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A step towards equitable clinical trial recruitment: a protocol for the development and preliminary testing of an online prostate cancer health information and clinical trial matching tool

机译:迈向公平的临床试验招聘的一步:在线前列腺癌健康信息和临床试验匹配工具的开发和初步测试协议

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BackgroundRecruitment of a diverse participant pool to cancer clinical trials is an essential component of clinical research as it improves the generalizability of findings. Investigating and piloting novel recruitment strategies that take advantage of ubiquitous digital technologies has become an important component of facilitating broad recruitment and addressing inequities in clinical trial participation. Equitable and inclusive recruitment improves generalizability of clinical trial outcomes, benefiting patients, clinicians, and the research community. The increasing prevalence of online connectivity in the USA and use of the Internet as a resource for medical information provides an opportunity for digital recruitment strategies in cancer clinical trials. This study aims to measure the acceptability, preliminary estimates of efficacy, and feasibility of the Trial Library intervention, an Internet-based cancer clinical trial matching tool. This study will also examine the extent to which the Trial Library website, designed to address the linguistic and literacy needs of broader patient populations, influences patient-initiated conversations with physicians about clinical trial participation.MethodsThis is a study protocol for a non-randomized, single-arm pilot study. This is a mixed methods study design that utilizes the statistical analysis of quantitative survey data and the qualitative analysis of interview data to assess the participant experience with the Trial Library intervention. This study will examine (1) acceptability as a measure of participant satisfaction with this intervention, (2) preliminary measure of efficacy as a measure of proportion of participants with documented clinical trial discussion in the electronic medical record, and (3) feasibility of the intervention as a measure of duration of clinical visit.DiscussionThe principles that informed the design of the Trial Library intervention aim to be generalizable to clinical trials across many disease contexts. From the ground up, this intervention is built to be inclusive of the linguistic, literacy, and technological needs of underrepresented patient populations. This study will collect essential preliminary data prior to a multi-site randomized clinical trial of the Trial Library intervention.Trial registrationThis study has received institutional approval from the Committee of Human Subjects Research at the University of California, San Francisco.
机译:背景技术参与癌症临床试验的多样化参与者群是临床研究的重要组成部分,因为它提高了研究结果的可推广性。利用无处不在的数字技术调查和试行新颖的招募策略已成为促进广泛招募和解决临床试验参与不平等问题的重要组成部分。公平和包容的招募提高了临床试验结果的可推广性,使患者,临床医生和研究界受益。在美国,在线连接的日益普及以及互联网作为医学信息资源的使用为癌症临床试验中的数字招聘策略提供了机会。这项研究旨在衡量基于互联网的癌症临床试验匹配工具试验库干预的可接受性,有效性的初步估计和可行性。这项研究还将研究旨在满足更广泛患者群体的语言和素养需求的Trial Library网站在多大程度上影响了患者与医生就临床试验参与进行的对话。方法这是一项针对非随机,单臂飞行员研究。这是一种混合方法研究设计,利用定量调查数据的统计分析和访谈数据的定性分析来评估参与者在试验图书馆干预下的经验。这项研究将研究(1)接受程度,以此衡量参与者对该干预的满意度;(2)有效性的初步度量,作为衡量参与者在电子病历中有书面临床试验讨论的比例;以及(3)干预是衡量临床就诊持续时间的一种方法。讨论为试验库干预设计提供依据的原则旨在将其推广到许多疾病情况下的临床试验。从根本上讲,该干预措施旨在将代表性不足的患者人群的语言,素养和技术需求包括在内。该研究将在试验图书馆干预的多站点随机临床试验之前收集基本的初步数据。试验注册该研究已获得美国加利福尼亚大学旧金山分校人类研究委员会的机构批准。

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