RESEARCH DESIGN, BIOSTATISTICS AND CLINICAL RESEARCH ETHICS

这个子项目是利用资源的许多研究子项目之一。 由NIH/NCRR资助的中心拨款提供。对子项目的主要支持 子项目的首席调查员可能是由其他来源提供的， 包括美国国立卫生研究院的其他来源。为子项目列出的总成本可能 表示该子项目使用的中心基础设施的估计数量， 不是由NCRR赠款提供给次级项目或次级项目工作人员的直接资金。 A.具体目标 研究设计、生物统计学和临床伦理学的具体目标 (DBRE)计划是：1)支持临床和 翻译研究设计、生物统计分析和临床 加强研究设计，应用研究伦理 适当的生物统计技术，并加强伦理道德 协议的设计和实施，2)培训调查人员 临床和转化性研究设计、生物统计学和临床 通过研讨会、研讨会和个人工作室研究伦理 准备和工作室会议，以及3)与研究互动 RTRN的设计和生物统计组件在进行多个 现场临床和转化性研究。

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. Primary support for the subproject and the subproject's principal investigator may have been provided by other sources, including other NIH sources. The Total Cost listed for the subproject likely represents the estimated amount of Center infrastructure utilized by the subproject, not direct funding provided by the NCRR grant to the subproject or subproject staff. A. Specific Aims Specific aims of the Research Design, Biostatistics and Clinical Ethics (DBRE) Program are: 1) to support all aspects of clinical and translational research design, biostatistical analysis and clinical research ethics by strengthening study designs, applying appropriate biostatistical techniques, and enhancing the ethical design and implementation of protocols, 2) to train investigators in clinical and translational research design, biostatistics, and clinical research ethics through seminars, workshops and individual Studio Prep and Studio sessions, and 3) to interact with the research design and biostatistics components of the RTRN in conducting multi- site clinical and translational research.