Translational Genomics and Community-Driven Research in Australia

Q2 Social Sciences
Fiona Russo, Keri Finlay, Isabella Sherburn, Tiffany Boughtwood, Jane Tiller
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Abstract

The need for community involvement in human translational research has gained international recognition, with a growing consensus on its critical role in ensuring ethical and impactful health outcomes. In Australia, several bodies are beginning to mandate community involvement in research, reflecting this global trend. However, there remains a notable gap in practical guidance on effectively engaging communities, particularly in the emerging field of genomic research. To address this, Australian Genomics, a national collaboration supporting the translation of genomic research into clinical practice, coordinated an initiative called Involve Australia (IA). IA has developed comprehensive guidelines, together with and informed by the needs and perspectives of those directly impacted by genomic research, through surveys, interviews, and public consultations. The IA Guidelines provide practical information for genomic researchers on involving community members effectively and meaningfully in projects to ensure effective research translation, emphasizing the importance of building relationships, setting clear expectations, valuing community contributions, evaluating and reporting on the community involvement process, and translation of research outcomes. The IA Guidelines have been endorsed by various research and patient organizations, demonstrating the growing support for resources in this area. The development and implementation of these guidelines represent a crucial step forward in promoting community involvement in genomic research, setting a precedent for other areas of health and medical research to follow.

Abstract Image

澳大利亚的转化基因组学和社区驱动研究
社区参与人体转化研究的必要性已得到国际承认,其在确保合乎道德和有影响的健康结果方面的关键作用已得到越来越多的共识。在澳大利亚,一些机构开始要求社区参与研究,反映了这一全球趋势。然而,在有效参与社区的实践指导方面,特别是在新兴的基因组研究领域,仍然存在明显的差距。为了解决这个问题,澳大利亚基因组学,一个支持将基因组研究转化为临床实践的国家合作组织,协调了一项名为“澳大利亚参与”(IA)的倡议。基因组研究所通过调查、访谈和公众咨询,与基因组研究直接影响者的需求和观点一起制定了全面的指导方针。IA指南为基因组研究人员提供了实用的信息,使社区成员有效和有意义地参与项目,以确保有效的研究翻译,强调建立关系的重要性,设定明确的期望,重视社区贡献,评估和报告社区参与过程,以及翻译研究成果。该指南已得到各种研究和患者组织的认可,表明对该领域资源的支持日益增加。这些准则的制定和实施是在促进社区参与基因组研究方面向前迈出的关键一步,为其他卫生和医学研究领域树立了先例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Ethics & human research
Ethics & human research Social Sciences-Health (social science)
CiteScore
2.90
自引率
0.00%
发文量
35
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