提示激励系统促进脑卒中偏瘫患者的功能恢复:一项大样本、单盲、随机对照试验

Da-Hong Gao, Yuanfeng Peng, Bin Dong
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引用次数: 0

摘要

背景和目的:针灸和物理康复训练已被证明可以促进脑卒中偏瘫患者的康复。由于各种因素,许多患者无法持续完成康复训练。本研究旨在探讨腕表佩戴与不佩戴康复训练提醒激励系统对脑卒中偏瘫患者运动功能的影响。受试者和方法:本大样本、单盲、随机对照试验将在安徽中医药大学第二附属医院、牛津国际康复基金会有限公司和牛津布鲁克斯大学进行。将200名脑卒中偏瘫患者随机分为试验组和对照组。这两组患者将接受常规药物治疗、针灸和康复训练。试验组患者将佩戴带有提醒激励系统的智能手表,鼓励他们完成一定数量的个性化体育锻炼任务,对照组患者将佩戴没有提醒激励系统的手表。本研究已于2015年6月16日获得中国临床试验注册中心医学伦理委员会批准(批准号:chiecrct - 20150034)。研究方案:1.0。参与者将提供书面知情同意书。结果:本研究的主要结局指标是出院后3周(即治疗6周后)测量的Barthel指数的差异。次要结局指标包括神经功能缺损评分、美国国立卫生研究院卒中量表评分、Rivermead活动能力指数、蒙特利尔认知评估评分、血压、体重、握力、Timed Up and Go测试评分、运动水平、EuroQol五维度问卷评分、治疗前、治疗3周后和出院后3周(治疗6周后)不良事件。在一项初步研究中,60名中风偏瘫患者接受了针灸和激励康复训练。结果显示,脑卒中偏瘫患者接受拮抗肌长针针刺联合肌肉平衡练习后,Barthel指数和Fugl-Meyer评估量表评分较单独接受拮抗肌长针针刺组升高,修正Ashworth量表评分较单独接受拮抗肌长针针刺组降低。结论:我们将开展一项涉及200名卒中患者的研究,以评估卒中偏瘫患者在接受针灸结合康复训练的同时佩戴带有提醒激励系统的智能手表,与接受类似干预但未接受提醒激励系统的患者相比,是否能更好地恢复运动功能。这些实验数据将支持功能性智能设备辅助康复医疗项目的实施。试验注册:本研究于2015年8月8日在中国临床试验注册中心注册(注册号:ChiCTR-IOR- 15007179)。
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A reminder incentive system promotes the functional recovery of stroke patients with hemiplegia: A large-sample, single-blind, randomized controlled trial
Background and objectives: Acupuncture and physical rehabilitation training have been shown to promote recovery in stroke patients with hemiplegia. Many patients are unable to consistently complete rehabilitation training because of a variety of factors. The aim of this study was to investigate the effects of wearing a wrist watch with versus without a rehabilitation training-reminder incentive system on locomotor function in stroke patients with hemiplegia. Participants and methods: This large-sample, single-blind, randomized controlled trial will be performed at the Second Affiliated Hospital of Anhui University of Chinese Medicine, Oxford International Rehabilitation Foundation Limited, and Oxford Brookes University. A total of 200 stroke patients with hemiplegia will be randomly divided into a test group and a control group. The two groups of patients will receive routine medication, acupuncture, and rehabilitation training. Patients in the test group will wear a smart watch with a reminder incentive system that encourages them to complete a set amount of personalized physical exercise tasks, and patients in the control group will wear a watch without a reminder incentive system. This study was approved by the Medical Ethics Committee of the Chinese Clinical Trial Registry on June 16, 2015 (approval No. ChiECRCT-20150034). Study protocol: 1.0. Participants will provide written informed consent. Results: The primary outcome measure of this study is the differences in the Barthel index measured 3 weeks after discharge (i.e., after 6 weeks of treatment). The secondary outcome measures include neurological deficit scores, National Institutes of Health stroke scale score, Rivermead mobility index, Montreal Cognitive Assessment score, blood pressure, body weight, grip strength, Timed Up and Go Test score, exercise level, EuroQol five dimensions questionnaire score, and adverse events before treatment, after 3 weeks of treatment, and 3 weeks after discharge (after 6 weeks of treatment). In a pilot study, 60 stroke patients with hemiplegia received acupuncture and incentive rehabilitation training. The results showed that in stroke patients with hemiplegia who received elongated needle acupuncture at antagonistic muscles combined with muscle balance exercises, Barthel index and Fugl-Meyer Assessment scale scores increased and Modified Ashworth Scale scores decreased compared with those who received elongated needle acupuncture at antagonistic muscles alone. Conclusion: We will perform a study involving 200 stroke patients to evaluate whether stroke patients with hemiplegia who receive acupuncture combined with rehabilitation training while wearing a smart watch with a reminder incentive system exhibit better recovery of locomotor function compared with those who receive similar interventions but are not exposed to a reminder incentive system. These experimental data will support the implementation of functional smart device-assisted rehabilitation medical programs. Trial registration: This study was registered with Chinese Clinical Trial Registry on August 8, 2015 (registration number: ChiCTR-IOR- 15007179).
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