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临床试验/NCT07318376
NCT07318376尚未招募不适用

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

Stuby Loric1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2026年4月1日最近更新:
干预措施

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

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

No Intervention

Control group: Participants will first complete the NIHSS quiz and mRS case vignettes without prior training.

Intervention group

Experimental

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

发起方
Stuby Loric
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Stuby Loric

Principal Investigator

Geneve TEAM Ambulances

研究点 (1)

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