Enhancing Equity in Clinical Research: A Multifaceted Proposal for Spondyloarthritis.

Maureen Dubreuil,Elizabeth D Ferucci,Hani El-Gabalawy,Sarfaraz Hasni,Edith M Williams
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Abstract

Clinical research advances medical knowledge and improves healthcare outcomes. However, disparities in research participation hinder progress. The Unmet Research Needs in Spondyloarthritis Conference IV highlighted critical insights and strategies to enhance equity in clinical research. Talks focused on engaging underrepresented communities and addressing disparities in rheumatic diseases, particularly spondyloarthritis (SpA), to ensure research results are generalizable and inclusive. Disparities in SpA management, such as greater back pain severity among Black and Hispanic Americans and sex-based differences in pain management, emphasize the need for equitable research. Dr. Elizabeth Ferucci discussed the racial disparities in rheumatologic care, highlighting the importance of early access to rheumatologists and culturally informed primary care to improve outcomes. Dr. Hani El-Gabalawy's talk on engaging Indigenous communities stressed the importance of community consent and reciprocal benefits. Dr. Sarfaraz Hasni's presentation on mitigating disparities in research participation underscored the need for inclusive practices and strategies to promote diverse representation. Finally, Dr. Edith Williams emphasized institutional approaches to fostering equity, including diverse recruitment practices and institutional review board alignment with diversity priorities. Strategies to enhance equity in clinical research include community engagement, addressing logistical barriers to participation, and ensuring diverse research teams. These approaches can dismantle barriers for underrepresented communities, making research more accessible and reflective of the broader population. The SpA research community must commit to creating structures that foster inclusivity, ensuring medical advancements benefit all populations, especially historically underrepresented groups. The principles and strategies proposed serve as a roadmap for achieving equity in SpA research.
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加强临床研究的公平性:脊柱关节炎的多方面建议。
临床研究能促进医学知识的发展,改善医疗保健成果。然而,研究参与方面的差距阻碍了研究的进展。第四届脊柱关节炎未满足研究需求会议强调了加强临床研究公平性的重要见解和策略。会议重点讨论了如何让代表性不足的社区参与进来,以及如何解决风湿性疾病,尤其是脊柱关节炎(SpA)中存在的差异,以确保研究成果具有普遍性和包容性。脊柱关节炎治疗中存在的差异,如美国黑人和西班牙裔美国人背痛的严重程度更高,以及疼痛治疗中的性别差异,都强调了公平研究的必要性。Elizabeth Ferucci博士讨论了风湿病治疗中的种族差异,强调了及早就诊风湿病医生和具有文化背景的初级治疗对改善治疗效果的重要性。Hani El-Gabalawy 博士关于土著社区参与的演讲强调了社区同意和互惠互利的重要性。Sarfaraz Hasni 博士关于缩小研究参与差距的发言强调了采取包容性做法和战略以促进多元化代表的必要性。最后,Edith Williams 博士强调了促进公平的机构方法,包括多元化招聘实践和机构审查委员会与多元化优先事项保持一致。加强临床研究公平性的策略包括社区参与、解决参与的后勤障碍以及确保研究团队的多元化。这些方法可以为代表性不足的群体扫除障碍,使研究更容易获得并反映更广泛的人群。SpA 研究界必须致力于创建促进包容性的结构,确保医学进步惠及所有人群,尤其是历史上代表性不足的群体。所提出的原则和战略是实现 SpA 研究公平的路线图。
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Prologue: Spondyloarthritis Unmet Research Needs Conference IV. Enhancing Equity in Clinical Research: A Multifaceted Proposal for Spondyloarthritis. Are There Disease Endotypes in Axial Spondyloarthritis and How Would We Define Them? Unmet Needs in Spondyloarthritis: Understanding and Managing Chronic Pain. Unmet Needs in Spondyloarthritis: Pathogenesis, Clinical Trial Design, and Nonpharmacologic Therapy.
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