Coordinating and monitoring multisite clinical trials that combine pharmacological and behavioral treatments.

Marston E Youngblood, Kelly T Murray, Eric Devine, Patricia K Latham, Sandra Hubatch
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引用次数: 7

Abstract

Objective: Coordination of a large, multicenter Phase 3 clinical trial is critical to the success of the trial. The focus of this article is to describe the special challenges involved in the coordination of the 11 clinical centers conducting the COMBINE clinical trial and to discuss the challenges of monitoring the information collected on the 1,383 participants enrolled in this trial.

Method: The role of the coordinating center in working with the clinical sites is to ensure both high data quality and that the intervention protocol is conducted with appropriate attention paid to patient safety and consistency across sites. To satisfy those goals, a research committee of investigators and coordinating center staff was formed. The committee monitored adverse event reporting, participant safety, recruitment, delivery of the interventions, collection of assessments and completeness and timeliness of transfer of data to the coordinating center. Objective measures of performance were determined for each criterion to provide the principal investigators, study sponsor and Data and Safety Monitoring Board with feedback on conduct of the trial. Site performance as defined by these criteria was evaluated periodically, with both detailed written and verbal feedback provided to each investigator and study coordinator.

Results: The system was successful in detecting sites with performance issues, providing feedback to site personnel and measuring improvement. Study leadership, clinical center staff and coordinating center staff felt that the procedures for identifying and solving performance issues worked well and improved overall performance.

Conclusions: Establishing an organizational structure that provided (1) leadership, (2) a venue for communication, (3) performance criteria and (4) a process for monitoring performance goals and providing feedback has enabled COMBINE to achieve success in reaching these markers of clinical trial practice.

协调和监测结合药理学和行为治疗的多地点临床试验。
目的:大型、多中心iii期临床试验的协调是试验成功的关键。本文的重点是描述进行联合临床试验的11个临床中心的协调所涉及的特殊挑战,并讨论监测该试验中1383名参与者收集的信息所面临的挑战。方法:协调中心在与临床站点合作时的作用是确保高数据质量,并确保干预方案的实施适当关注患者的安全性和跨站点的一致性。为了实现这些目标,成立了一个由调查人员和协调中心工作人员组成的研究委员会。委员会监测了不良事件报告、参与者安全、招募、干预措施的提供、评估的收集以及向协调中心转移数据的完整性和及时性。为每个标准确定了客观的绩效衡量标准,以向主要研究者、研究发起人和数据与安全监测委员会提供有关试验实施的反馈。根据这些标准定义的现场表现定期进行评估,并向每位研究者和研究协调员提供详细的书面和口头反馈。结果:该系统成功地发现了有性能问题的站点,向站点人员提供反馈并衡量改进。研究领导、临床中心工作人员和协调中心工作人员认为,确定和解决绩效问题的程序运作良好,提高了整体绩效。结论:建立一个组织结构,提供(1)领导,(2)沟通场所,(3)绩效标准,(4)监控绩效目标和提供反馈的过程,使COMBINE能够成功地达到这些临床试验实践的标志。
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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