Effect of Fatigue on Regional Anaesthesia Task
The Effect of Fatigue on Regional Anaesthesia Task Performance Among Anaesthetists: a Rater-blinded Randomised Controlled Crossover Trial
The adverse effects of sleep related fatigue are significant, impacting on doctors' health, wellbeing, performance and ultimately their safety and that of their patients'.
Trainees are at an increased risk of fatigue because they routinely, and are increasingly, working long hours, and exposed to excessive and high intensity workloads. With increasing numbers of patient consultations, there is a higher risk of making poorer quality clinical decisions (i.e. decision fatigue). The excessive workloads experienced by doctors can cause fatigue through the requirement for sustained attention over long periods of time, particularly when performing complex and mentally demanding tasks. Our main objective is to study the difference between the fatigued and non-fatigued state of anaesthetists and on their ability to perform an ultrasound-guided peripheral nerve blockade task. We hypothesise that fatigue will result in a clinically significant reduction in the objective structured assessment scores of anaesthetists who are performing an ultrasound-guided peripheral nerve blockade task compared to their scores when they are non-fatigued.
研究概览
研究类型
注册 (预期的)
阶段
- 不适用
联系人和位置
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
1. Anaesthetists of ST3 grade and above with previous experience of performing an ultrasound guided peripheral nerve block.
Exclusion Criteria:
- Previous experience of gaze control training or eye-tracking software applied to medical interventions.
- No previous experience of performing an ultrasound guided peripheral nerve block.
学习计划
研究是如何设计的?
设计细节
- 主要用途:放映
- 分配:随机化
- 介入模型:交叉作业
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
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实验性的:Fatigue Group
The trial will recruit trainee anaesthetists of ST3 grade or higher who take part in a resident night-shift rota at Nottingham University Hospitals NHS Trust.
Participants will undergo baseline psychometric testing to measure baseline mood.
There will be a series of questions to ascertain levels of fatigue.
All participants will then be asked to perform a standardised ultrasound-guided peripheral nerve blockade task using a high fidelity bench-top phantom model.
Performance in this task will be independently assessed using a previously-validated scoring tool by two raters blinded to participant group allocation.
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The intervention will be assessing the participant in a fatigued state compared to a non fatigued state
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有源比较器:Non Fatigued group
The non fatigued group will be asked to perform the same series of questions and tasks after a night at home with no work duties or commitments
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The intervention will be assessing the participant in a fatigued state compared to a non fatigued state
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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composite error scoring within a regional anaesthesia performance task
大体时间:6 months
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establish a comparison of mean composite error scores (CES) between participants in group F (fatigued state) and Group A (non-fatigued state) when performing a standardised ultrasound guided regional anaesthesia task.
CES can range from 0 to 100. the higher the score the more negative the performance of the candidate.
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6 months
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Global rating score (GRS)
大体时间:6 months
|
establish a comparison of mean Global rating scale (GRS) between participants in group F (fatigued state) and Group A (non-fatigued state) when performing a standardised ultrasound guided regional anaesthesia task.
The GRS ranges from a score of 7 to a score of 35.
The higher the score the better the performance.
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6 months
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Task completion time
大体时间:6 months
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Compare the mean time in seconds taken by the participants in Group F and Group A to complete the standardised UGRA task.
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6 months
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Reliability of the composite error score (CES) and global rating scale (GRS)
大体时间:6 months
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calculate the intra-class correlation (ICC) and Cronbach's alpha co-efficient and their associated standard error of the mean (SEM, %).
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6 months
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Eye tracking metrics
大体时间:6 months
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All eye tracking-derived secondary outcome measures listed below will be calculated (and summed to create a total) for each UGRA assessment using the following pre-defined areas of interest: the ultrasound machine screen ('US screen'); their hands, the needle, the US transducer or the cadaveric model ('tools'); and any other area outside the US screen or tools ('other').
This is measures on a numerical scale on the number of times there is deviation and gaze away from the screen.
The lower the number the better the performance by the candidate.
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6 months
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合作者和调查者
调查人员
- 首席研究员:David Hewson, MBBS、University Hospitals of Nottingham
研究记录日期
研究主要日期
学习开始 (预期的)
初级完成 (预期的)
研究完成 (预期的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
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研究美国 FDA 监管的设备产品
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