McHugh Claire G, Gottreich Julia R, Kumara Mahima T, Selzer Faith, Collins Jamie E, Losina Elena, Katz Jeffrey N
Orthopaedic and Arthritis Center for Outcomes Research, Department of Orthopedic Surgery, Brigham and Women's Hospital, USA.
Harvard Medical School, USA.
Osteoarthr Cartil Open. 2023 Jan 18;5(1):100337. doi: 10.1016/j.ocarto.2023.100337. eCollection 2023 Mar.
To provide a framework for conducting clinical trial site visits virtually over videoconference, and to report on our experience doing so during the twelve-year follow-up of the Meniscal Tear in Osteoarthritis Research (MeTeOR) trial.
Using published FDA guidance and prior literature, we created a structure for virtual site visits that prioritized monitoring for protocol compliance, safety, and data integrity. We conducted site visits in three stages: preparation for the visit, the virtual meeting itself, and follow-up. The preparation phase involved a review of relevant site-specific documents and a written report on the findings prior to the visit. The virtual visit itself was focused on any questions the site staff had about the pre-visit report, observing a mock study visit, touring physical spaces, and understanding the site staff's work environment. In the follow-up phase, we wrote a post-visit report summarizing the discussion during the visit and feedback given by the coordinating site.
We found that the virtual site visits conducted as part of the MeTeOR trial follow-up ran smoothly. Although we could not directly compare in-person and virtual site visits, site staff unanimously appreciated the efficiency and effectiveness of the virtual site visits. We noted that displaying physical workspaces over videoconferencing was difficult, and a notable drawback to this method.
To our knowledge, this is the first published framework for conducting virtual clinical trial site visits. Conducting these visits virtually confer several advantages in terms of time, money, and efficiency.
提供一个通过视频会议进行临床试验现场访视的框架,并报告我们在骨关节炎半月板撕裂研究(MeTeOR)试验的12年随访期间这样做的经验。
利用美国食品药品监督管理局(FDA)发布的指南和先前的文献,我们创建了一个虚拟现场访视的结构,该结构优先对方案依从性、安全性和数据完整性进行监测。我们分三个阶段进行现场访视:访视准备、虚拟会议本身以及随访。准备阶段包括审查相关的特定现场文件,并在访视前撰写一份关于调查结果的书面报告。虚拟访视本身聚焦于现场工作人员对访视前报告的任何疑问、观察一次模拟研究访视、参观实际空间以及了解现场工作人员的工作环境。在随访阶段,我们撰写了一份访视后报告,总结访视期间的讨论以及协调中心给出的反馈。
我们发现,作为MeTeOR试验随访一部分进行的虚拟现场访视进展顺利。尽管我们无法直接比较面对面访视和虚拟访视,但现场工作人员一致赞赏虚拟访视的效率和效果。我们注意到,通过视频会议展示实际工作空间很困难,这是这种方法的一个明显缺点。
据我们所知,这是首个发表的关于进行虚拟临床试验现场访视的框架。以虚拟方式进行这些访视在时间、资金和效率方面具有诸多优势。