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Smartphone-based self-monitoring in bipolar disorder: evaluation of usability and feasibility of two systems

机译:双相情感障碍中基于智能手机的自我监控:评估两个系统的可用性和可行性

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Background The aims of the present multicenter pilot study were to examine the feasibility and usability of two different smartphone-based monitoring systems (the Pulso system and the Trilogis-Monsenso system) from two IT companies in patients with bipolar disorder, developed and selected to be testes as a part of a European Union funded Pre-Commercial Procurement (the NYMPHA-MD project). Methods Patients with bipolar disorder (ICD-10),?&?18?years of age during a remitted, partial remitted or mild to moderate depressive state (HDRS-17?&?25) from Italy, Spain and Denmark were included. Patients were randomized 1:1 to the use of one of two smartphone-based monitoring systems. The randomization was stratified according to study location (Italy, Spain, Denmark) and all patients were followed for a 4?weeks study period. Usability and feasibility were evaluated using the Computer System Usability Questionnaire, and the Usefulness, Satisfaction, and Ease of use Questionnaire. Results A total of 60 patients aged 18–69?years with bipolar disorder (ICD-10) recruited from Italy, Spain, Denmark were included—59 patients completed the study. In Denmark, the patients evaluated the Trilogis-Monsenso system with a statistically significant higher usability compared with the Pulso system. In Italy and Spain, the patients evaluated no statistically significant difference between the two systems in any of the categories, except for the usefulness category favoring the Trilogis-Monsenso system (z?=?2.68, p?&?0.01). Conclusions Both monitoring systems showed acceptable usability and feasibility. There were differences in patient-based evaluations of the two monitoring systems related to the country of the study. Studies investigating the usability and feasibility during longer follow-up periods could perhaps reveal different findings. Future randomized controlled trials investigating the possible positive and negative effects of smartphone-based monitoring systems are needed.
机译:背景技术本多中心先导研究的目的是检查来自两家IT公司的两种不同的基于智能手机的监控系统(Pulso系统和Trilogis-Monsenso系统)在双相情感障碍患者中的​​可行性和可用性,这些系统已开发并选择用于睾丸是欧盟资助的商业前采购(NYMPHA-MD项目)的一部分。方法包括来自意大利,西班牙和丹麦的双相情感障碍(ICD-10)≥18岁的患者,其缓解,部分缓解或轻度至中度抑郁状态(HDRS-17≤25)。 。将患者以1:1的比例随机分配到两个基于智能手机的监控系统之一。根据研究地点(意大利,西班牙,丹麦)对随机分组进行分层,并对所有患者进行为期4周的研究。使用计算机系统可用性问卷以及有用性,满意度和易用性问卷对可用性和可行性进行了评估。结果包括来自意大利,西班牙,丹麦的60例18-69岁的双相情感障碍(ICD-10)患者,其中59例完成了研究。在丹麦,患者对Trilogis-Monsenso系统的评价与Pulso系统相比在统计学上具有较高的可用性。在意大利和西班牙,患者在任何类别中均未评价两种系统之间的统计学显着性差异,除了有益于Trilogis-Monsenso系统的有用类别(z≥2.68,p≤0.01)。结论两种监测系统均显示出可接受的可用性和可行性。在与研究国家相关的两个监测系统的基于患者的评估中存在差异。研究较长随访期的可用性和可行性的研究可能会揭示不同的发现。需要进行未来的随机对照试验,以调查基于智能手机的监控系统可能产生的正面和负面影响。

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