Telemedicine's Utility for Augmenting Clinical Trials and Informed Consent TACTIC
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 试验地点
- 1
- 主要终点
- Number of trials participant is enrolled into
研究概览
简要总结
This is a 6 year, Phase I, Clinical Research Protocol to study the feasibility of using a telemedicine system for performing research in a remote hospital system.
详细描述
The UCSD Telemedicine system is a digital video camera system, which can transfer video and audio images from a clinic or emergency room to a remote place where a physician can review images in real time (as they happen). The system uses site independent software to access the camera system from multiple locations. This research study will determine if it is feasible to obtain informed consent for various types of research trials (hypothetical, non-invasive, invasive trails) via telemedicine. Inpatient assessments on participants to complete clinical research case report forms by telemedicine will also by performed.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male/Female, age 18 years or older
- •Clinical neurological focal deficits consistent with stroke
- •Time of onset 3-24 hours and with stable neurological deficit
- •Signed Informed Consent
排除标准
- •Deficits known to be due to non-stroke etiology
- •Time of onset less than 3 hours
- •Patients unable to give consent
结局指标
主要结局
Number of trials participant is enrolled into
时间窗: 5 years
Counting how many patients are enrolled into OTHER clinical trials using a telemedicine technique
次要结局
未报告次要终点
研究者
Brett Meyer
MD
University of California, San Diego