跳至主要内容
临床试验/NCT04141124
NCT04141124已完成不适用

Effects of Relaxing Breathing Combined With Biofeedback on the Performance and Stress of Residents During a High-fidelity Simulation Session.

Claude Bernard University2 个研究点 分布在 1 个国家目标入组 156 人开始时间: 2019年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
156
试验地点
2
主要终点
Performance during HFS

研究概览

简要总结

The harmful effects of stress on health professionals are expressed both in terms of their health (physical or mental) and the quality of work (reduced memory capacity, deterioration in patient care). These adverse effects highlight the importance of implementing effective coping strategies and/or early learning of stress management methods in medical training programs.

Relaxation breathing techniques coupled with heart rate variability (HRV) biofeedback is one of the new techniques used to reduce the stress level.

No research has yet tested the effects of HRV induced by relaxation breathing technique before managing a simulated critical situation.

详细描述

This is a randomized, controlled study conducted at the university simulation centre in healthcare of Lyon, France. The high-fidelity simulation (HFS) will be used as a research tool and the topics included will be the HFS residents summoned to critical care situations as part of their training curriculum. The study has received prior approval from the UCBL1. Ethics Committee. After information (protocol and objective of the study), signature of consent, and one minute of relaxing breathing training, the residents as active participants in HFS, will be included in the study. They will be equipped with Hexoskin® jackets collecting heart rate, heart rate variability, breathing rate continuously and an Empathica® connected watch for continuous measurement of electrodermal activity. Then each resident will be randomized into one of the three intervention groups that are:

  • a relaxing breathing exercise coupled with biofeedback
  • a breathing exercise without biofeedback
  • a control occupation (observation of normal biological results). Each intervention will last five minutes and will be conducted between the briefing and the scenario.

Main objective :

The objective of this study is to compare during HFS, the performance of residents during critical care scenarios. The performance analysis will be performed by two independent and blinded evaluators, based on the video recordings of scenarios. The overall performance will be the addition of technical skills (specific rating grid for each scenario on 100 pts) and non-technical skills assessed by the OTTAWA GRS grid (adjusted to 100 pts).

Secondary objectives :

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)

盲法说明

Intervention will not be observed by outcomes assessor Performance will be evaluated on video recording after the simulation

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

  • Adult person
  • Registered in specialized diploma of medical training.
  • Invited for a high-fidelity simulation session at the Lyon university simulation center.
  • Have signed an informed consent form.

排除标准

  • pregnant woman

结局指标

主要结局

Performance during HFS

时间窗: day 0: during the HFS

Technical specific performance for each scenario. Non-technical performance (with Ottawa GRS Grid).

次要结局

  • psychological stress consequences(0: during the HFS)
  • Psychological stress(0: during the HFS)
  • Physiological stress(day 0: during the HFS)
  • Individual psychological characteristics(0: during the HFS)

研究者

发起方
Claude Bernard University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Lilot Marc

principal investigator

Claude Bernard University

研究点 (2)

Loading locations...

相似试验

Effects of Relaxing Breathing Combined With... | 临床试验