Adverse events reporting in Implementation science clinical trials

项目摘要 我们提出的工作有可能开发差异化的、量身定制的不良事件报告， 实施科学的临床试验设计，特别是如果报告的作用和重点可能不是 使用现有临床试验不良事件报告框架适当满足。从长远来看，这些 这些好处旨在“涓滴”到非洲和其他任何国家的所有实施科学临床试验中， 需要努力确保充分和适当地报告不利的 实施科学临床试验中的事件。我们的研究结果将在当地的政策和专业 发展会议，研究会议和国际研究，如期刊和科学 聚会。

PROJECT SUMMARY Our proposed work has the potential to develop differentiated, tailored adverse event reporting for implementation science clinical trial designs, especially if the role and focus of reporting may not be appropriately met using existing clinical trial adverse event reporting frameworks. Over the long term, these benefits are intended to “trickle” down to all implementation science clinical trials in Africa and any other parts of the world where efforts are required to ensure adequate and appropriate reporting of adverse events in implementation science clinical trials. Our results will be presented at local policy and professional development meetings, research meetings and international research such as journals and scientific gatherings.