The association of medical mistrust, clinical trial knowledge, and perceived clinical trial risk with willingness to participate in health research among historically marginalized individuals living in New York City.

Isabel Inez Curro, Laura C Wyatt, Victoria Foster, Yousra Yusuf, Sonia Sifuentes, Perla Chebli, Julie A Kranick, Simona C Kwon, Chau Trinh-Shevrin, Madison N LeCroy
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Abstract

Medical mistrust, clinical trial knowledge, and clinical trial risk impact research participation, yet are rarely studied among racial and ethnic groups. Data were from a cross-sectional survey (n = 1,788). Multinomial logistic regression models examined associations of medical mistrust, clinical trial knowledge, and clinical trial risk with willingness to participate in health research (Yes, No, Unsure) among Chinese, Korean, South Asian, Haitian, North American Latiné, South American Latiné, and Southwest Asian and North African (SWANA) NYC residents with one model per group Overall, 46.1% of participants reported willingness to participate, ranging from 35.8% (Chinese participants) to 58.7% (South Asian participants). Increased mistrust was associated with less willingness among Chinese (OR: 1.06, 95%CI: 1.00, 1.12) and South American Latiné (OR: 1.15, 95%CI: 1.01, 1.30) participants; more willingness among Haitian participants (OR: 0.87, 95%CI: 0.81, 0.94); more uncertainty among Korean (OR: 1.13, 95%CI: 1.05, 1.22), South Asian (OR: 1.07 95%CI: 1.01, 1.12), and North American Latiné (OR: 1.18, 95%CI: 1.09, 1.27) participants; and less uncertainty among Haitian (OR: 0.91, 95%CI: 0.84, 0.99) and SWANA (OR: 0.91, 95%CI:0.86, 0.97) participants. Knowledge was associated with more willingness for Haitian participants (OR: 2.77, 95%CI: 1.15, 6.65), less willingness for Chinese participants (OR: 0.55, 95%CI: 0.34, 0.88), and more uncertainty among South Asian (OR: 2.09, 95%CI: 1.07, 4.07) and SWANA (OR: 2.71, 95%CI: 1.21, 6.03) participants. Some risk and more willingness were linked for South American Latiné participants (OR: 0.14, 95%CI: 0.02, 0.85). Associations varied by group. Studying diverse groups advances equitable research representation.

医疗不信任、临床试验知识和感知临床试验风险与参与健康研究意愿的关系在纽约市历史上被边缘化的个体中。
医疗不信任、临床试验知识和临床试验风险影响研究参与,但很少在种族和族裔群体中进行研究。数据来自横断面调查(n = 1788)。多元逻辑回归模型检验了华人、韩国人、南亚人、海地人、北美拉丁人、南美拉丁人、西南亚和北非(SWANA)纽约市居民的医疗不信任、临床试验知识和临床试验风险与参与健康研究意愿(是、否、不确定)的关系,每组一个模型,总体而言,46.1%的参与者报告了参与意愿。从35.8%(中国参与者)到58.7%(南亚参与者)不等。在中国(OR: 1.06, 95%CI: 1.00, 1.12)和南美拉丁美洲(OR: 1.15, 95%CI: 1.01, 1.30)参与者中,不信任的增加与意愿的减少有关;海地参与者的意愿更高(OR: 0.87, 95%CI: 0.81, 0.94);韩国(OR: 1.13, 95%CI: 1.05, 1.22)、南亚(OR: 1.07, 95%CI: 1.01, 1.12)和北美拉丁裔(OR: 1.18, 95%CI: 1.09, 1.27)参与者的不确定性更大;海地(OR: 0.91, 95%CI: 0.84, 0.99)和SWANA (OR: 0.91, 95%CI:0.86, 0.97)参与者的不确定性较小。海地参与者(OR: 2.77, 95%CI: 1.15, 6.65),中国参与者(OR: 0.55, 95%CI: 0.34, 0.88),南亚参与者(OR: 2.09, 95%CI: 1.07, 4.07)和SWANA参与者(OR: 2.71, 95%CI: 1.21, 6.03)的不确定性与知识相关。南美拉丁参与者的一些风险和更多的意愿相关(OR: 0.14, 95%CI: 0.02, 0.85)。关联因群体而异。研究不同的群体可以促进公平的研究代表性。
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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