Somayaji Darryl, Cloyes Kristin Gates
Author Affiliations: The Phyllis F. Cantor Center, Dana-Farber Cancer Institute/University of Massachusetts Boston (Dr Somayaji); School of Nursing, The University of Utah, Salt Lake City (Dr Gates Cloyes).
Cancer Nurs. 2015 Mar-Apr;38(2):133-44. doi: 10.1097/NCC.0000000000000144.
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.
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.
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.
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 positive/negative tensions between self, family, and community responsibilities.
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.
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.
非裔美国人参与癌症临床试验的人数不足已被视为一个关键问题。与种族、身份和权力相关的历史互动可能导致医疗保健和研究参与方面持续存在不平等。
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作为癌症研究受试者参与研究的信念。
开展了三个非裔美国人焦点小组讨论,参与者包括从未参与过癌症研究的人、参与过的人以及被邀请但拒绝参与的人(n = 16)。讨论聚焦于他们对癌症研究的看法以及作为研究受试者的实际或潜在参与情况。数据采用结构化和归纳编码方法进行编码。
在研究、种族、权力和身份方面出现了恐惧和宿命论,且与更广泛的历史和社会问题相关,而非仅仅是个人的想法或感受。参与者描述了对未知、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正负张力。
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起来。恐惧、宿命论以及当前和历史关系会影响人们如何看待自己作为研究受试者的身份,并可能影响他们参与癌症研究的决定。
认识到包括种族和种族主义在内的复杂因素如何导致健康差距,可能会让护士和其他医疗保健提供者更好地理解个人、社区和组织层面的历史、社会和文化动态如何影响获得癌症研究的机会以及参与癌症研究的情况。