Kaljee Linda, Antwi Sylvester, Dankerlui Doreen, Harris Donna, Israel Barbara, White-Perkins Denise, Ofori Aboah Valerie, Aduse-Poku Livingstone, Larrious-Lartey Harriet, Brush Barbara, Coombe Chris, Patman La'Toshia, Cawthorne Nayomi, Chue Sophia, Rowe Zachary, Mills Cassandra, Fernando Kurt, Daniels Gwendolyn, Walker Eleanor M, Jiagge Evelyn
Henry Ford Health, Global Health Initiative, Detroit, MI 48202, United States.
Henry Ford Health, Detroit, MI 48202, United States.
JNCI Cancer Spectr. 2025 Jan 3;9(1). doi: 10.1093/jncics/pkae119.
Black/African Americans experience disproportionate cancer burden and mortality rates. Racial and ethnic variation in cancer burden reflects systemic and health-care inequities, cancer risk factors, and heredity and genomic diversity. Multiple systemic, sociocultural, economic, and individual factors also contribute to disproportionately low Black/African American participation in cancer clinical trials.
The Participatory Action for Access to Clinical Trials project used a community-based participatory research approach inclusive of Black/African American community-based organizations, Henry Ford Health, and the University of Michigan Urban Research Center. The project aims were to understand Black/African Americans' behavioral intentions to participate in cancer clinical trials and to obtain recommendations for improving participation. Audio-recorded focus group data were transcribed and coded, and searches were conducted to identify themes and subthemes. Representative text was extracted from the transcripts.
Six community focus group discussions (70 participants) and 6 Henry Ford Health patient/survivor focus group discussions (29 participants) were completed. General themes related to trial participation were identified, including (1) systemic issues related to racism, health disparities, and trust in government, health systems, and clinical research; (2) firsthand experiences with health care and health systems; (3) perceived and experienced advantages and disadvantages of clinical trial participation; and (4) recruitment procedures and personal decision-making processes. Specific recommendations on how to address barriers were obtained.
Community-based participatory research is effective in bringing communities equitably to the table. To build trust, health systems must provide opportunities for patients and communities to jointly identify factors affecting cancer clinical trial participation, implement recommendations, and address health disparities.
黑人/非裔美国人承受着不成比例的癌症负担和死亡率。癌症负担方面的种族和族裔差异反映了系统性和医疗保健方面的不平等、癌症风险因素以及遗传和基因组多样性。多种系统性、社会文化、经济和个人因素也导致黑人/非裔美国人参与癌症临床试验的比例低得不成比例。
“参与临床试验的参与式行动”项目采用了基于社区的参与式研究方法,纳入了以社区为基础的黑人/非裔美国人组织、亨利·福特健康中心和密歇根大学城市研究中心。该项目的目标是了解黑人/非裔美国人参与癌症临床试验的行为意图,并获得改善参与情况的建议。对焦点小组的录音数据进行转录和编码,并进行搜索以确定主题和子主题。从转录本中提取代表性文本。
完成了6次社区焦点小组讨论(70名参与者)和6次亨利·福特健康中心患者/幸存者焦点小组讨论(29名参与者)。确定了与试验参与相关的一般主题,包括:(1)与种族主义、健康差距以及对政府、卫生系统和临床研究的信任相关的系统性问题;(2)医疗保健和卫生系统的第一手经验;(3)临床试验参与的感知和实际优缺点;(4)招募程序和个人决策过程。获得了关于如何解决障碍的具体建议。
基于社区的参与式研究有效地使社区能够公平地参与进来。为了建立信任,卫生系统必须为患者和社区提供机会,共同确定影响癌症临床试验参与的因素,实施建议并解决健康差距问题。