通过理解包容性临床试验的障碍和驱动因素促进多样性。

IF 2 4区 医学 Q4 MEDICAL INFORMATICS
Annick de Bruin, Jasmine Masullo, Shalome Sine, Kenneth Getz
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引用次数: 0

摘要

重要性:临床试验参与者的种族和民族多样性,公平的代表性对于加强药物开发过程和促进公平的医疗保健结果非常重要。目的:了解包容性临床试验的障碍和驱动因素,重点关注代表性不足的人群所面临的态度、观念、经历和挑战。设计:一份在线问卷于2023年4月至6月在网上进行,涉及来自54个国家的12017名受访者。这项调查采用了方便的抽样策略。对不同种族和民族的反应进行统计分析比较。环境:本研究在全球范围内进行。调查对象是通过各种患者招募组织、患者倡导团体和合同研究组织招募的。受访者:18岁或以上的成年人,只要收到电子邮件或可以上网,就有资格参与。种族和民族构成包括白人(81%)、西班牙裔/拉丁裔(15%)、黑人/非裔美国人(6%)、亚洲人(6%)和其他种族。暴露:受访者被问及他们对临床研究准入和参与的看法、担忧和经历。主要结果和衡量指标:主要结果包括参与临床研究的障碍、影响对制药公司信任的因素和过去的经验。结果:参与临床研究的障碍因种族而异。亚裔受访者表示,与白人受访者(分别为7%和7%)相比,他们更担心请假(22%)和参加活动所需的时间(19%);结论:研究结果强调需要解决临床试验多样性的障碍,改善代表性不足的社区的试验经验,促进设计更具包容性和以患者为中心的试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Promoting Diversity through an Understanding of Barriers and Drivers for Inclusive Clinical Trials.

Importance: Racially and ethnically diverse, equitable representation among clinical trial participants is important for enhancing the drug development process and promoting equitable healthcare outcomes.

Objective: To understand the barriers and drivers for inclusive clinical trials, focusing on the attitudes, perceptions, experiences, and challenges faced by underrepresented populations.

Design: An online questionnaire was administered online from April to June 2023 and involved 12,017 respondents from 54 countries. This survey utilized a convenience sampling strategy. Statistical analysis was performed to compare responses among racial and ethnic groups.

Setting: The study was conducted globally. Survey respondents were recruited through various patient recruitment organizations, patient advocacy groups, and contract research organizations.

Respondents: Adults 18 years or older who received an email or had online access were eligible to participate. Racial and ethnic composition included White (81%), Hispanic/Latino (15%), Black/African American (6%), Asian (6%), and other ethnicities.

Exposure(s): Respondents were asked about their perceptions, concerns and experiences related to clinical research access and participation.

Main outcome(s) and measure(s): Key outcomes included barriers to clinical research participation, factors influencing trust in pharmaceutical companies and past experiences.

Results: Barriers to clinical research participation varied among ethnic groups. Asian respondents cited concerns about time off work (22%) and time required to participate (19%) more frequently as compared to White respondents (7% and 7%, respectively; p < 0.05). Hispanics expressed higher concerns about time off work (15%) and receiving placebo (10%) as compared to Non-Hispanics (8% and 5%, respectively, p < 0.05). Black and Hispanic respondents placed higher importance on diversity in staff compared to White and non-Hispanic respondents (B: 32%; W: 12%; Hispanic: 22%; Non-Hispanic: 13% p < 0.05). Black, Asian, and Hispanic respondents reported higher levels of disruption in participation related to technology use (Black: 31%; Hispanic: 30%; Asian: 29%) and completing study requirements at home (Black: 32%; Hispanic: 30%; Asian: 26%) as compared to White (13%, 15%; p < 0.05%) and non-Hispanic respondents (14%, 17%; p < 0.05).

Conclusions: The findings highlight the need to address barriers to diversity in clinical trials and improve trial experiences of underrepresented communities, facilitating design of more inclusive and patient-centered trials.

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来源期刊
Therapeutic innovation & regulatory science
Therapeutic innovation & regulatory science MEDICAL INFORMATICS-PHARMACOLOGY & PHARMACY
CiteScore
3.40
自引率
13.30%
发文量
127
期刊介绍: Therapeutic Innovation & Regulatory Science (TIRS) is the official scientific journal of DIA that strives to advance medical product discovery, development, regulation, and use through the publication of peer-reviewed original and review articles, commentaries, and letters to the editor across the spectrum of converting biomedical science into practical solutions to advance human health. The focus areas of the journal are as follows: Biostatistics Clinical Trials Product Development and Innovation Global Perspectives Policy Regulatory Science Product Safety Special Populations
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