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使用移动应用程序和频闪眼镜进行视觉认知训练干预对帕金森病患者的可行性:一项试点随机对照试验的结果

The feasibility of a visuo-cognitive training intervention using a mobile application and exercise with stroboscopic glasses in Parkinson's: Findings from a pilot randomised controlled trial.

作者信息

Das Julia, Barry Gill, Walker Richard, Vitorio Rodrigo, Celik Yunus, McDonald Claire, Storey Bryony, Oman Paul, Morris Rosie, Stuart Samuel

机构信息

Department of Sport, Exercise & Rehabilitation, Northumbria University, Newcastle upon Tyne, United Kingdom.

Northumbria Healthcare NHS Foundation Trust, North Tyneside General Hospital, North Shields, United Kingdom.

出版信息

PLOS Digit Health. 2024 Dec 18;3(12):e0000696. doi: 10.1371/journal.pdig.0000696. eCollection 2024 Dec.

Abstract

BACKGROUND

There is currently no pharmacological treatment for visuo-cognitive impairments in Parkinson's disease. Alternative strategies are needed to address these non-motor symptoms given their impact on quality of life. Novel technologies have potential to deliver multimodal rehabilitation of visuo-cognitive dysfunction, but more research is required to determine their feasibility in Parkinson's.

OBJECTIVE

To determine the feasibility and preliminary efficacy of a home-based, technological visuo-cognitive training (TVT) intervention using a mobile application and exercise with stroboscopic glasses compared to non-technological care in people with Parkinson's.

METHODS

This 18-month, parallel, two-arm pilot trial took place between July 2021-December 2022. Participants were community-dwelling individuals with a diagnosis of Parkinson's, aged over 50 years. Participants were randomly allocated to one of two active four-week interventions, TVT (n = 20) or standard care (SC) (n = 20). A physiotherapist delivered 8 home visits over 4 weeks, lasting 45-60 mins. Participants were evaluated at baseline and then on completion of the intervention. Primary outcomes were feasibility of the study design and intervention (recruitment/retention, adherence, assessment time scale, equipment and safety). Exploratory outcomes included assessments of cognitive, visual, clinical and motor function. (Blinding of participants was not possible due to the nature of the intervention).

RESULTS

The recruitment rate was 60% (40/67), and the retention rate was 98% (39/40). Adherence to both arms of the intervention was high, with participants attending 98% of visits in the TVT group and 96% of visits in the SC group. 35% (9/20) of participants in the TVT group experienced mild symptoms associated with use of the stroboscopic glasses which included dizziness, queasiness and unsteadiness. There were minimal between group differences, with both interventions having positive effects on a variety of clinical, cognitive, and physical performance outcomes.

CONCLUSIONS

Our findings suggest that home-based TVT with a physiotherapist is feasible in people with Parkinson's and could provide an alternative approach to addressing cognitive and motor dysfunction in this population. We make recommendations for future trials and invite ensuing studies to improve upon the design and utilise stroboscopic visual training and digital tools to investigate this emerging area of multimodal rehabilitation. This trial was prospectively registered at ISRCTN (registration number: ISRCTN46164906; https://doi.org/10.1186/ISRCTN46164906).

摘要

背景

目前帕金森病的视觉认知障碍尚无药物治疗方法。鉴于这些非运动症状对生活质量的影响,需要采取其他策略来解决这些问题。新技术有潜力为视觉认知功能障碍提供多模式康复治疗,但还需要更多研究来确定其在帕金森病中的可行性。

目的

与非技术护理相比,确定使用移动应用程序和频闪眼镜进行家庭式技术视觉认知训练(TVT)干预对帕金森病患者的可行性和初步疗效。

方法

这项为期18个月的平行双臂试点试验于2021年7月至2022年12月进行。参与者为社区居住的帕金森病诊断患者,年龄超过50岁。参与者被随机分配到两种为期四周的积极干预措施之一,即TVT组(n = 20)或标准护理组(SC)(n = 20)。一名物理治疗师在4周内进行8次家访,每次持续45 - 60分钟。在基线时以及干预完成后对参与者进行评估。主要结局是研究设计和干预的可行性(招募/保留、依从性、评估时间尺度、设备和安全性)。探索性结局包括对认知、视觉、临床和运动功能的评估。(由于干预的性质,无法对参与者进行盲法)。

结果

招募率为60%(40/67),保留率为98%(39/40)。两组干预的依从性都很高,TVT组参与者的就诊率为98%,SC组为96%。TVT组35%(9/20)的参与者出现了与使用频闪眼镜相关的轻微症状,包括头晕、恶心和不稳定感。组间差异极小,两种干预对各种临床、认知和身体表现结局都有积极影响。

结论

我们的研究结果表明,由物理治疗师进行的家庭式TVT对帕金森病患者是可行的,并且可以为解决该人群的认知和运动功能障碍提供一种替代方法。我们为未来的试验提出了建议,并邀请后续研究改进设计,利用频闪视觉训练和数字工具来研究这个新兴的多模式康复领域。该试验已在国际标准随机对照试验编号注册库(ISRCTN)进行前瞻性注册(注册号:ISRCTN46164906;https://doi.org/10.1186/ISRCTN46164906)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c64/11654989/4f2b5fba5b57/pdig.0000696.g001.jpg

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