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临床试验/NCT05695469
NCT05695469已完成不适用

The Impact of Smart Resuscitation Glove (ResuGlove) as Chest Compression Feedback Devices During CPR Training: Feasibility Study of the Device Under Development

University of Turku1 个研究点 分布在 1 个国家目标入组 29 人开始时间: 2023年5月23日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
29
试验地点
1
主要终点
Average Chest compression depth

研究概览

简要总结

The goal of this simulation-based randomized trial is to assess if the newly proposed ResuGlove can improve the quality of chest compressions during CPR training of laypersons and inexperienced health professionals. The main questions it aims to answer are:

  1. To determine if the newly developed wearable resuscitation gloves will improve the quality of chest compression during simulation-based CPR training
  2. To determine the learnability and usability of the ResuGlove using the System Usability Scale (SUS) questionnaire

Participants will be randomly assigned into two equal groups the ResuGlove group (group 1) vs the traditional CPR group (Group 2). The investigators will compare the quality of chest compression between these two groups. On the same day, participants will be asked about the learnability and usability of ResuGlove using the System Usability Scale (SUS questionnaire.

详细描述

AIM OF THE STUDY:

This study is part of an upgoing project to develop smart resuscitation gloves (ResuGlove) that help evaluate the quality of chest compressions during CPR training. The ResuGlove are smart-textile-based wearable technologies expected to provide real-time audiovisual feedback on chest compression quality, including compression depth, compression rate and chest recoil.

This feasibility study aims to evaluate if the newly proposed ResuGloves can significantly improve the quality of chest compressions compared to traditional CPR during simulated cardiac arrest. Besides, researchers will evaluate the learnability and usability of ResuGloves using the System Usability Scale (SUS) questionnaire.

HYPOTHESIS:

Hypothesis 1: ResuGlove will significantly improve the quality of chest compressions compared to the traditional CPR during simulated cardiac arrest Hypothesis 2: Research participants will positively rate the learnability and usability of the ResuGloves under development.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Other
盲法
None

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

  • Nursing student from Turku University of Applied Sciences
  • Students have a minimum of basic life support training
  • Participants should be able to understand and communicate in English

排除标准

  • Participants must not have previous experiences in actual patient resuscitation.
  • Participants who are not able to understand and communicate in English
  • Students with known cardiac/pulmonary diseases, back pain, and wrist problems

结局指标

主要结局

Average Chest compression depth

时间窗: At zero time point (first round) and crossover at 30 minutes (second round)

Chest compression depth is one of the most critical components of quality CPR. The current International Liaison Committee on Resuscitation (ILCOR) guidelines recommended a chest compression depth of 5-6 cm for improved outcomes.

Average chest compression rate

时间窗: At zero time point (first round) and crossover at 30 minutes (second round)

The compression rate is another essential component of quality CPR. The current International Liaison Committee on Resuscitation (ILCOR) guidelines recommended a chest compression rate of 100 to 1200 per minute for improved outcomes.

Proportion of chest recoil

时间窗: At zero time point (first round) and crossover at 30 minutes (second round)

Complete chest release (recoil) between each compression is essential to allow the heart to accumulate blood to be pumped during compressions. Therefore, the International Liaison Committee on Resuscitation (ILCOR) guidelines recommended complete chest recoil (100%) during CPR for a better outcome.

次要结局

  • The proportion of correct compression depth(At zero time point (first round) and crossover at 30 minutes (second round)p)
  • Learnability and usability of the ResuGlove under development(At the end of the second round (30 to 40 minutes))
  • The proportion of correct compression rate(At zero time point (first round) and crossover at 30 minutes (second round))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Desale Tewelde Kahsay

Doctoral researcher

University of Turku

研究点 (1)

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