Martinez Diego A, Tsalatsanis Athanasios, Yalcin Ali, Zayas-Castro José L, Djulbegovic Benjamin
Department of Emergency Medicine, Johns Hopkins University, 5801 Smith Avenue Baltimore, Baltimore, 21209, MD, USA.
USF Health Program for Comparative Effectiveness Research, Department of Internal Medicine, University of South Florida, 12901 Bruce B. Downs Blvd., MDC 27, Tampa, FL, 33612, USA.
Trials. 2016 Feb 24;17(1):106. doi: 10.1186/s13063-016-1227-2.
The administrative process associated with clinical trial activation has been criticized as costly, complex, and time-consuming. Prior research has concentrated on identifying administrative barriers and proposing various solutions to reduce activation time, and consequently associated costs. Here, we expand on previous research by incorporating social network analysis and discrete-event simulation to support process improvement decision-making.
We searched for all operational data associated with the administrative process of activating industry-sponsored clinical trials at the Office of Clinical Research of the University of South Florida in Tampa, Florida. We limited the search to those trials initiated and activated between July 2011 and June 2012. We described the process using value stream mapping, studied the interactions of the various process participants using social network analysis, and modeled potential process modifications using discrete-event simulation.
The administrative process comprised 5 sub-processes, 30 activities, 11 decision points, 5 loops, and 8 participants. The mean activation time was 76.6 days. Rate-limiting sub-processes were those of contract and budget development. Key participants during contract and budget development were the Office of Clinical Research, sponsors, and the principal investigator. Simulation results indicate that slight increments on the number of trials, arriving to the Office of Clinical Research, would increase activation time by 11 %. Also, incrementing the efficiency of contract and budget development would reduce the activation time by 28 %. Finally, better synchronization between contract and budget development would reduce time spent on batching documentation; however, no improvements would be attained in total activation time.
The presented process improvement analytic framework not only identifies administrative barriers, but also helps to devise and evaluate potential improvement scenarios. The strength of our framework lies in its system analysis approach that recognizes the stochastic duration of the activation process and the interdependence between process activities and entities.
与临床试验启动相关的管理流程被批评为成本高、复杂且耗时。先前的研究主要集中在识别管理障碍并提出各种解决方案以缩短启动时间,从而降低相关成本。在此,我们通过纳入社会网络分析和离散事件模拟来扩展先前的研究,以支持流程改进决策。
我们搜索了佛罗里达州坦帕市南佛罗里达大学临床研究办公室启动行业赞助临床试验的管理流程的所有运营数据。我们将搜索范围限制在2011年7月至2012年6月期间启动和激活的试验。我们使用价值流图描述该流程,使用社会网络分析研究各个流程参与者之间的相互作用,并使用离散事件模拟对潜在的流程修改进行建模。
管理流程包括5个子流程、30项活动、11个决策点、5个循环和8个参与者。平均激活时间为76.6天。限速子流程是合同和预算制定子流程。合同和预算制定期间的关键参与者是临床研究办公室、赞助商和主要研究者。模拟结果表明,到达临床研究办公室的试验数量略有增加,将使激活时间增加11%。此外,提高合同和预算制定的效率将使激活时间减少28%。最后,合同和预算制定之间更好的同步将减少批量文档处理所花费的时间;然而,总激活时间不会得到改善。
所提出的流程改进分析框架不仅识别管理障碍,还有助于设计和评估潜在的改进方案。我们框架的优势在于其系统分析方法,该方法认识到激活过程的随机持续时间以及流程活动和实体之间的相互依存关系。