关键词: Informed consent Mixed reality Patient engagement Surgical interventions Surgical outcomes

来  源:   DOI:10.25259/SNI_1021_2023   PDF(Pubmed)

Abstract:
UNASSIGNED: Informed consent is a crucial aspect of modern medicine, but it can be challenging due to the complexity of the information involved. Mixed reality (MR) has emerged as a promising technology to improve communication. However, there is a lack of comprehensive research on the impact of MR on medical informed consent. The proposed research protocol provides a solid foundation for conducting future investigations and developing MR-based protocols that can enhance patients\' understanding and engagement in the decision-making process.
UNASSIGNED: This study will employ a randomized controlled trial design. Two arms will be defined: MR-assisted informed consent (MRaIC) as the experimental arm and conventional informed consent (CIC) as the control arm consent, with 52 patients in each group. The protocol includes the use of questionnaires to analyze the anxiety levels and the awareness of the procedure that the patient is going to perform to study the impact of MRaIC versus CIC before medical procedures.
UNASSIGNED: The study will evaluate the impact of MR on patients\' information comprehension, engagement during the process of obtaining informed consent, emotional reactions, and consent decisions. Ethical concerns will be addressed.
UNASSIGNED: This study protocol provides a comprehensive approach to investigate the impact of MR on medical informed consent. The findings may contribute to a better understanding of the effects of MR on information comprehension, engagement during the process of obtaining informed consent, psychological experience, consent decisions, and ethical considerations. The integration of MR technology has the potential to enhance surgical communication practices and improve the informed consent process.
摘要:
知情同意是现代医学的一个重要方面,但是由于所涉及的信息的复杂性,这可能是具有挑战性的。混合现实(MR)已成为改善通信的有前途的技术。然而,缺乏关于MR对医疗知情同意的影响的全面研究。拟议的研究方案为进行未来的调查和开发基于MR的方案提供了坚实的基础,这些方案可以增强患者对决策过程的理解和参与。
本研究将采用随机对照试验设计。将定义两个臂:MR辅助知情同意(MraIC)作为实验臂和常规知情同意(CIC)作为控制臂同意。每组52例。该方案包括使用问卷来分析焦虑水平和对患者将要执行的程序的认识,以研究医疗程序前MRaICversusCIC的影响。
该研究将评估MR对患者信息理解的影响,在获得知情同意的过程中参与,情绪反应,和同意决定。伦理问题将得到解决。
本研究方案提供了一种全面的方法来调查MR对医疗知情同意的影响。这些发现可能有助于更好地理解MR对信息理解的影响,在获得知情同意的过程中参与,心理体验,同意决定,和道德考虑。MR技术的整合有可能增强手术沟通实践并改善知情同意程序。
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