Effect of E-learning Training on National Institutes of Health Stroke Scale (NIHSS) and Modified Rankin Scale (mRS) Assessment Performance: a Web-based Randomized Controlled Trial
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 120
- 试验地点
- 1
- 主要终点
- Performance on a NIHSS 50-item quiz
研究概览
简要总结
The goal of this web-based randomized clinical trial is to evaluate whether an e-learning training program improves the accuracy of National Institutes of Health Stroke Scale (NIHSS) and modified Rankin Scale (mRS) assessments among practicing paramedics in French-speaking Switzerland who have not previously received formal training in these scales.
The main questions it aims to answer are:
- Does e-learning training improve performance on a standardized NIHSS assessment quiz compared with no prior training?
- Does e-learning training improve the accuracy of mRS assessment using case-based clinical vignettes compared with no prior training?
Researchers will compare paramedics who complete the NIHSS and mRS e-learning modules before assessment (intervention group) with paramedics who complete the assessments without prior training (control group) to determine whether e-learning training leads to higher assessment performance scores.
Participants will:
- Provide electronic informed consent via a secure web-based platform
- Be randomly assigned to either the intervention group or the control group
- Complete either the e-learning modules before assessment or the assessments before training, depending on group allocation
- Complete an online NIHSS quiz and mRS case-based vignettes
- Receive access to the NIHSS and mRS e-learning modules by the end of the study
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- Double (Investigator, Outcomes Assessor)
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
- •Holding a paramedic title (recognized in Switzerland)
- •Currently actively practicing in Switzerland
- •Fluent in French (all study material will be provided in French)
排除标准
- •Previously completed formal training on either the NIHSS or the mRS.
研究组 & 干预措施
Control group
Control group: Participants will first complete the NIHSS quiz and mRS case vignettes without prior training.
Intervention group
Participants will follow the e-learning modules (NIHSS and mRS).
干预措施: Educational intervention (Other)
结局指标
主要结局
Performance on a NIHSS 50-item quiz
时间窗: From enrollment to the end of the study path in a timeframe of maximum 4 weeks.
The primary outcome will be the performance on a NIHSS 50-item quiz consisting in 3 full assessments of a patient (3x15 items) plus 5 general questions (each question scores 1 point if correct, maximum total of 50 points).
次要结局
- Performance of mRS assessment(From enrollment to the end of the study path in a timeframe of maximum 4 weeks.)
研究者
Stuby Loric
Principal Investigator
Geneve TEAM Ambulances
