Health Literate Organizations: Are Clinical Trial Sites Equipped to Recruit Minority and Limited Health Literacy Patients?

Jennifer Livaudais-Toman, Nancy J Burke, Anna Napoles, Celia P Kaplan
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Abstract

Background: Racial/ethnic minority patients are less likely than non-Latino white patients to participate in cancer clinical trials. A key barrier to participation is limited health literacy which is more common among minorities. At the organizational level, it is important that clinical trials sites become better equipped to recruit minority patients by expanding their organizational health literacy including language competency and outreach efforts. We explored the characteristics of clinical trial sites that are associated with these health literate behaviors.

Methods: We identified 353 breast clinical trials recruiting participants in 2006 from four states (California, Florida, Illinois, and New York) through the National Cancer Institute Physician Data Query system. From October 2008 to November 2009, we contacted one research team member (RTM) from each site for a telephone survey to assess the site's health literate characteristics.

Results: Of 233 RTMs who responded, 93% were female and 89% were US-born. Overall, 48% of sites offered supplementary trial information, 80% offered materials to assist with patient navigation and 45% reported outreach efforts. Lower percentages offered information in other languages while 65% offered professional interpretation services. Sites with >10% limited English proficiency (LEP) patients were more likely than their counterparts to offer consent forms (OR=3.13, 1.36-7.19) and supplementary information about trials in other languages (OR=2.52, 1.15-5.52). Sites with diverse patient populations (>10% Latino) were also more likely than less diverse sites to engage in outreach (OR=1.97, 1.07-3.60), to offer consent forms (OR=2.72, 1.38-5.36), supplementary information about trials (OR=2.58, 1.24-5.36), and materials to improve patient navigation (OR=2.50, 1.22-5.13) in other languages.

Conclusions: Efforts to recruit diverse participants were limited. Practice type and diversity of patient population were associated with sites' efforts to accommodate these characteristics, suggesting that sites were responsive to the needs of their patients when diversity was prevalent.

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健康素养组织:临床试验机构是否准备好招募少数族裔和健康素养有限的患者?
背景:与非拉丁裔白人患者相比,少数种族/族裔患者参与癌症临床试验的可能性较低。参与的一个主要障碍是健康知识有限,这在少数族裔中更为常见。在组织层面,临床试验机构必须通过扩大其组织健康素养,包括语言能力和外联工作,更好地招募少数族裔患者。我们探讨了与这些健康素养行为相关的临床试验机构的特点:我们通过国家癌症研究所医生数据查询系统确定了 2006 年在四个州(加利福尼亚州、佛罗里达州、伊利诺伊州和纽约州)招募参与者的 353 项乳腺临床试验。从 2008 年 10 月到 2009 年 11 月,我们联系了每个试验点的一名研究小组成员(RTM)进行电话调查,以评估该试验点的健康素养特征:在 233 名做出回复的 RTM 中,93% 为女性,89% 在美国出生。总体而言,48%的医疗点提供了补充试验信息,80%提供了协助患者导航的材料,45%报告了外展工作。提供其他语言信息的比例较低,而提供专业口译服务的比例为 65%。与其他医疗机构相比,英语水平有限(LEP)患者比例大于 10% 的医疗机构更有可能提供同意书(OR=3.13,1.36-7.19)和其他语言的试验补充信息(OR=2.52,1.15-5.52)。与不太多元化的医疗机构相比,拥有多元化患者群体(拉丁裔患者比例大于10%)的医疗机构更有可能开展外展活动(OR=1.97,1.07-3.60)、提供同意书(OR=2.72,1.38-5.36)、试验补充信息(OR=2.58,1.24-5.36)和其他语言的患者导航材料(OR=2.50,1.22-5.13):招募不同参与者的努力有限。实践类型和患者群体的多样性与医疗机构为适应这些特征所做的努力有关,这表明当多样性普遍存在时,医疗机构能够满足患者的需求。
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