NCT04161677已完成不适用
Mitigation Investigation for Spinal Manipulation Treatments (MIST) - Part 3: Continued Assessment & Feasibility of an Electronic Active Surveillance Reporting System
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 161
- 试验地点
- 1
- 主要终点
- follow-up questionnaire
研究概览
简要总结
This study will seek to describe and understand adverse events (AE) severity ratings.
详细描述
Using an explanatory mixed methods design, three different quantitative methods 1. severity ratings based on a series of questions, 2. severity rating based on severity terms, and 3. severity based on definitions will be used to conduct a feasibility study on understanding adverse event reporting system.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Cross Sectional
入排标准
- 年龄范围
- 18 Years 至 65 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Health patients
排除标准
- 未提供
结局指标
主要结局
follow-up questionnaire
时间窗: 7-10 days after visit
Severity rating based on definitions questionnaire
Pre-screening questionnaire
时间窗: 5-10 minute
Severity rating based on a series of questionnaire
Post-survey
时间窗: Immediately after visit
Severity rating based on severity term questionnaire
次要结局
未报告次要终点
研究者
研究点 (1)
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