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通过虚拟现实干预促进健康参与者的放松和减轻压力:一项非劣效性随机对照试验的研究方案。

Facilitating relaxation and stress reduction in healthy participants through a virtual reality intervention: study protocol for a non-inferiority randomized controlled trial.

机构信息

Department of Clinical Psychology and Psychotherapy, University of Siegen, Obergraben 23, 57072, Siegen, Germany.

Bender Institute of Neuroimaging, Justus Liebig University, Giessen, Otto-Behaghel-Str. 10 H, 35394, Giessen, Germany.

出版信息

Trials. 2022 May 9;23(1):380. doi: 10.1186/s13063-022-06307-8.

Abstract

BACKGROUND

Repeated or chronic stress is considered a major source of disease, in terms of both somatic and mental illnesses. The prevention of stress-related disease by interventions for relaxation has thus increased societal relevance. In this randomized controlled non-inferiority trial, we will compare a newly developed virtual reality (VR) environment for relaxation to an active control group applying a freely chosen relaxation method. To test if our VR environment supports relaxation in a situation of acute stress, a standardized stress induction protocol will precede the relaxation phase.

METHODS

One hundred healthy participants will be recruited from the University of Siegen and randomly assigned to the VR or the active control group that will be free to choose their own relaxation strategy. The multi-sensory VR includes visual, acoustic, and haptic features to induce a strong feeling of presence. The laboratory testing will comprise a baseline measurement, a stress induction, a relaxation intervention, and a recovery measurement. The primary outcomes are self-reported stress and relaxation measured with a visual analog scale (VAS) at pre- and post-baseline, at the start, middle, and end of the stress induction, at pre- and post-relaxation, at pre- and post-recovery, and in the evening of testing. Secondary outcomes are the physiological parameters, namely heart rate and heart rate variability, tonic skin conductance level as well as the number of non-specific skin conductance responses, systolic and diastolic blood pressure and respiratory rate recorded during the four experimental phases as well as state mood, and state rumination assessed at four time points (pre- and post-stress, post-relaxation, and in the evening of testing). Finally, post-event processing will be assessed after relaxation and in the evening of testing. Repeated measures ANOVAs will be performed to test for statistical effects of group, time, and group × time interaction.

DISCUSSION

The newly developed, multi-sensory VR offers an intervention for relaxation without prior training. Its immersive character might increase efficacy compared to other relaxation methods, especially in situations of acute stress. Future directions could be the development of a mobile version of the VR to enhance accessibility for users. To achieve a transfer of training effects to real life, VR components should successively be eliminated until relaxation is practiced without guidance by the VR.

TRIAL REGISTRATION

ISRCTN Registry ISRCTN11162338 . Retrospectively registered on January 22, 2021.

摘要

背景

反复或慢性压力被认为是躯体和精神疾病的主要致病因素。因此,通过放松干预来预防与压力相关的疾病已经引起了社会的广泛关注。在这项随机对照非劣效性试验中,我们将比较一种新开发的虚拟现实(VR)放松环境与应用自由选择的放松方法的主动对照组。为了测试我们的 VR 环境是否在急性应激情况下支持放松,将在放松阶段之前进行标准化应激诱导方案。

方法

将从 Siegen 大学招募 100 名健康参与者,并将其随机分配到 VR 组或主动对照组,主动对照组可以自由选择自己的放松策略。多感觉 VR 包括视觉、听觉和触觉特征,以产生强烈的存在感。实验室测试将包括基线测量、应激诱导、放松干预和恢复测量。主要结果是使用视觉模拟量表(VAS)在基线前后、应激诱导开始时、中间和结束时、放松前、放松后、恢复后以及测试当晚自我报告的应激和放松。次要结果是生理参数,即心率和心率变异性、紧张性皮肤电导率水平以及非特异性皮肤电导率反应的数量,在四个实验阶段记录的收缩压和舒张压以及呼吸率,以及在四个时间点评估的状态情绪和状态沉思(应激前后、放松后和测试当晚)。最后,在放松后和测试当晚评估事后处理。将进行重复测量方差分析,以检验组、时间和组×时间交互作用的统计学效果。

讨论

新开发的多感觉 VR 提供了一种无需事先训练的放松干预措施。与其他放松方法相比,它的沉浸式特征可能会提高疗效,特别是在急性应激情况下。未来的方向可以是开发 VR 的移动版本,以提高用户的可及性。为了将训练效果转移到现实生活中,应逐步消除 VR 组件,直到在没有 VR 指导的情况下进行放松练习。

试验注册

ISRCTN 注册处 ISRCTN11162338。于 2021 年 1 月 22 日回顾性注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e47b/9082920/5bffac740541/13063_2022_6307_Fig1_HTML.jpg

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