CORE--PATIENT COORDINATION AND ASSESSMENT

核心——患者协调和评估

• 批准号: 6108887
• 负责人: DEBORAH Ann PEARSON
• 金额: $ 16.82万
• 依托单位: UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON
• 依托单位国家: 美国
• 财政年份: 1999
• 资助国家: 美国
• 起止时间: 1999-03-01 至 2000-02-29
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6108887
• 关键词: Hispanic Americans; autism; behavior test; biomedical facility; clinical research; data collection; ethnic group; human subject; interview; medical outreach /case finding; patient care management; problem solving; volunteer

The purpose of the Patient Coordination and Assessment Core Module (PCACM-CORE B) is to facilitate the participation of human subjects in Program Project research, in particular, Projects I and II. Specific aims are as follows: Aim 1: To provide assessment, eligibility determination, and enrollment of potential participants into Project 1 (neurobehavioral project) and Project II (neuroimaging project); Aim 2: To recruit potential participants for the Program project, while maintaining and expanding liaison with community agencies such as parent groups, mental health agencies, and schools, in order to increase the participant recruitment base for this program of research; Aim 3: Maintain participant enrollment in the Program project and prevent attrition. Aim 4: Collect clinical data for comparison with data from Projects I and II; Aim 5: Provide culturally-based translation of parent-report measures to allow participation of children from Spanish-speaking families and other minority individuals in protocols. The PCACM will serve as a central mechanism for the management of all aspects of human subjects' participation including screening, enrollment, scheduling, transitions between projects, problem resolution, and oversight of informed consent and human subjects protection.

患者协调和评估核心模块的目的 （PCACM-CORE B）是为了促进人类受试者参与 计划 项目研究，特别是项目 I 和 II。具体的 目标如下： 目标 1：提供评估、资格确定和注册 项目 1（神经行为项目）的潜在参与者以及 项目二（神经影像项目）； 目标 2：招募该计划项目的潜在参与者，同时 保持和扩大与家长等社区机构的联系 团体、心理健康机构和学校，以增加 本研究计划的参与者招募基地； 目标 3：维持计划项目的参与者注册并 防止磨损。 目标 4：收集临床数据以与项目 I 的数据进行比较 和二； 目标 5：提供基于文化的家长报告措施翻译 允许来自西班牙语家庭和其他国家的儿童参与 协议中的少数群体。 PCACM 将作为管理所有项目的中央机制 人类受试者参与的各个方面，包括筛选、 注册、日程安排、项目之间的转换、问题 知情同意和人类受试者的决议和监督 保护。