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Exploration of the beliefs and experiences of Aboriginal people with cancer in Western Australia: a methodology to acknowledge cultural difference and build understanding

机译:探索西澳大利亚州原住民癌症患者的信仰和经验:承认文化差异并建立理解的方法

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Background Aboriginal Australians experience poorer outcomes, and are 2.5 times more likely to die from cancer than non-Aboriginal people, even after adjustment for stage of diagnosis, cancer treatment and comorbidities. They are also less likely to present early as a result of symptoms and to access treatment. Psycho-social factors affect Aboriginal people's willingness and ability to participate in cancer-related screening and treatment services, but little exploration of this has occurred within Australia to date. The current research adopted a phenomenological qualitative approach to understand and explore the lived experiences of Aboriginal Australians with cancer and their beliefs and understanding around this disease in Western Australia (WA). This paper details considerations in the design and process of conducting the research. Methods/Design The National Health and Medical Research Council (NHMRC) guidelines for ethical conduct of Aboriginal research were followed. Researchers acknowledged the past negative experiences of Aboriginal people with research and were keen to build trust and relationships prior to conducting research with them. Thirty in-depth interviews with Aboriginal people affected by cancer and twenty with health service providers were carried out in urban, rural and remote areas of WA. Interviews were audio-recorded, transcribed verbatim and coded independently by two researchers. NVivo7 software was used to assist data management and analysis. Participants' narratives were divided into broad categories to allow identification of key themes and discussed by the research team. Discussion and conclusion Key issues specific to Aboriginal research include the need for the research process to be relationship-based, respectful, culturally appropriate and inclusive of Aboriginal people. Researchers are accountable to both participants and the wider community for reporting their findings and for research translation so that the research outcomes benefit the Aboriginal community. There are a number of factors that influence whether the desired level of engagement can be achieved in practice. These include the level of resourcing for the project and the researchers' efforts to ensure dissemination and research translation; and the capacity of the Aboriginal community to engage with research given other demands upon their time.
机译:背景技术即使调整了诊断阶段,癌症治疗和合并症,澳大利亚原住民的结局也较差,死于癌症的可能性是非原住民的2.5倍。他们也不太可能因出现症状而提早出现并获得治疗。心理社会因素影响原住民参与癌症相关筛查和治疗服务的意愿和能力,但迄今为止,在澳大利亚尚未对此进行探索。当前的研究采用现象学定性方法来理解和探索澳大利亚原住民患有癌症的生活经验,以及他们对西澳大利亚州(WA)对这种疾病的信仰和理解。本文详细介绍了进行研究的设计和过程中的注意事项。方法/设计遵循了美国国家卫生与医学研究委员会(NHMRC)关于原住民研究道德行为的指南。研究人员承认土著人过去的研究经验,他们热衷于在与他们进行研究之前建立信任和建立关系。在西澳州的城市,农村和偏远地区,对遭受癌症影响的原住民进行了30次深入访谈,对卫生服务提供者进行了20次深入访谈。采访由两名研究人员进行音频记录,逐字记录和独立编码。 NVivo7软件用于协助数据管理和分析。参加者的叙述分为大类,以便确定关键主题,并由研究小组进行讨论。讨论和结论土著研究特有的关键问题包括:研究过程必须基于关系,尊重,在文化上适当并包括土著人民。研究人员对参与者和更广泛的社区负责,要求他们报告其发现并进行翻译,以使研究成果对原住民社区有利。有许多因素会影响实践中是否可以达到所需的参与程度。这些包括项目的资源水平以及研究人员为确保传播和研究翻译所做的努力;以及其他原住民社区根据时间要求进行研究的能力。

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