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.

PLOS digital health Pub Date : 2024-12-18 eCollection Date: 2024-12-01 DOI:10.1371/journal.pdig.0000696
Julia Das, Gill Barry, Richard Walker, Rodrigo Vitorio, Yunus Celik, Claire McDonald, Bryony Storey, Paul Oman, Rosie Morris, Samuel Stuart
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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).

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使用移动应用程序和频闪眼镜进行帕金森病视觉认知训练干预的可行性:一项试点随机对照试验的结果。
背景:目前还没有针对帕金森病视觉认知障碍的药物治疗。考虑到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。新技术有可能实现视觉认知功能障碍的多模式康复,但需要更多的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,确定基于家庭的、使用移动应用程序和带频闪眼镜运动的技术视觉认知训练(TVT)干预在帕金森病患者中的可行性和初步效果。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。参与者是年龄在50岁以上的帕金森氏症患者。参与者被随机分配到两种积极的为期四周的干预措施之一,TVT (n = 20)或标准治疗(n = 20)。一名物理治疗师在4周内进行了8次家访,每次持续45-60分钟。参与者在基线进行评估,然后在干预完成时进行评估。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)。探索性结果包括认知、视觉、临床和运动功能的评估。(由于干预的性质,不可能对参与者进行盲法)。结果:入组率为60%(40/67),留用率为98%(39/40)。两组干预的依从性都很高,TVT组98%的参与者参加了就诊,SC组96%的参与者参加了就诊。TVT组中35%(9/20)的参与者经历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。两组之间的差异很小,两种干预措施对各种临床、认知和身体表现结果都有积极影响。结论:我们的研究结果表明,在物理治疗师的指导下,以家庭为基础的TVT对帕金森病患者是可行的,并且可以为解决这一人群的认知和运动功能障碍提供另一种方法。我们对未来的试验提出建议,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一新兴的多模式康复领域。该试验在ISRCTN前瞻性注册(注册号:ISRCTN46164906;https://doi.org/10.1186/ISRCTN46164906)。
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