Sue Tea C, Churchill Isabella F, Parr Ann M, Tsai Eve C
Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.
Department of Neurosurgery, University of Minnesota, Minneapolis, MN, United States.
Front Neurol. 2025 May 13;16:1587632. doi: 10.3389/fneur.2025.1587632. eCollection 2025.
The underrepresentation of women and racial minorities in clinical trials populations remains a persistent challenge across many medical specialties, including Neurosurgery. A diverse research cohort brings varied perspectives and experiences, which can lead to more innovative solutions to medical problems, generalizable findings, and the foundations to provide culturally competent care to the populations most affected by the condition at hand. The importance of representative Neurotrauma trial populations cannot be overstated, as results are essential to inform decision making and gender and race have both been shown to significantly influence patient outcomes, as seen in the traumatic brain injury and spinal cord injury populations. Although the path towards gender and racial parity in clinical trial participants has been slow, numerous actions have been taken, including the FDA Safety and Innovation Act (2012) and Omnibus Reform Act (2022) on a systemic level. In this paper, we aimed to explore the barriers to and implications of inadequate representation in neurotrauma trials to outline a roadmap towards more diverse trial inclusion and retention. Key strategies moving forward include recruiting a diverse research team, developing flexible study protocols that support the varying needs of individuals of different backgrounds, establishing methods of data analysis that control for social and demographic factors instead of excluding individuals from participating, introducing patient navigators, reflecting on systemically engrained biases, implementing mandatory reporting of gender and race data, establishing and analyzing policies that keep researchers accountable towards goals of inclusive recruitment, and identifying and addressing unique barriers that individuals at the intersection of gender and racial minority status face.
在包括神经外科在内的许多医学专科中,临床试验人群中女性和少数族裔代表不足仍然是一个长期存在的挑战。一个多样化的研究队列带来了不同的观点和经验,这可以带来更多创新的医疗问题解决方案、可推广的研究结果,以及为受当前疾病影响最严重的人群提供具有文化胜任力护理的基础。具有代表性的神经创伤试验人群的重要性再怎么强调也不为过,因为研究结果对于为决策提供依据至关重要,而且性别和种族都已被证明会显著影响患者的治疗结果,这在创伤性脑损伤和脊髓损伤人群中可见一斑。尽管在临床试验参与者中实现性别和种族平等的道路一直很缓慢,但已经采取了许多行动,包括在系统层面上的《美国食品药品监督管理局安全与创新法案》(2012年)和《综合改革法案》(2022年)。在本文中,我们旨在探讨神经创伤试验中代表性不足的障碍及其影响,以勾勒出一条实现更多样化试验纳入和保留的路线图。未来的关键策略包括组建一个多样化的研究团队,制定灵活的研究方案以支持不同背景个体的不同需求,建立控制社会和人口因素的数据分析方法而不是将个体排除在参与之外,引入患者导航员,反思系统中根深蒂固的偏见,实施性别和种族数据的强制报告,制定并分析使研究人员对包容性招募目标负责的政策,以及识别和解决处于性别和少数族裔地位交叉点的个体所面临的独特障碍。