加速药物伙伴关系®精神分裂症项目的样本确定和临床结果测量。

IF 3 Q2 PSYCHIATRY
Jean Addington, Lu Liu, Amy Braun, Andrea Auther, Monica E Calkins, Barbara A Cornblatt, Cheryl M Corcoran, Paolo Fusar-Poli, Melissa J Kerr, Catalina V Mourgues-Codern, Angela R Nunez, Dominic Oliver, Gregory P Strauss, Barbara C Walsh, Luis K Alameda, Celso Arango, Nicholas J K Breitborde, Matthew R Broome, Kristin S Cadenhead, Ricardo E Carrion, Eric Yu Hai Chen, Jimmy Choi, Michael J Coleman, Philippe Conus, Covadonga M Diaz-Caneja, Dominic Dwyer, Lauren M Ellman, Masoomeh Faghankhani, Pablo A Gaspar, Carla Gerber, Louise Birkedal Glenthøj, Leslie E Horton, Christy Hui, Grace R Jacobs, Joseph Kambeitz, Lana Kambeitz-Ilankovic, Matcheri S Keshavan, Sung-Wan Kim, Nikolaos Koutsouleris, Jun Soo Kwon, Kerstin Langbein, Kathryn E Lewandowski, Daniel Mamah, Patricia J Marcy, Daniel H Mathalon, Vijay A Mittal, Merete Nordentoft, Godfrey D Pearlson, Nora Penzel, Jesus Perez, Diana O Perkins, Albert R Powers, Jack Rogers, Fred W Sabb, Jason Schiffman, Jai L Shah, Steven M Silverstein, Stefan Smesny, William S Stone, Andrew Thompson, Judy L Thompson, Rachel Upthegrove, Swapna Verma, Jijun Wang, Heather M Wastler, Alana Wickham, Inge Winter-van Rossum, Daniel H Wolf, Sylvain Bouix, Ofer Pasternak, Rene S Kahn, Carrie E Bearden, John M Kane, Patrick D McGorry, Kate Buccilli, Barnaby Nelson, Martha E Shenton, Scott W Woods, Alison R Yung
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引用次数: 0

摘要

临床确定和临床结果是任何大型多地点研究的关键特征。在ProNET和PRESCIENT研究网络中,加速药物合作伙伴®精神分裂症(AMP®SCZ)临床确定和结果测量小组旨在建立跨这两个研究网络的统一临床评估方案,并定义确定标准和主要和次要终点。除了制定评估方案,AMP SCZ项目这方面的目标是:(1)实施和监督临床培训,确定参与者和临床评估;(2)为精神病风险评估、数据集成和计算技术:数据处理、分析和协调中心(PREDICT-DPACC)提供专家临床意见,用于数据收集、质量控制和临床措施分析的数据准备;(3)为临床数据的收集、分析和报告提供持续支持。本文描述了(1)方案临床终点和结果,(2)临床测量方法选择的基本原理,(3)临床工作人员的广泛培训,(4)为包括英语不是母语的几个地点的多地点研究准备临床测量方法;(5) AMP SCZ观察性研究中测量稳定性随时间的评估,比较基线和2个月随访时的临床评分。观看Jean Addington博士讨论她的工作和这篇文章:https://vimeo.com/1040425281。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Sample ascertainment and clinical outcome measures in the Accelerating Medicines Partnership® Schizophrenia Program.

Clinical ascertainment and clinical outcome are key features of any large multisite study. In the ProNET and PRESCIENT research networks, the Accelerating Medicines Partnership® Schizophrenia (AMP®SCZ) Clinical Ascertainment and Outcome Measures Team aimed to establish a harmonized clinical assessment protocol across these two research networks and to define ascertainment criteria and primary and secondary endpoints. In addition to developing the assessment protocol, the goals of this aspect of the AMP SCZ project were: (1) to implement and monitor clinical training, ascertainment of participants, and clinical assessments; (2) to provide expert clinical input to the Psychosis Risk Evaluation, Data Integration and Computational Technologies: Data Processing, Analysis, and Coordination Center (PREDICT-DPACC) for data collection, quality control, and preparation of data for the analysis of the clinical measures; and (3) to provide ongoing support to the collection, analysis, and reporting of clinical data. This paper describes the (1) protocol clinical endpoints and outcomes, (2) rationale for the selection of the clinical measures, (3) extensive training of clinical staff, (4) preparation of clinical measures for a multisite study which includes several sites where English is not the native language; and (5) the assessment of measure stability over time in the AMP SCZ observational study comparing clinical ratings at baseline and at the 2-month follow up. Watch Dr. Jean Addington discuss her work and this article: https://vimeo.com/1040425281 .

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