Parkinson’s disease

帕金森病
  • 文章类型: Journal Article
    BACKGROUND: Early, simple predictors for long-term survival in Parkinson\'s disease (PD) may help identify patients at elevated risk and are crucial for more personalized treatment.
    METHODS: This large, retrospective study examined whether higher levodopa equivalent daily dose (LEDD) a year after diagnosis predicts long-term survival.
    RESULTS: Mortality risk was increased among 292 patients receiving ≥ 600 mg LEDD versus 2233 patients receiving < 600 mg LEDD (hazard ratio 1.5; 95% confidence interval 1.3-1.7), particularly among patients aged < 75 years (1.8; 1.4-2.4).
    CONCLUSIONS: In PD, higher LEDD can be an early risk marker of increased mortality, probably because it reflects more severe disease.
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  • 文章类型: Journal Article
    目的:针对苍白球(GPi)的深部脑刺激(DBS)已被证明可以显着改善运动症状,以治疗难治性帕金森病。然而,临床结果的异质性仍然存在,可能是由于GPi内的次优目标识别。通过利用GPi和术后6个月结局的稳健抽样,本研究旨在确定最佳的症状特异性GPiDBS目标.
    方法:在本研究中,作者分析了解剖导联位置和术后6个月,86例接受双侧GPiDBS的患者的双盲结局指标.这些患者是从多中心退伍军人事务部(VA)/美国国家神经疾病和中风研究所(NINDS)合作研究计划(CSP)468研究中选择的,以确定控制整体运动的最佳目标区域(“最佳点”)(联合帕金森氏症评定量表[UPDRS]-III),轴向,震颤,刚性,和运动迟缓症状。将铅坐标归一化到蒙特利尔神经病学研究所空间,并使用留一病人方法确定和验证最佳目标区。
    结果:作者的研究结果表明,UPDRS-III的最佳目标区域具有统计学意义(R=0.37,p<0.001),轴向(R=0.22,p=0.042),刚度(R=0.20,p=0.021),和运动迟缓(R=0.23,p=0.004)症状。这些区域位于GPi的主电机和前电机分区内。有趣的是,这些区域延伸到GPi横向边界之外,进入GPi-苍白球(GPe)层并进入GPe,但是他们没有到达GPI腹侧边界,挑战传统的手术方法基于苍白球切开术。
    结论:利用稳健的数据集,这项研究不仅有效地描述了整体运动改善的特定最佳目标区域,而且还描述了症状子评分。这些见解具有在随后的双侧GPiDBS外科手术中提高靶向精度的潜力。
    OBJECTIVE: Deep brain stimulation (DBS) targeting the globus pallidus interna (GPi) has been shown to significantly improve motor symptoms for the treatment of medication-refractory Parkinson\'s disease. Yet, heterogeneity in clinical outcomes persists, possibly due to suboptimal target identification within the GPi. By leveraging robust sampling of the GPi and 6-month postsurgical outcomes, this study aims to determine optimal symptom-specific GPi DBS targets.
    METHODS: In this study, the authors analyzed the anatomical lead location and 6-month postsurgical, double-blinded outcome measures of 86 patients who underwent bilateral GPi DBS. These patients were selected from the multicenter Veterans Affairs (VA)/National Institutes of Neurological Disorders and Stroke (NINDS) Cooperative Studies Program (CSP) 468 study to identify the optimal target zones (\"sweet spots\") for the control of overall motor (United Parkinson\'s Disease Rating Scale [UPDRS]-III), axial, tremor, rigidity, and bradykinesia symptoms. Lead coordinates were normalized to Montreal Neurological Institute space and the optimal target zones were identified and validated using a leave-one-patient-out approach.
    RESULTS: The authors\' findings revealed statistically significant optimal target zones for UPDRS-III (R = 0.37, p < 0.001), axial (R = 0.22, p = 0.042), rigidity (R = 0.20, p = 0.021), and bradykinesia (R = 0.23, p = 0.004) symptoms. These zones were localized within the primary motor and premotor subdivisions of the GPi. Interestingly, these zones extended beyond the GPi lateral border into the GPi-globus pallidus externa (GPe) lamina and into the GPe, but they did not reach the GPi ventral border, challenging traditional surgical approaches based on pallidotomies.
    CONCLUSIONS: Drawing upon a robust dataset, this research effectively delineates specific optimal target zones for not only overall motor improvement but also symptom subscores. These insights hold the potential to enhance the precision of targeting in subsequent bilateral GPi DBS surgical procedures.
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  • 文章类型: Journal Article
    目的:在不同人群中,帕金森病(PD)与心血管疾病(CVD)死亡率之间的相关性有相互矛盾的报道。因此,研究PD与CVD死亡率之间的关系对于降低前者引起的死亡率至关重要。
    方法:在这项队列调查中,我们纳入了2003年至2018年国家健康和营养检查调查的28,242名参与者.队列中的380例PD是通过记录其报告的处方药中的“抗帕金森病药物”来确定的。通过将队列数据库与国家死亡指数进行交叉引用来确定死亡率结果,最后更新于2019年12月31日。根据《国际疾病分类》第10次修订版,使用一系列诊断代码对心血管疾病死亡率进行分类。使用加权多变量Cox回归分析来检查PD与CVD死亡风险之间的关联。
    结果:共有28,242名成年人被纳入研究[平均年龄,60.156(12.55)年,13,766名男性(48.74%)],中位随访期为89个月.与没有PD的患者相比,患有PD的患者的CVD死亡率的校正HR为1.82(95%CI,1.24-2.69;p=0.002),全因死亡率为1.84(95%CI,1.44-2.33;p<0.001)。在敏感性分析中,PD和CVD死亡率之间的关联是稳健的,在排除在随访2年内死亡的参与者和基线有癌症史的参与者后[HR,1.82(95%CI,1.20-2.75;p=0.005)]。
    结论:PD与美国人群长期心血管疾病死亡率高相关。
    OBJECTIVE: Conflicting results have been reported on the association between Parkinson\'s disease (PD) and cardiovascular disease (CVD) mortality in different populations. Therefore, studying the relationship between PD and CVD mortality is crucial to reduce mortality caused by the former.
    METHODS: In this cohort investigation, we enrolled 28,242 participants from the National Health and Nutrition Examination Survey spanning from 2003 to 2018. The 380 cases of PD in the cohort were identified by documenting \'ANTIPARKINSON AGENTS\' in their reported prescription medications. Mortality outcomes were ascertained by cross-referencing the cohort database with the National Death Index, which was last updated on 31 December 2019. Cardiovascular disease mortality was categorised according to the 10th revision of the International Classification of Diseases by using a spectrum of diagnostic codes. Weighted multivariable Cox regression analysis was used to examine the association between PD and the risk of CVD mortality.
    RESULTS: A total of 28,242 adults were included in the study [mean age, 60.156 (12.55) years, 13,766 men (48.74%)], and the median follow-up period was 89 months. Individuals with PD had an adjusted HR of 1.82 (95% CI, 1.24-2.69; p = 0.002) for CVD mortality and 1.84 (95% CI, 1.44-2.33; p < 0.001) for all-cause mortality compared with those without PD. The association between PD and CVD mortality was robust in sensitivity analyses, after excluding participants who died within 2 years of follow-up and those with a history of cancer at baseline [HR,1.82 (95% CI, 1.20-2.75; p = 0.005)].
    CONCLUSIONS: PD was associated with a high long-term CVD mortality rate in the US population.
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  • 文章类型: Case Reports
    疼痛是帕金森病(PD)的一种常见但治疗不足的症状。这项研究调查了刮沙疗法对PD患者疼痛的影响。
    共有56名PD疼痛患者被随机分为任一实验组(n=28),接受了12次刮沙治疗,或对照组(n=28),无需额外治疗。参与者在基线时接受评估,在第十二发明之后,在2个月的随访时间点。主要结果是KPPS和VAS。次要结果包括UPDRSI-III,PDSS-2,HADS,PDQ-39和血液生物标志物(5-HT,IL-8、IL-10)。
    实验组报告疼痛严重程度显著改善,电机功能,情感障碍,睡眠质量(P<0.05)。此外,观察到5-HT和IL-10的增加趋势以及IL-8的减少趋势。无严重不良事件发生。
    初步研究结果表明,瓜沙疗法对于缓解PD患者的疼痛和改善其他疾病相关症状可能是有效和安全的。
    UNASSIGNED: Pain is a common yet undertreated symptom of Parkinson\'s disease (PD). This study investigated the effect of Gua Sha therapy on pain in patients with PD.
    UNASSIGNED: A total of 56 PD patients with pain were randomized into either the experimental group (n=28), receiving 12 sessions of Gua Sha therapy, or the control group (n=28) without additional treatment. Participants underwent assessment at baseline, after the twelfth invention, and at the 2-month follow-up timepoints. The primary outcome was KPPS and VAS. Secondary outcomes included UPDRS I-III, PDSS-2, HADS, PDQ-39, and blood biomarkers (5-HT, IL-8, IL-10).
    UNASSIGNED: The experimental group reported a significant improvement in pain severity, motor functions, affective disorder, and sleep quality (P < 0.05). Furthermore, increasing trends in both 5-HT and IL-10, as well as decreasing trends in IL-8 were observed. No serious adverse events occurred.
    UNASSIGNED: The preliminary findings suggest that Gua Sha therapy may be effective and safe for alleviating pain and improving other disease-related symptoms in PD patients.
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  • 文章类型: Journal Article
    RolandoToro的Biodanza(SRT)是一种使用运动的治疗策略,音乐,和情感来诱导综合生活体验。本研究旨在探讨为期三个月的SRT干预对运动,认知,帕金森病(PD)患者的行为症状。本研究采用随机组间设计。本研究纳入了28名非痴呆型PD患者。在这些中,14例患者被分配到使用BiodanzaSRT系统的积极治疗组,14例患者被分配到未经治疗的对照组.研究组每周参加一次2hSRT课程,在十二周内完成十二课。所有患者均接受:(i)神经系统检查以测量运动症状的严重程度,balance,移动性,和跌倒的风险,和(Ii)评估认知状态的神经心理学电池,冷漠,抑郁症状,和感知生活质量(QoL),在研究开始时(T0)和12周(T1,舞蹈训练结束)。在T1,我们观察到电机的显着改善(即,运动症状和平衡的严重程度)和认知参数(即,与对照组相比,所有接受治疗的患者的工作记忆和延迟言语记忆)。此外,与对照组相比,所有接受治疗的患者的社会支持维度均有显著改善.在T1未治疗的患者中发现了冷漠增加的趋势。三个月的Biodanza干预显着改善了PD患者的运动参数,认知和QoL状态的平行改善。因此,Biodanza干预可以,在短期内,代表了帕金森病管理的一种有用的个性化医疗干预措施。
    Rolando Toro\'s Biodanza (SRT) is a therapeutic strategy that uses movement, music, and emotions to induce integrative living experiences. The present study aims to explore the efficacy of a three-month SRT intervention on motor, cognitive, and behavioral symptoms in patients with Parkinson\'s disease (PD). This study employed a randomized between-group design. Twenty-eight non-demented PD patients were enrolled in this study. Out of these, fourteen patients were assigned to the active treatment group using the Biodanza SRT system and fourteen to the untreated control group. The study group attended 2 h SRT classes once a week, completing twelve lessons in twelve weeks. All patients underwent: (i) a neurological examination to measure the severity of motor symptoms, balance, mobility, and risk of falls, and (ii) a neuropsychological battery to assess cognitive status, apathy, depressive symptomatology, and perceived quality of life (QoL), at study entry (T0) and at twelve weeks (T1, end of dance training). At T1, we observed a significant improvement in motor (i.e., severity of motor symptoms and balance) and cognitive parameters (i.e., working memory and delayed verbal memory) in all treated patients compared with the controls. Furthermore, a significant improvement in the social support dimension was found in all treated patients compared to the controls. A trend toward increased apathy was found in untreated patients at T1. The three-month Biodanza intervention significantly ameliorated the motor parameters of PD patients, with a parallel improvement in cognitive and QoL status. Hence, Biodanza intervention can, in the short term, represent a useful personalized medical intervention for the management of Parkinson\'s disease.
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  • 文章类型: Journal Article
    背景:随着医疗保健领域技术集成的增加,重要的是要了解新兴技术在减少对医疗保健系统的需求方面可能发挥的好处。Steadiwear防振手套有望增强患有原发性震颤的人的功能能力的独立性,并减轻对医疗保健系统支持的需求。这项研究的目的是检查注册护士(RN)对Steadiwear防振手套减少社区医护人员面对面支持的潜力的看法。
    方法:11个RN,在农村社区提供护理方面经验丰富,参加了半结构化访谈,分享了他们在社区实践环境中使用Steadiwear防振手套的观点。在布劳恩和克拉克的指导下进行了主题分析。
    结果:护士描述了该技术的价值,以减少客户对日常生活活动的支持需求(例如,敷料,喂养)和日常生活的独立活动(例如,banking,运输)。
    结论:增强对该技术的访问可能会减少卫生系统对护理和个人护理支持的需求。因此,Steadiwear防振手套还显示出延迟和/或防止需要更密集的支撑和减轻过渡到长期护理设施的需要的潜力。
    BACKGROUND: With the increased integration of technologies in the healthcare sector, it is important to understand the benefits emerging technologies may play to reduce demands on the health care system. The Steadiwear antivibration glove shows promise for enhancing the independence in functional abilities for persons with essential tremors and for alleviating the need for support from the health care system. The objective of this study was to examine Registered Nurses\' (RN) perceptions of the potential for the Steadiwear antivibration glove to reduce the need for in-person support from community healthcare workers.
    METHODS: Eleven RNs, experienced in providing care in rural communities, participated in a semi-structured interview sharing their perspectives towards use of the Steadiwear antivibration glove in community practice settings. Thematic analysis guided by Braun and Clarke was undertaken.
    RESULTS: Nurses described the value of this technology to reduce client needs for support for activities of daily living (e.g., dressing, feeding) and independent activities of daily living (e.g., banking, transportation).
    CONCLUSIONS: Enhanced access to this technology may reduce the need for nursing and personal care support from the health system. Therefore the Steadiwear antivibration glove also shows potential to delay and/or prevent the need for more intensive support and mitigate the need for transition to a long-term care facility.
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  • 文章类型: Journal Article
    本研究旨在评估rTMS治疗PD睡眠障碍的疗效。它包括24名患有睡眠障碍的PD患者。组分配(活动或假的比例为2:1)放置在连续编号的封闭信封中。每位患者都进行了以下评估:MDS-UPDRS,帕金森病睡眠量表(PDSS),贝克抑郁量表(BDI),治疗前和治疗后10天的多导睡眠图(PSG)。每节由10列火车组成,20Hz,每人10秒,在顶叶皮层(双侧)。UPDRS的分数,BDI,和PDSS在活性组显着改善,但在假手术组没有改善。PSG数据显示,睡眠开始和快速眼动(REM)潜伏期(min),REM持续时间,与假手术组相比,活动组rTMS后清醒时间(均为%TST)改善。觉醒的次数,睡眠后觉醒指数,唤醒指数,和周期性腿部运动(PLMs)在活动组均显着减少,但在假手术组没有。在顶皮层上进行10次20HzrTMS可改善PD患者的睡眠质量和PLM。PSG和PDSS的改善与UPDRS和BDI评分的改善相关。
    This study aimed to evaluate the efficacy of rTMS in treating sleep disorders in PD. It included 24 patients with PD who had sleep disorders. Group allocations (active or sham with a ratio of 2:1) were placed in serially numbered closed envelopes. Each patient was evaluated with the following: MDS-UPDRS, Parkinson\'s Disease Sleep Scale (PDSS), Beck Depression Inventory (BDI), and polysomnography (PSG) before and 10 days after the treatment sessions. Each session consisted of 10 trains, 20 Hz, 10 sec for each, over the parietal cortex (bilaterally). Scores of UPDRS, BDI, and PDSS improved significantly in the active group but not in the sham group. The PSG data showed that sleep onset and rapid eye movement (REM) latencies (min), REM duration, and time spent awake (both as %TST) were improved after rTMS in the active group compared with the sham group. The number of awakenings, the wake-after-sleep onset index, the arousal index, and periodic leg movements (PLMs) were all significantly reduced in the active group but not in the sham group. Ten sessions of 20 Hz rTMS over parietal cortexes improved sleep quality and PLMs in patients with PD. The improvement in PSG and PDSS were correlated with improvements in UPDRS and BDI scores.
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  • 文章类型: Clinical Trial Protocol
    背景:帕金森病(PD)患者对压力的影响非常敏感。与压力相关的神经精神症状的患病率很高,和急性压力恶化运动症状。动物研究表明,慢性应激可能加速疾病进展,但是人类缺乏这方面的证据。基于正念的干预(MBI)训练参与者专注于当下,有目的,没有判断。先前的研究表明,MBI可以减轻压力,减少PD中的抑郁和焦虑。我们旨在证明正念认知疗法(MBCT)作为PD神经精神(和运动)症状的非药物治疗策略的有效性。并确定PD中应激和应激减轻的潜在机制。
    方法:在一项前瞻性随机对照试验(RCT)中,我们调查8周的MBCT,与照常护理相比,可以减轻PD患者的焦虑和抑郁症状。我们的目标是包括124名PD患者,经历轻度-中度焦虑和抑郁症状的人,有资格进行磁共振成像(MRI)和天真正念,并且疾病持续时间≤10年。每个参与者都被跟踪12个月。临床和生化评估发生在基线(T0),2个月后(T1),12个月后(T2);MRI评估在T0和T2进行。我们的主要结果是T1时医院焦虑和抑郁量表(HADS)的总分,而在T0,年龄,和性别。除了测试MBCT对PD焦虑和抑郁症状的影响,我们探讨MBCT:(1)是否对运动症状严重程度有影响,(2)影响大脑和生化标志物的压力,(3)导致PD进展的生物标志物发生变化。
    结论:MIND-PD是首批进行1年随访的RCT之一,用于研究MBCT对PD患者焦虑和抑郁症状的影响,并探讨PD应激和应激减轻的可能机制。对这些机制的了解可以为将来的新治疗方法铺平道路。
    背景:ClinicalTrials.gov,NCT05779137。2023年1月12日注册。
    BACKGROUND: People with Parkinson\'s disease (PD) are very sensitive to the effects of stress. The prevalence of stress-related neuropsychiatric symptoms is high, and acute stress worsens motor symptoms. Animal studies suggest that chronic stress may accelerate disease progression, but evidence for this in humans is lacking. Mindfulness-based interventions (MBIs) train participants to focus on the present moment, on purpose and without judgement. Previous studies suggest that MBIs may alleviate stress and reduce depression and anxiety in PD. We aim to demonstrate the efficacy of Mindfulness-Based Cognitive Therapy (MBCT) as a non-pharmacologic treatment strategy for neuropsychiatric (and motor) symptoms in PD, and to identify the mechanisms underlying stress and stress reduction in PD.
    METHODS: In a prospective randomized controlled trial (RCT), we investigate whether 8 weeks of MBCT, as compared to care as usual, can reduce symptoms of anxiety and depression in people with PD. We aim to include 124 PD patients, who experience mild-moderate symptoms of anxiety and depression, are eligible for magnetic resonance imaging (MRI) and naïve to mindfulness, and who have a disease duration ≤ 10 years. Every participant is followed for 12 months. Clinical and biochemical assessments take place at baseline (T0), after 2 months (T1), and after 12 months (T2); MRI assessments take place at T0 and T2. Our primary outcome is the total score on the Hospital Anxiety and Depression Scale (HADS) at T1, while correcting for the HADS score at T0, age, and gender. Beyond testing the effects of MBCT on symptoms of anxiety and depression in PD, we explore whether MBCT: (1) has an effect on motor symptom severity, (2) influences cerebral and biochemical markers of stress, and (3) leads to a change in biomarkers of PD progression.
    CONCLUSIONS: MIND-PD is one of the first RCTs with a 1-year follow-up to investigate the effects of MBCT on symptoms of anxiety and depression in PD, and to explore possible mechanisms underlying stress and stress reduction in PD. Insight into these mechanisms can pave the way to new treatment methods in the future.
    BACKGROUND: ClinicalTrials.gov, NCT05779137. Registered on 12 January 2023.
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  • 文章类型: Journal Article
    背景:帕金森病(APD)的晚期诊断对于普通神经科医生来说是一个挑战。已经验证了5-2-1标准和阿万扎达帕金森氏症(CDEPA)的筛查APD。
    目的:本文报告了由运动障碍专家定义的APD的经期患病率,5-2-1标准,和CDEPA,并提高5-2-1标准的筛选性能方法:在曼谷三级医院的帕金森病(PD)诊所进行的横断面回顾性研究,在所有年龄≥18岁的PD患者中,泰国是从2016年1月至2020年1月进行的。我们比较了APD和非APD患者的特点。我们外部验证了5-2-1标准和CDEPA。我们探索了改进5-2-1标准。
    结果:在480名具有完整数据的PD患者中,运动障碍专家对APD的经期患病率,5-2-1标准和CDEPA为37.1%,48.5%,以及27.5%,分别。在原始5-2-1标准的基础上增加了日常生活活动和步态冻结方面的帮助,使敏感性从86.5%(95CI80.6,91.2)提高到94.9%(95CI90.6,97.7),阴性预测值(NPV)从90.3%(95CI85.9,93.7)提高到96%(95CI92.6,98.2)。然而,CDEPA的敏感性为62.9%(95CI55.4,70),NPV为81.0(95CI76.5,85).
    结论:5-2-1标准对于一般神经科医师推荐APD患者进行最佳治疗具有良好的筛选工具性能。修改后的5-2-1标准比原始标准具有更好的性能。需要外部验证。
    BACKGROUND: Advanced stage of Parkinson\'s disease (APD) diagnosis is challenging for general neurologists. The 5-2-1 Criteria and the Cuestionario De Enfermedad de Parkinson Avanzada (CDEPA) have been validated for screening for APD.
    OBJECTIVE: This article reports the period-prevalence of APD defined by a movement disorder expert, the 5-2-1 Criteria, and CDEPA and to improve the screening performance of the 5-2-1 Criteria METHODS: A cross-sectional retrospective study at the Parkinson\'s disease (PD) clinic of a tertiary hospital in Bangkok, Thailand amongst all PD patients aged ≥ 18 years was performed from January 2016 to January 2020. We compared the characteristics of APD and non-APD patients. We externally validated the 5-2-1 Criteria and CDEPA. We explored improving the 5-2-1 Criteria.
    RESULTS: Of 480 PD patients with complete data, the period-prevalence of APD by the movement disorder expert, the 5-2-1 Criteria and CDEPA were 37.1 %, 48.5 %, and 27.5 %, respectively. Adding requiring help with an activity of daily living and freezing of gait to the original 5-2-1 Criteria enhanced the sensitivity from 86.5 % (95 %CI 80.6, 91.2) to 94.9 % (95 %CI 90.6, 97.7) and negative predictive value (NPV) from 90.3 % (95 %CI 85.9, 93.7) to 96 % (95 %CI 92.6, 98.2). However, the CDEPA had a sensitivity of 62.9 % (95 %CI 55.4, 70) and NPV of 81.0 (95 %CI 76.5, 85).
    CONCLUSIONS: The 5-2-1 Criteria had a good screening tool performance for general neurologists to refer APD patients for optimal treatments. The modified 5-2-1 Criteria had better performance than the original one. External validation is needed.
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  • 文章类型: Journal Article
    背景:跑步机步态训练已被证明可以改善帕金森病(PwPD)患者的步态表现,结合虚拟现实,它可以是步态康复的有效工具。游戏化元素的添加可以创建更刺激和粘附的干预。然而,在医疗保健中实施新技术可能具有挑战性。本研究旨在开发和评估PwPD游戏化虚拟现实环境(GVRE)中跑步机康复计划的可行性。
    方法:GVRE是按照以用户为中心的设计方法开发的,让PwPD和物理治疗师参与干预措施的制定和评估。干预包括在三种不同环境中的步行模拟(农村,城市,andpark),难度逐渐增加。为了测试它的可行性,与四名PwPD和四名物理治疗师进行了三次会议。为了评估可用性,系统可用性量表(SUS),使用神经疾病患者辅助技术可用性问卷(NATUQuest)和模拟器疾病问卷(SSQ)。为了评估干预措施的可接受性,收集参与者的反馈和游戏中的表现。
    结果:结果显示干预的可行性,SUS得分为74.82±12.62,NATUQuest得分为4.49±0.62,接受反馈为阳性。参与者对自然主义环境表现出明确的偏好,游戏化元素被认为是积极的。难度设置按预期工作,但在某些情况下降低了体验的乐趣。
    结论:该干预措施被成功证明是在双任务条件下训练PwPD步态的可行选择。它提供了一个安全且可复制的环境,可以在其中训练复杂的情况。然而,干预的进一步迭代需要改进,以保证准确的跟踪和更现实的训练进展。
    背景:NCT05243394-01/20/2022。
    BACKGROUND: Treadmill gait training has been shown to improve gait performance in People with Parkinson\'s Disease (PwPD), and in combination with Virtual Reality, it can be an effective tool for gait rehabilitation. The addition of gamification elements can create a more stimulating and adherent intervention. However, implementation of new technologies in healthcare can be challenging. This study aimed to develop and evaluate the feasibility of a treadmill rehabilitation program in a Gamified Virtual Reality Environment (GVRE) for PwPD.
    METHODS: The GVRE was developed following a user-centered design approach, involving both PwPD and physiotherapists in the development and evaluation of the intervention. The intervention consisted of a walking simulation in three different environments (countryside, city, and park), which had a progressive increase in difficulty. To test its feasibility, three sessions were carried out with four PwPD and four physiotherapists. To assess the usability, the System Usability Scale (SUS), Assistive Technology Usability Questionnaire for people with Neurological diseases (NATU Quest) and Simulator Sickness Questionnaire (SSQ) were used. To assess the intervention\'s acceptability, feedback and in-game performance was collected from participants.
    RESULTS: Results showed the feasibility of the intervention, with a SUS score of 74.82 ± 12.62, and a NATU Quest score of 4.49 ± 0.62, and positive acceptability feedback. Participants showed clear preferences for naturalistic environments, and gamification elements were seen as positive. Difficulty settings worked as intended, but lowered enjoyment of the experience in some cases.
    CONCLUSIONS: This intervention was successfully shown as a feasible option for the training of gait under Dual Task conditions for PwPD. It offers a safe and replicable environment in which complex situations can be trained. However, further iterations of the intervention need to be improved in order to guarantee accurate tracking and a more realistic training progression.
    BACKGROUND: NCT05243394-01/20/2022.
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