■患有COVID-19后疾病(PCC)的成年人可能在注意力方面表现出认知障碍,处理速度,记忆,和执行功能。结合认知训练的多模式项目,身体活动和情感任务,例如基于正念的干预措施(MBIs),可以为改善PCC治疗提供合适的替代方案。沉浸式虚拟现实(IVR)是一种有前途的技术,可以增强传统的认知训练,身体活动,和MBIs。IVR技术的使用可能会增加对这些干预措施的参与,并可能增强认知训练的个人益处,锻炼和MBI。当前的研究评估了多模式IVR干预的影响,将其与常规护理干预(对照组)进行比较,为了评估PCC成人的认知和心理健康的变化。我们还旨在评估用户体验因素,如享受、感知到的改进,以及实验组内每个多模态IVR会话后的疲劳。
■将31名有PCC症状的参与者分配到实验组(IVR,n=15)或对照组(常规护理干预,n=16)在准实验设计研究中。多模态IVR干预包括MBI,认知训练和体育锻炼,并在60分钟的小组会议中进行,有5名参与者,一周两次,为期8周(共16个疗程)。全球认知的衡量标准,注意,处理速度,言语情景记忆和主观记忆抱怨(主要措施),在基线和8周后(干预后)评估抑郁和焦虑症状以及疲劳(次要指标).
■组间(组)和组内(后评估前)混合的ANOVA揭示了全球认知中的显着组*时间相互作用,简单的注意,处理速度,记忆和抑郁症状,具有较大的效应大小(p<0.05;部分η2>0.14)。执行功能也有轻微显著的组*时间相互作用(p=0.05)。随访分析分别比较各组干预前和干预后的结果,结果显示实验组的整体认知能力显著提高,处理速度,记忆和抑郁症状,而对照组没有明显的前后变化。Friedman检验显示时间的显著主效应(χ2(2)=6.609,p=0.04),从一开始就逐渐增加了乐趣,到了中期,然后进入最后的会议。此外,在整个干预过程中,感知到的改善分数仍然很高,患者报告的疲劳水平在整个干预期间没有显著波动.
■据我们所知,以前的研究没有结合认知训练,在PCC成人中使用IVR范式进行体育锻炼和MBI。尽管有其固有的局限性,我们的发现标志着通过创新使用新技术和多模式方法改善PCC认知和心理健康结果的开创性一步.这项第一项研究应该伴随着更广泛的,随机临床试验旨在进一步探索和完善这些干预措施。
UNASSIGNED: Adults with Post-COVID-19 Condition (PCC) may show cognitive impairments in attention, processing speed, memory, and executive function. Multimodal programs that combine cognitive training, physical activity and emotional tasks, such as mindfulness-based interventions (MBIs), may offer a suitable alternative for improving PCC treatments. Immersive Virtual Reality (IVR) is a promising technology that can enhance traditional cognitive training, physical activity, and MBIs. The use of IVR technology may increase engagement with these interventions and potentially enhance the individual benefits of cognitive training, exercise and MBIs. The current study evaluated the impact of a multimodal IVR intervention, comparing this with a usual care intervention (control group), in order to assess changes in cognition and mental health in adults with PCC. We also aimed to assess user experience factors such as enjoyment, perceived improvement, and fatigue following each multimodal IVR session within the experimental group.
UNASSIGNED: Thirty-one participants with PCC symptoms were assigned to either the experimental group (IVR, n = 15) or the control group (usual care intervention, n = 16) in a quasi-experimental design study. The multimodal IVR intervention consisted of MBI, cognitive training and physical exercise and was delivered in a 60-min group session with 5 participants, twice a week, for 8 weeks (16 sessions in total). Measures of global cognition, attention, processing speed, verbal episodic memory and subjective memory complaints (primary measures), and depressive and anxiety symptoms and fatigue (secondary measures) were assessed at baseline and also after 8 weeks (post-intervention).
UNASSIGNED: Mixed between-group (group) and within-group (pre-post assessments) ANOVAs revealed significant group*time interactions in global cognition, simple attention, processing speed, memory and depressive symptoms, with large effect sizes (p < 0.05; partial η2 > 0.14). There was also a marginally significant group*time interaction for executive function (p = 0.05). Follow-up analyses comparing pre-and post-intervention outcomes for each group separately showed that the experimental group significantly improved in global cognition, processing speed, memory and depressive symptoms, while the control group showed no significant pre-post changes. Friedman tests showed a significant main effect of time (χ2(2) = 6.609, p = 0.04), with a gradual increase in enjoyment from the first, to the mid, and then to the final session. In addition, perceived improvement scores remained high throughout the intervention, and patient-reported fatigue levels did not fluctuate significantly throughout the intervention.
UNASSIGNED: To our knowledge, no previous research has combined cognitive training, physical exercise and MBI using an IVR paradigm in adults with PCC. Despite their inherent limitations, our findings mark a pioneering step toward improving cognition and mental health outcomes in PCC through the innovative use of new technology and multimodal approaches. This first study should be accompanied by more extensive, randomized clinical trials aimed at further exploring and refining these interventions.