Clinical & Transitional Research Support

临床

基本信息

批准号：
7712888
负责人：
RICHARD W SERNA
金额：
$ 21.46万
依托单位：
UNIV OF MASSACHUSETTS MED SCH WORCESTER
依托单位国家：
美国
项目类别：
财政年份：
2008
资助国家：
美国
起止时间：
2008-07-01 至 2010-06-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7712888
关键词：
Address Area Basic Science Behavior Behavioral Clinical Clinical Research Cognitive Collaborations Consent Critiques Databases Developmental Disabilities Diagnostic Dimensions Doctor of Medicine Doctor of Philosophy Effectiveness Ensure Funding Goals Health Human Individual Information Resources Interdisciplinary Study Language Mental Retardation Mental Retardation and Developmental Disabilities Research Centers Numbers Participant Population Preparation Procedures Protocols documentation Purpose Quality Control Range Rate Recruitment Activity Research Research Ethics Committees Research Personnel Research Project Grants Research Support Resources Scientist Score Screening procedure Services Source Specialist Support of Research Testing Training Translational Research Vulnerable Populations base experience interest multidisciplinary programs

项目摘要

CLINICAL AND TRANSLATIONAL RESEARCH SUPPORT Kathleen Braden, M.D., Richard W. Serna, Ph.D., & Edward I. Ginns, M.D., Ph.D. Introduction to Revised Proposal This is a revision of a proposal that was submitted with our 2002 application (priority score: 190). That revision built on many areas of strength noted in its predecessor (submitted with the 2000 application), and was apparently judged a noteworthy improvement. Despite a generally positive review, however, aspects of the 2002 proposal were insufficiently clear and/or not adequately defended, leading to certain reviewer concerns and a less-than-"outstanding" rating. What follows will summarize strengths noted in our past reviews, the reviewer concerns, and the steps taken in this revised proposal to address those concerns. Strengths (2000/2002 proposals combined) 1. Centralized participant recruitment 2. Centralized management of IRB and consent procedures 3. Procedures for maintaining contact with participants and referral sources 4. Central database with desktop access for investigators 5. Specialized participant preparation (e.g., mock scanner) 6. Inclusion of behavioral specialist to assist with preliminary training 7. Ample resources for accomplishing the Core's aims 8. Provision of health screen for participants 9. An interdisciplinary research review team 10. Addition of applied behavior analysts

临床和转化研究支持 Kathleen Braden，医学博士、Richard W. Serna，博士和 Edward I. Ginns，医学博士、哲学博士修订提案简介这是我们 2002 年申请中提交的提案的修订版（优先级分数：190）。那修订建立在其前身（与 2000 年申请一起提交）中指出的许多优势领域的基础上，显然被认为是一个值得注意的改进。尽管获得了普遍积极的评价，但 2002年提案的某些方面不够明确和/或没有得到充分辩护，导致某些问题审稿人的担忧和低于“优秀”的评级。以下将总结以下内容中指出的优势我们过去的审查、审查者关注的问题以及本修订提案中为解决这些问题而采取的步骤的担忧。优势（2000/2002 年提案合并） 1. 集中招募参与者 2. IRB和同意程序的集中管理 3. 与参与者和推荐来源保持联系的程序 4. 可供调查人员桌面访问的中央数据库 5. 专门的参与者准备（例如，模拟扫描仪） 6. 聘请行为专家协助初步培训 7. 实现核心目标的充足资源 8. 为参与者提供健康检查 9. 跨学科研究评审小组 10.增加应用行为分析师