Abstract PO-081: Cancer clinical trial access during the COVID-19 pandemic

Ashithkumar Beloor Suresh, Subecha Dahal, Christopher E. Gantz, A. López
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Abstract

Introduction: Cancer clinical trial conduction during the COVID-19 pandemic required a rapid move to virtual engagement to support participant and research team safety. We were faced with the challenge of translating our approach from in-person to virtual engagement for recruitment, enrollment, and delivery of the study intervention. We present our strategies to conduct cancer clinical trials focused on cancer risk reduction during the COVID-19 pandemic. Subject Recruitment: Our multimodal approach utilized online platforms and established approaches like posters, flyers, and collaborating with community health workers to recruit participants. Our virtual engagement strategies include direct outreach to potential participants via email, the electronic medical record (EMR), and social media. Contact via email and the EMR was guided by study-defined eligibility criteria. Social media outreach was through institutional Twitter, Facebook, and video channel accounts. Twitter posts and chats were employed. Enrollment: e-consenting and remote consenting processes were instituted via REDCAP. Delivery of the Educational Risk Reduction Intervention: We also conducted the intervention using the Zoom platform and through a recorded video of the educational risk reduction intervention, which is shared with the participant via REDCAP. Challenges: As documented by others, the greatest challenge to virtual engagement is lack of internet access and lack of digital literacy. These factors have a greater impact on underserved populations, including the elderly, those with low socioeconomic status, those located farther from the cancer center, and racially/ethnically diverse populations. Conclusion: By translating study outreach and processes to virtual engagement, we were able to facilitate clinical trial access across diverse community subgroups and support subject participation in clinical trials during the COVID-19 pandemic.
PO-081: COVID-19大流行期间癌症临床试验准入
导论:在COVID-19大流行期间进行的癌症临床试验需要快速转向虚拟参与,以支持参与者和研究团队的安全。我们面临着将我们的方法从面对面转换为虚拟参与的挑战,用于招募、注册和研究干预的交付。我们提出了在2019冠状病毒病大流行期间开展癌症临床试验的战略,重点是降低癌症风险。受试者招募:我们的多模式方法利用在线平台和海报、传单等既定方法,并与社区卫生工作者合作招募参与者。我们的虚拟参与策略包括通过电子邮件、电子病历(EMR)和社交媒体直接联系潜在参与者。通过电子邮件和电子病历进行联系,以研究定义的资格标准为指导。通过机构Twitter、Facebook和视频频道账户进行社交媒体宣传。使用Twitter帖子和聊天。入组:通过REDCAP建立电子同意和远程同意流程。降低教育风险干预的交付:我们还使用Zoom平台进行干预,并通过录制的教育风险干预视频,通过REDCAP与参与者分享。挑战:正如其他人所记录的那样,虚拟参与的最大挑战是缺乏互联网接入和缺乏数字素养。这些因素对服务不足的人群有更大的影响,包括老年人,社会经济地位低的人,远离癌症中心的人,以及种族/民族多样化的人群。结论:通过将研究外展和流程转化为虚拟参与,我们能够促进不同社区亚组的临床试验准入,并支持受试者在COVID-19大流行期间参与临床试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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