亡,不信任,阴谋和歧视的恐惧,以及自我,家庭和社区责任之间的积极/消极关系。结论:复杂的身份将对癌症和癌症研究的看法与更广泛的历史和文化问题联系在一起。恐惧,宿命论以及当前和历史的关系会影响人们将自己视为研​​究对象的方式,并可能影响他们参与癌症研究的决定。实践的意义:认识到种族和种族歧视等复杂因素如何导致健康差异,可以使护士和其他医疗保健提供者更好地了解个人,社区和组织层面的历史,社会和文化动态如何影响癌症的获取和参与。研究。

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