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Exploring and Predicting HIV Preexposure Prophylaxis Adherence Patterns Among Men Who Have Sex With Men: Randomized Controlled Longitudinal Study of an mHealth Intervention in Western China. 探索和预测男男性行为者的HIV暴露前预防依从性模式:中国西部移动健康干预的随机对照纵向研究
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-12-12 DOI: 10.2196/58920
Bing Lin, Jiayan Li, Jiaxiu Liu, Wei He, Haiying Pan, Xiaoni Zhong

Background: Preexposure prophylaxis (PrEP) is an effective strategy to reduce the risk of HIV infection. However, the efficacy of PrEP is highly dependent on adherence. Meanwhile, adherence changes over time, making it difficult to manage effectively.

Objective: Our study aimed to explore and predict the patterns of change in PrEP adherence among men who have sex with men (MSM) and evaluate the impact of the WeChat-based reminder intervention on adherence, thus providing more information for PrEP implementation strategies.

Methods: From November 2019 to June 2023, in a randomized controlled longitudinal study of the PrEP demonstration project in Western China (Chongqing, Sichuan, and Xinjiang) based on a mobile health (mHealth) reminder intervention, participants were randomly divided into reminder and no-reminder groups, with those in the reminder group receiving daily reminders based on the WeChat app. Participants were followed up and self-reported their medication adherence every 12 weeks for a total of 5 follow-up visits. We used the growth mixture model (GMM) to explore potential categories and longitudinal trajectories of adherence among MSM, and patterns of change in PrEP adherence were predicted and evaluated based on the decision tree.

Results: A total of 446 MSM were included in the analysis. The GMM identified 3 trajectories of adherence: intermediate adherence group (n=34, 7.62%), low adherence ascending group (n=126, 28.25%), and high adherence decline group (n=286, 64.13%). We included 8 variables that were significant in the univariate analysis in the decision tree prediction model. We found 4 factors and 8 prediction rules, and the results showed that HIV knowledge score, education attainment, mHealth intervention, and HIV testing were key nodes in the patterns of change in adherence. After 10-fold cross-validation, the final prediction model had an accuracy of 75%, and the classification accuracy of low and intermediate adherence was 78.12%.

Conclusions: The WeChat-based reminder intervention was beneficial for adherence. A short set of questions and prediction rules, which can be applied in future large-scale validation studies, aimed at developing and validating a short adherence assessment tool and implementing it in PrEP practices among MSM.

背景:暴露前预防(PrEP)是降低HIV感染风险的有效策略。然而,PrEP的疗效高度依赖于依从性。与此同时,依从性随着时间的推移而变化,这使得有效管理变得困难。目的:本研究旨在探讨和预测男男性行为者(MSM) PrEP依从性的变化规律,并评估微信提醒干预对PrEP依从性的影响,为PrEP实施策略提供更多信息。方法:2019年11月至2023年6月,在中国西部(重庆、四川、新疆)基于移动健康(mHealth)提醒干预的PrEP示范项目随机对照纵向研究中,将参与者随机分为提醒组和无提醒组。提醒组的人每天都会收到基于微信应用程序的提醒。参与者每12周接受一次随访,并自我报告他们的药物依从性,总共进行了5次随访。我们使用生长混合模型(GMM)来探索MSM的潜在类别和依从性的纵向轨迹,并基于决策树预测和评估PrEP依从性的变化模式。结果:共纳入446例男男性行为者。GMM鉴定出3种依附性轨迹:中等依附性组(n=34, 7.62%)、低依附性上升组(n=126, 28.25%)和高依附性下降组(n=286, 64.13%)。我们在决策树预测模型中纳入了8个在单变量分析中显著的变量。结果表明,HIV知识得分、受教育程度、移动健康干预和HIV检测是影响依从性变化模式的关键节点。经10倍交叉验证,最终预测模型准确率为75%,低、中依从性分类准确率为78.12%。结论:基于微信的提醒干预有利于依从性。一套简短的问题和预测规则,可应用于未来的大规模验证研究,旨在开发和验证一种简短的依从性评估工具,并在男男性接触者的PrEP实践中实施。
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引用次数: 0
An Ecological Momentary Assessment Approach of Environmental Triggers in the Role of Daily Affect, Rumination, and Movement Patterns in Early Alcohol Use Among Healthy Adolescents: Exploratory Study. 环境触发因素在健康青少年早期饮酒中的日常情绪、反刍和运动模式作用的生态瞬间评估方法:探索性研究
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-12-10 DOI: 10.2196/53401
Maren Prignitz, Stella Guldner, Stephan Johann Lehmler, Pascal-M Aggensteiner, Frauke Nees

Background: Adolescence is a period characterized by an increased susceptibility to developing risky alcohol consumption habits. This susceptibility can be influenced by social and situational factors encountered in daily life, which, in conjunction with emotions and thoughts, contribute to behavioral patterns related to alcohol use even in the early stages of alcohol experimentation, when initial experiences with alcohol are formed, and regular consumption is still evolving.

Objective: This study aimed to examine the association between detailed behavioral and movement patterns, along with emotional and cognitive factors, and the early onset of alcohol use in the everyday lives of adolescents.

Methods: A total of 65 healthy adolescents (33 male, twenty-nine 14-year-olds, and thirty-six 16-year-olds) underwent mobile-based ecological momentary assessments on alcohol (once a day at 9 AM, assessing alcohol use the day before), positive and negative affect, craving, rumination, and social context (6 prompts/day at 9 AM, 11 AM, 2 PM, 4 PM, 6 PM and 8 PM), type of day (weekdays or weekends, with weekend including Fridays, Saturdays, and Sundays), and using geospatial measures (specifically roaming entropy and number and type of trigger points for alcohol use met) over 14 days. After adjusting for a compliance rate of at least 50%, 52 participants (26 male and twenty-four 14-year-olds) were included in the analyses.

Results: Generalized linear multilevel models revealed that higher positive affect (b=0.685, P=.007), higher rumination (b=0.586, P=.02), and a larger movement radius (roaming entropy) (b=8.126, P=.02) were positively associated with alcohol use on the same day. However, social context (b=-0.076, P=.90), negative affect (b=-0.077, P=.80), or potential trigger points (all P>.05) did not show significant associations. Alcohol use varied depending on the type of day, with more alcohol use on weekends (b=1.082, P<.001) and age (t50=-2.910, P=.005), with 16-year-olds (mean 1.61, SD 1.66) reporting more days of alcohol consumption than 14-year-olds (mean 0.548, SD 0.72).

Conclusions: Our findings support previously identified factors as significant contributors to very early and low levels of alcohol consumption through fine-grained analysis of daily behaviors. These factors include positive affect, rumination, weekend days, and age. In addition, we emphasize that exploratory environmental movement behavior (roaming entropy) is also significantly associated with adolescent alcohol use, highlighting its importance as an additional factor.

背景:青春期是一个容易养成危险饮酒习惯的时期。这种易感性可能会受到日常生活中遇到的社会和情景因素的影响,这些因素与情绪和思想相结合,甚至在尝试饮酒的早期阶段,就会促成与饮酒有关的行为模式,因为此时对酒精的初步体验已经形成,而定期饮酒仍在发展之中:本研究旨在探讨青少年日常生活中的详细行为和动作模式,以及情绪和认知因素与早期饮酒之间的关联:共有 65 名健康青少年(33 名男性、29 名 14 岁青少年和 36 名 16 岁青少年)接受了基于手机的生态瞬间评估,评估内容包括酒精(每天上午 9 点进行一次,评估前一天的酒精使用情况)、积极和消极情绪、渴望、反刍和社会环境(6 次提示/次/天)、和社会环境(每天 6 次提示,分别在上午 9 点、上午 11 点、下午 2 点、下午 4 点、下午 6 点和晚上 8 点)、日期类型(工作日或周末,周末包括周五、周六和周日),并在 14 天内使用地理空间测量(特别是漫游熵和满足酒精使用触发点的数量和类型)。在对至少 50%的遵从率进行调整后,52 名参与者(26 名男性和 24 名 14 岁青少年)被纳入分析范围:广义线性多层次模型显示,较高的积极情绪(b=0.685,P=.007)、较高的反刍(b=0.586,P=.02)和较大的运动半径(漫游熵)(b=8.126,P=.02)与当日饮酒呈正相关。然而,社会环境(b=-0.076,P=.90)、负面情绪(b=-0.077,P=.80)或潜在触发点(均大于 P.05)并没有显示出显著的关联。饮酒量因日期而异,周末饮酒量更大(b=1.082,P50=-2.910,P=.005),16 岁儿童(平均 1.61,标准差 1.66)的饮酒天数多于 14 岁儿童(平均 0.548,标准差 0.72):我们的研究结果支持之前通过对日常行为进行精细分析而确定的导致过早饮酒和低水平饮酒的重要因素。这些因素包括积极情绪、反刍、周末日和年龄。此外,我们还强调,探索性的环境运动行为(漫游熵)也与青少年饮酒有显著关联,突出了其作为额外因素的重要性。
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引用次数: 0
Feasibility and Efficacy of a Novel Mindfulness App Used With Matcha Green Tea in Generally Healthy Adults: Randomized Controlled Trial. 新型正念应用程序与抹茶绿茶一起用于一般健康成年人的可行性和有效性:随机对照试验
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-12-10 DOI: 10.2196/63078
Ryohei Tanaka-Kanegae, Koji Yamada, Chad M Cook, Traci M Blonquist, Kristen D Taggart, Koichiro Hamada
<p><strong>Background: </strong>Mindfulness practices, such as breathing meditation (BM), reduce stress and enhance mood. One such practice is mindful eating, where a practitioner focuses on the five senses while eating or drinking. A novel set of prototypes has been developed, incorporating principles of mindful eating. These prototypes include matcha green tea and a mobile app that provides audio guidance for meditation during the preparation and consumption of the beverage (hereafter referred to as guided tea meditation [GTM]).</p><p><strong>Objective: </strong>This study assessed the feasibility and efficacy of GTM, evaluating meditation time, frequency, and prototype acceptability over 8 weeks, alongside changes in stress and mood. Additionally, other benefits of GTM were explored.</p><p><strong>Methods: </strong>A comparator group was established in which participants performed traditional BM without an app or audio guide (active control). This unblinded randomized controlled trial involved 100 healthy American volunteers (n=49 GTM, n=51 BM). During the 8-week study period, participants were encouraged to perform either GTM or BM for 10 minutes daily. The meditation activity was self-reported the following day. Only the GTM group assessed the prototype acceptability. The Perceived Stress Scale-10 was used to measure stress levels, while the Two-Dimensional Mood Scale was used to evaluate mood changes. Other meditation benefits were explored using a questionnaire. All questionnaires were presented and completed via an app. An intention-to-treat analysis was performed.</p><p><strong>Results: </strong>No significant between-group differences were found in total meditation time (P=.15) or frequency (P=.36). However, the weekly time and frequency of the GTM group remained above 50 minutes per week and 4 days per week, respectively. Over half of the GTM participants (≥28/49, ≥57%) accepted the prototype. The GTM group exhibited significant stress reductions at weeks 4 and 8 (both P<.001), similar to the BM group. Improvements in mood metrics were observed after a single GTM session on days 1 and 56, similar to the BM group. Moreover, increases in premeditation scores for relaxed and calm from day 1 to day 56 were significantly higher for the GTM group (P=.04 and .048, respectively). The majority of participants (≥25/49, ≥51%) assigned to GTM experienced positive changes in happiness, time management, quality of life, relationships, sleep, and work performance as they continued meditating. However, no significant between-group differences were found in these exploratory outcomes (P>.08).</p><p><strong>Conclusions: </strong>We believe that GTM exhibits good feasibility. Meanwhile, GTM reduced stress, improved mood, and let the practitioners feel other benefits, similar to BM. Long-term practitioners of GTM may even feel more relaxed and calmer in the state of premeditation than those who practice BM.</p><p><strong>Trial registration: </strong>Clini
背景介绍正念练习,如呼吸冥想(BM),可以减轻压力,改善情绪。正念进食就是这样一种练习,练习者在进食或饮水时专注于五感。结合正念饮食的原则,我们开发了一套新颖的原型。这些原型包括抹茶绿茶和一款移动应用程序,该应用程序可在准备和饮用饮料的过程中提供冥想音频指导(以下简称为导茶冥想[GTM]):本研究评估了 GTM 的可行性和有效性,评估了 8 周内冥想的时间、频率和原型的可接受性,以及压力和情绪的变化。此外,还探讨了 GTM 的其他益处:设立了一个比较组,让参与者在没有应用程序或音频指导的情况下进行传统的 BM(主动对照组)。这项非盲法随机对照试验涉及 100 名健康的美国志愿者(GTM 49 人,BM 51 人)。在为期 8 周的研究期间,鼓励参与者每天进行 10 分钟的 GTM 或 BM。冥想活动在第二天进行自我报告。只有 GTM 组评估了原型的可接受性。感知压力量表-10 用于测量压力水平,二维情绪量表用于评估情绪变化。其他冥想益处则通过问卷进行了探讨。所有问卷均通过一款应用程序进行展示和填写。进行了意向治疗分析:在冥想总时间(P=.15)或频率(P=.36)方面,没有发现明显的组间差异。然而,GTM 组的每周冥想时间和频率分别保持在 50 分钟和每周 4 天以上。超过一半的 GTM 参与者(≥28/49,≥57%)接受了原型。在第 4 周和第 8 周,GTM 组的压力明显减轻(均为 P.08):我们认为 GTM 具有良好的可行性。同时,GTM 还能减轻压力、改善情绪,并让练习者感受到与 BM 相似的其他益处。长期练习 GTM 的人甚至会比练习 BM 的人在预想状态下感觉更放松、更平静:ClinicalTrials.gov NCT05832645; https://clinicaltrials.gov/study/NCT05832645.
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引用次数: 0
Functions of Smartphone Apps and Wearable Devices Promoting Physical Activity: Six-Month Longitudinal Study on Japanese-Speaking Adults. 智能手机应用和可穿戴设备促进身体活动的功能:对日语成年人为期6个月的纵向研究。
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-12-10 DOI: 10.2196/59708
Naoki Konishi, Takeyuki Oba, Keisuke Takano, Kentaro Katahira, Kenta Kimura
<p><strong>Background: </strong>Smartphone apps and wearable activity trackers are increasingly recognized for their potential to promote physical activity (PA). While studies suggest that the use of commercial mobile health tools is associated with higher PA levels, most existing evidence is cross-sectional, leaving a gap in longitudinal data.</p><p><strong>Objective: </strong>This study aims to identify app-use patterns that are prospectively associated with increases in and maintenance of PA. The primary objective was to test whether continued app use is linked to adherence to the recommended PA levels (ie, 23 metabolic equivalent task [MET] hours per week for adults or 10 MET hours/week for individuals aged >65 years) during a follow-up assessment. The secondary objective was to explore which functions and features of PA apps predict changes in PA levels.</p><p><strong>Methods: </strong>A 2-wave longitudinal survey was conducted, with baseline and follow-up assessments separated by 6 months. A total of 20,573 Japanese-speaking online respondents participated in the baseline survey, and 16,286 (8289 women; mean age 54.7 years, SD 16.8 years) completed the follow-up. At both time points, participants reported their current PA levels and whether they were using any PA apps or wearables. Each participant was classified into 1 of the following 4 categories: continued users (those using apps at both the baseline and follow-up; n=2150, 13.20%), new users (those who started using apps before the follow-up; n=1462, 8.98%), discontinued users (those who had used apps at baseline but not at follow-up; n=1899, 11.66%), and continued nonusers (those who had never used apps; n=10,775, 66.16%).</p><p><strong>Results: </strong>The majority of continued users (1538/2150, 71.53%) either improved or maintained their PA at the recommended levels over 6 months. By contrast, discontinued users experienced the largest reduction in PA (-7.95 MET hours/week on average), with more than half failing to meet the recommended levels at the follow-up (n=968, 50.97%). Analyses of individual app functions revealed that both energy analysis (eg, app calculation of daily energy expenditure) and journaling (eg, users manually entering notes and maintaining an exercise diary) were significantly associated with increases in PA. Specifically, energy analysis was associated with an odds ratio (OR) of 1.67 (95% CI 1.05-2.64, P=.03), and journaling had an OR of 1.76 (95% CI 1.12-2.76, P=.01). By contrast, individuals who maintained the recommended PA levels at the follow-up were more likely to use the goal setting (OR 1.73, 95% CI 1.21-2.48, P=.003), sleep information (OR 1.66, 95% CI 1.03-2.68, P=.04), and blood pressure recording (OR 2.05, 95% CI 1.10-3.83, P=.02) functions.</p><p><strong>Conclusions: </strong>The results highlight the importance of continued app use in both increasing and maintaining PA levels. Different app functions may contribute to these outcomes, with feature
背景:智能手机应用程序和可穿戴活动追踪器因其促进身体活动(PA)的潜力而越来越受到认可。虽然研究表明,商业移动医疗工具的使用与较高的PA水平有关,但大多数现有证据是横断面的,在纵向数据上留下了空白。目的:本研究旨在确定应用程序使用模式与PA的增加和维持可能相关。主要目的是在随访评估中测试持续使用应用程序是否与坚持推荐的PA水平(即成人每周23代谢当量任务[MET]小时或年龄在50至65岁之间的个体每周10 MET小时)有关。第二个目标是探索PA应用程序的哪些功能和特性可以预测PA水平的变化。方法:采用2波纵向调查,基线与随访间隔6个月。共有20,573名说日语的在线受访者参与了基线调查,16,286人(8289名女性;平均年龄54.7岁,SD 16.8岁)完成随访。在这两个时间点,参与者报告了他们目前的PA水平,以及他们是否使用任何PA应用程序或可穿戴设备。每个参与者被分为以下4类中的1类:持续用户(在基线和随访期间都使用应用程序的用户;N =2150, 13.20%),新用户(在随访前开始使用应用程序的用户;N =1462, 8.98%),停用用户(在基线时使用应用程序,但在随访时未使用;N =1899, 11.66%),以及持续的非用户(从未使用过应用程序的人;66.16%, n = 10775)。结果:大多数持续使用者(1538/2150,71.53%)在6个月内改善或维持其PA在推荐水平。相比之下,停用药物的患者PA下降幅度最大(平均每周-7.95 MET小时),超过一半的患者在随访时未能达到推荐水平(n=968, 50.97%)。对单个应用程序功能的分析显示,能量分析(例如,应用程序计算每日能量消耗)和日志记录(例如,用户手动输入笔记并保持锻炼日记)都与PA的增加显著相关。具体来说,能量分析的比值比(OR)为1.67 (95% CI 1.05-2.64, P= 0.03),记录的比值比(OR)为1.76 (95% CI 1.12-2.76, P= 0.01)。相比之下,在随访中保持推荐的PA水平的个体更有可能使用目标设定(OR 1.73, 95% CI 1.21-2.48, P= 0.003)、睡眠信息(OR 1.66, 95% CI 1.03-2.68, P= 0.04)和血压记录(OR 2.05, 95% CI 1.10-3.83, P= 0.02)功能。结论:结果强调了持续使用app对增加和维持PA水平的重要性。不同的应用功能可能对这些结果有影响,目标设定和日志等功能在增加PA方面发挥着关键作用,而与整体健康相关的功能,如睡眠跟踪和血压监测,与保持高PA水平更相关。
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引用次数: 0
Influencing Factors and Implementation Pathways of Adherence Behavior in Intelligent Personalized Exercise Prescription: Qualitative Study. 智能个性化运动处方依从性行为的影响因素及实施途径:定性研究。
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-12-05 DOI: 10.2196/59610
Xuejie Xu, Guoli Zhang, Yuxin Xia, Hui Xie, Zenghui Ding, Hongyu Wang, Zuchang Ma, Ting Sun
<p><strong>Background: </strong>Personalized intelligent exercise prescriptions have demonstrated significant benefits in increasing physical activity and improving individual health. However, the health benefits of these prescriptions depend on long-term adherence. Therefore, it is essential to analyze the factors influencing adherence to personalized intelligent exercise prescriptions and explore the intrinsic relationship between individual behavioral motivation and adherence. This understanding can help improve adherence and maximize the effectiveness of such prescriptions.</p><p><strong>Objective: </strong>This study aims to identify the factors influencing adherence behavior among middle-aged and older community residents who have been prescribed personalized exercise regimens through an electronic health promotion system. It also explores how these factors affect the initiation and maintenance of adherence behavior.</p><p><strong>Methods: </strong>We used purposive sampling to conduct individual, face-to-face semistructured interviews based on the Transtheoretical Model (TTM) with 12 middle-aged and older community residents who had been following personalized exercise regimens for 8 months. These residents had received detailed exercise health education and guidance from staff. The interviews were recorded, transcribed verbatim, and analyzed using NVivo software through grounded theory. We then applied the TTM and multibehavioral motivation theory to analyze the factors influencing adherence. Additionally, the relationship between behavioral motivations and adherence was explored.</p><p><strong>Results: </strong>Using the behavior change stages of the TTM, open coding yielded 21 initial categories, which were then organized into 8 main categories through axial coding: intrinsic motivation, extrinsic motivation, benefit motivation, pleasure motivation, achievement motivation, perceived barriers, self-regulation, and optimization strategies. Selective coding further condensed these 8 main categories into 3 core categories: "multitheory motivation," "obstacle factors," and "solution strategies." Using the coding results, a 3-level model of factors influencing adherence to intelligent personalized exercise prescriptions was developed. Based on this, an implementation path for promoting adherence to intelligent personalized exercise prescriptions was proposed by integrating the model with the TTM.</p><p><strong>Conclusions: </strong>Adherence to personalized exercise prescriptions is influenced by both facilitating factors (eg, multibehavioral motivation, optimization strategies) and obstructive factors (eg, perceived barriers). Achieving and maintaining adherence is a gradual process, shaped by a range of motivations and factors. Personalized solutions, long-term support, feedback mechanisms, and social support networks are essential for promoting adherence. Future efforts should focus on enhancing adherence by strengthening multibehavioral m
背景:个性化智能运动处方在增加身体活动和改善个人健康方面已经证明了显著的益处。然而,这些处方的健康效益取决于长期坚持。因此,分析个性化智能运动处方依从性的影响因素,探索个体行为动机与依从性之间的内在关系是十分必要的。这种理解可以帮助提高依从性,并最大限度地提高这些处方的有效性。目的:本研究旨在通过电子健康促进系统了解社区中老年居民个体化运动方案的依从性影响因素。它还探讨了这些因素如何影响依从性行为的开始和维持。方法:采用有目的抽样的方法,基于跨理论模型(Transtheoretical Model, TTM)对12名遵循个性化运动方案8个月的社区中老年居民进行面对面的半结构化访谈。这些住院病人接受了详细的运动健康教育和工作人员的指导。访谈记录,逐字转录,并通过接地理论使用NVivo软件进行分析。然后,我们运用TTM和多行为动机理论分析了影响依从性的因素。此外,还探讨了行为动机与依从性之间的关系。结果:利用TTM的行为改变阶段,开放编码得到21个初始类别,然后通过轴向编码将其分为8个主要类别:内在动机、外在动机、利益动机、愉悦动机、成就动机、感知障碍、自我调节和优化策略。选择性编码进一步将这8个主要类别浓缩为3个核心类别:“多理论动机”、“障碍因素”和“解决策略”。利用编码结果,建立了影响智能个性化运动处方依从性因素的三层次模型。在此基础上,提出了将模型与TTM相结合,促进智能个性化运动处方依从性的实施路径。结论:个性化运动处方的依从性受到促进因素(如多行为动机、优化策略)和阻碍因素(如感知障碍)的双重影响。实现和保持坚持是一个渐进的过程,受到一系列动机和因素的影响。个性化解决方案、长期支持、反馈机制和社会支持网络对于促进依从性至关重要。未来的工作应侧重于通过加强多行为动机、优化解决方案和解决障碍来提高整体依从性。
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引用次数: 0
The Role of Smartwatch Technology in the Provision of Care for Type 1 or 2 Diabetes Mellitus or Gestational Diabetes: Systematic Review. 智能手表技术在1型或2型糖尿病或妊娠糖尿病护理中的作用:系统综述。
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-12-03 DOI: 10.2196/54826
Sergio Diez Alvarez, Antoni Fellas, Katie Wynne, Derek Santos, Dean Sculley, Shamasunder Acharya, Pooshan Navathe, Xavier Gironès, Andrea Coda
<p><strong>Background: </strong>The use of smart technology in the management of all forms of diabetes mellitus has grown significantly in the past 10 years. Technologies such as the smartwatch have been proposed as a method of assisting in the monitoring of blood glucose levels as well as other alert prompts such as medication adherence and daily physical activity targets. These important outcomes reach across all forms of diabetes and have the potential to increase compliance of self-monitoring with the aim of improving long-term outcomes such as hemoglobin A1c (HbA1c).</p><p><strong>Objective: </strong>This systematic review aims to explore the literature for evidence of smartwatch technology in type 1, 2, and gestational diabetes.</p><p><strong>Methods: </strong>A systematic review was undertaken by searching Ovid MEDLINE and CINAHL databases. A second search using all identified keywords and index terms was performed on Ovid MEDLINE (January 1966 to August 2023), Embase (January 1980 to August 2023), Cochrane Central Register of Controlled Trials (CENTRAL, the Cochrane Library, latest issue), CINAHL (from 1982), IEEE Xplore, ACM Digital Libraries, and Web of Science databases. Type 1, type 2, and gestational diabetes were eligible for inclusion. Quantitative studies such as prospective cohort or randomized clinical trials that explored the feasibility, usability, or effect of smartwatch technology in people with diabetes were eligible. Outcomes of interest were changes in blood glucose or HbA1c, physical activity levels, medication adherence, and feasibility or usability scores.</p><p><strong>Results: </strong>Of the 8558 titles and abstracts screened, 5 studies were included for qualitative synthesis in this review. A total of 322 participants with either type 1 or type 2 diabetes mellitus were included in the review. A total of 4 studies focused on the feasibility and usability of smartwatch technology in diabetes management. One study conducted a proof-of-concept randomized clinical trial including smartwatch technology for exercise time prescriptions for participants with type 2 diabetes mellitus. Adherence of participants to smartwatch technology varied between included studies, with one reporting input submissions of 58% and another reporting that participants logged 50% more entries than they were required to. One study reported significantly improved glycemic control with integrated smartwatch technology, with increased exercise prescriptions; however, this study was not powered and required a longer observational period.</p><p><strong>Conclusions: </strong>This systematic review has highlighted the lack of robust randomized clinical trials that explore the efficacy of smartwatch technology in the management of patients with type 1, type 2, and gestational diabetes. Further research is required to establish the role of integrated smartwatch technology in important outcomes such as glycemic control, exercise participation, drug adhere
背景:在过去10年中,智能技术在各种形式糖尿病管理中的应用显著增长。像智能手表这样的技术已经被提议作为一种帮助监测血糖水平的方法,以及其他警报提示,如药物依从性和日常体育活动目标。这些重要的结果适用于所有形式的糖尿病,并有可能增加自我监测的依从性,以改善血红蛋白A1c (HbA1c)等长期结果。目的:本系统综述旨在探讨智能手表技术在1型、2型和妊娠期糖尿病中的应用。方法:检索Ovid MEDLINE和CINAHL数据库进行系统评价。在Ovid MEDLINE(1966年1月至2023年8月)、Embase(1980年1月至2023年8月)、Cochrane Central Register of Controlled Trials (Central, Cochrane Library,最新一期)、CINAHL(1982年起)、IEEE Xplore、ACM数字图书馆和Web of Science数据库中使用所有确定的关键词和索引项进行第二次搜索。1型、2型和妊娠期糖尿病符合纳入条件。定量研究,如前瞻性队列或随机临床试验,探索智能手表技术在糖尿病患者中的可行性、可用性或效果是合格的。感兴趣的结果是血糖或糖化血红蛋白的变化、身体活动水平、药物依从性以及可行性或可用性评分。结果:在筛选出的8558篇标题和摘要中,有5篇研究被纳入本综述的定性综合。共有322名1型或2型糖尿病患者被纳入本综述。共有4项研究关注智能手表技术在糖尿病管理中的可行性和可用性。一项研究进行了一项概念验证的随机临床试验,其中包括为2型糖尿病患者提供运动时间处方的智能手表技术。在被纳入的研究中,参与者对智能手表技术的依从性各不相同,一项研究报告的输入提交率为58%,另一项研究报告的输入量比要求的多50%。一项研究报告称,集成智能手表技术显著改善了血糖控制,增加了运动处方;然而,这项研究没有动力,需要更长的观察期。结论:本系统综述强调了缺乏可靠的随机临床试验来探索智能手表技术在1型、2型和妊娠糖尿病患者管理中的疗效。需要进一步的研究来确定集成智能手表技术在各种糖尿病患者的血糖控制、运动参与、药物依从性和饮食监测等重要结果中的作用。
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引用次数: 0
Personalized Smartphone-Enabled Assessment of Blood Pressure and Its Treatment During the SARS-CoV-2 COVID-19 Pandemic in Patients From the CURE-19 Study: Longitudinal Observational Study. 来自CURE-19研究的患者在SARS-CoV-2 COVID-19大流行期间的个性化智能手机血压评估及其治疗:纵向观察研究
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-12-03 DOI: 10.2196/53430
Leanne Richardson, Nihal Noori, Jack Fantham, Gregor Timlin, James Siddle, Thomas Godec, Mike Taylor, Charles Baum
<p><strong>Background: </strong>The use of digital interventions by patients for remote monitoring and management of health and disease is increasing. This observational study examined the feasibility, use, and safety of a digital smartphone app for routine monitoring of blood pressure (BP), medication, and symptoms of COVID-19 during the COVID-19 pandemic.</p><p><strong>Objective: </strong>The objective of this study was to deploy and test electronic data recording using a smartphone app developed for routine monitoring of BP in patients with primary hypertension. We tested the app for ease of data entry in BP management and tracking symptoms of new-onset COVID-19 to determine if participants found this app approach useful and sustainable.</p><p><strong>Methods: </strong>This remote, decentralized, 12-week, prospective, observational study was conducted in a community setting within the United States. Participants were approached and recruited from affiliated sites where they were enrolled in an ongoing remote decentralized study (CURE-19) of participants experiencing the COVID-19 pandemic. Potential participants were asked to complete a digital screener to determine eligibility and given informed consent forms to read and consent to using the Curebase digital platform. Following enrollment, participants downloaded the digital app to their smartphones for all data collection. Participants recorded daily BP, associated medication use, and emergent symptoms associated with SARS-CoV-2 infection. In addition, usability (adherence, acceptability, and user experience) was assessed using standard survey questions. Adverse events were collected based on participant self-report. Compliance and engagement were determined from user data entry rates. Feasibility and participant feedback were assessed upon study completion using the User Experience Questionnaire.</p><p><strong>Results: </strong>Of the 389 participants who enrolled in and completed the study, 380 (98%) participants downloaded and entered BP routines in week 1. App engagement remained high; 239 (62.9%) of the 380 participants remained in the study for the full 12-week observation period, and 201 (84.1%) of the 239 participants entered full BP routines into the digital app 80% or more of the time. The smartphone app scored an overall positive evaluation as assessed by the User Experience Questionnaire and was benchmarked as "excellent" for domains of perspicuity, efficiency, and dependability and "above average" for domains of attractiveness and stimulation. Highly adherent participants with hypertension demonstrated well-controlled BP, with no significant changes in average systolic or diastolic BP between week 1 and week 12 (all P>.05). Participants were able to record BP medications and symptoms of SARS-CoV-2 infection. No adverse events attributable to the use of the smartphone app were reported during the observational period.</p><p><strong>Conclusions: </strong>The high retention, engagem
背景:越来越多的患者使用数字干预手段对健康和疾病进行远程监测和管理。本观察性研究探讨了在COVID-19大流行期间用于常规监测血压(BP)、药物和COVID-19症状的数字智能手机应用程序的可行性、使用和安全性。目的:本研究的目的是使用一款智能手机应用程序部署和测试电子数据记录,该应用程序用于原发性高血压患者的血压常规监测。我们测试了该应用程序在血压管理和跟踪新发COVID-19症状方面的数据输入便利性,以确定参与者是否认为该应用程序方法有用且可持续。方法:这项远程、分散、为期12周的前瞻性观察性研究在美国的一个社区环境中进行。研究人员接触并招募了来自附属站点的参与者,他们参加了正在进行的针对正在经历COVID-19大流行的参与者的远程分散研究(CURE-19)。潜在的参与者被要求完成一个数字筛选来确定资格,并给予知情同意书来阅读和同意使用Curebase数字平台。注册后,参与者将数字应用程序下载到他们的智能手机上,以便收集所有数据。参与者记录了每日血压、相关药物使用以及与SARS-CoV-2感染相关的紧急症状。此外,可用性(依从性、可接受性和用户体验)使用标准调查问题进行评估。不良事件收集基于参与者的自我报告。合规性和参与度由用户数据输入率决定。可行性和参与者的反馈在研究完成后使用用户体验问卷进行评估。结果:在389名参加并完成研究的参与者中,380名(98%)参与者在第1周下载并进入BP例行程序。应用粘性仍然很高;380名参与者中有239人(62.9%)在整个12周的观察期中仍在研究中,239名参与者中有201人(84.1%)在80%或更多的时间里在数字应用程序中输入了完整的BP例程。在用户体验问卷中,这款智能手机应用获得了总体积极的评价,在清晰度、效率和可靠性方面被评为“优秀”,在吸引力和刺激方面被评为“中等以上”。高血压患者表现出良好的血压控制,在第1周和第12周之间,平均收缩压和舒张压没有显著变化(均P < 0.05)。参与者能够记录降压药物和SARS-CoV-2感染的症状。在观察期间,没有报告可归因于使用智能手机应用程序的不良事件。结论:本研究的高保留度、参与度、可接受性和积极反馈表明,在社区环境下,使用智能手机应用程序对高血压患者进行血压和药物常规监测是可行的。远程监测血压和数据收集可与高血压药物联合用药(药物+数字),实现高血压的精准管理。
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引用次数: 0
Auxiliary Diagnosis of Children With Attention-Deficit/Hyperactivity Disorder Using Eye-Tracking and Digital Biomarkers: Case-Control Study. 注意力缺陷/多动症儿童的辅助诊断:使用新型数字生物标记的眼动追踪研究。
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-11-29 DOI: 10.2196/58927
Zhongling Liu, Jinkai Li, Yuanyuan Zhang, Dan Wu, Yanyan Huo, Jianxin Yang, Musen Zhang, Chuanfei Dong, Luhui Jiang, Ruohan Sun, Ruoyin Zhou, Fei Li, Xiaodan Yu, Daqian Zhu, Yao Guo, Jinjin Chen

Background: Attention-deficit/hyperactivity disorder (ADHD) is a common neurodevelopmental disorder in school-aged children. The lack of objective biomarkers for ADHD often results in missed diagnoses or misdiagnoses, which lead to inappropriate or delayed interventions. Eye-tracking technology provides an objective method to assess children's neuropsychological behavior.

Objective: The aim of this study was to develop an objective and reliable auxiliary diagnostic system for ADHD using eye-tracking technology. This system would be valuable for screening for ADHD in schools and communities and may help identify objective biomarkers for the clinical diagnosis of ADHD.

Methods: We conducted a case-control study of children with ADHD and typically developing (TD) children. We designed an eye-tracking assessment paradigm based on the core cognitive deficits of ADHD and extracted various digital biomarkers that represented participant behaviors. These biomarkers and developmental patterns were compared between the ADHD and TD groups. Machine learning (ML) was implemented to validate the ability of the extracted eye-tracking biomarkers to predict ADHD. The performance of the ML models was evaluated using 5-fold cross-validation.

Results: We recruited 216 participants, of whom 94 (43.5%) were children with ADHD and 122 (56.5%) were TD children. The ADHD group showed significantly poorer performance (for accuracy and completion time) than the TD group in the prosaccade, antisaccade, and delayed saccade tasks. In addition, there were substantial group differences in digital biomarkers, such as pupil diameter fluctuation, regularity of gaze trajectory, and fixations on unrelated areas. Although the accuracy and task completion speed of the ADHD group increased over time, their eye-movement patterns remained irregular. The TD group with children aged 5 to 6 years outperformed the ADHD group with children aged 9 to 10 years, and this difference remained relatively stable over time, which indicated that the ADHD group followed a unique developmental pattern. The ML model was effective in discriminating the groups, achieving an area under the curve of 0.965 and an accuracy of 0.908.

Conclusions: The eye-tracking biomarkers proposed in this study effectively identified differences in various aspects of eye-movement patterns between the ADHD and TD groups. In addition, the ML model constructed using these digital biomarkers achieved high accuracy and reliability in identifying ADHD. Our system can facilitate early screening for ADHD in schools and communities and provide clinicians with objective biomarkers as a reference.

背景介绍注意力缺陷/多动障碍(ADHD)是学龄儿童常见的神经发育障碍。由于缺乏针对多动症的客观生物标志物,常常导致漏诊或误诊,从而导致干预措施不当或延误。眼动追踪技术为评估儿童的神经心理行为提供了一种客观的方法:本研究旨在利用眼动跟踪技术开发一种客观可靠的多动症辅助诊断系统。该系统对学校和社区的多动症筛查很有价值,并有助于确定临床诊断多动症的客观生物标志物:我们对患有多动症的儿童和发育正常(TD)的儿童进行了一项病例对照研究。我们根据多动症的核心认知缺陷设计了眼动追踪评估范式,并提取了代表参与者行为的各种数字生物标记。我们将这些生物标记和发育模式在多动症组和多动症组之间进行了比较。为了验证提取的眼动生物标记预测多动症的能力,我们采用了机器学习(ML)方法。使用 k 倍交叉验证对 ML 模型的性能进行了评估:我们招募了 216 名参与者,其中 94 人为多动症儿童,122 人为 TD 儿童。ADHD组在顺行、逆行和延迟眨眼任务中的表现(准确率和完成时间)明显低于TD组。此外,在瞳孔直径波动、注视轨迹的规律性以及对无兴趣区域的固定等数字生物标志物方面也存在明显的组间差异。虽然随着时间的推移,多动症组的准确率和任务完成速度都有所提高,但他们的眼球运动模式仍然不规则。5-6 岁的 TD 组表现优于 9-10 岁的 ADHD 组,而且这种差异随着时间的推移保持相对稳定,这表明 ADHD 组遵循一种独特的发育模式。ML 模型能有效区分各组,其曲线下面积为 0.965,准确率为 0.908:本研究提出的眼动跟踪生物标志物能有效识别多动症组和注意力缺陷症组在眼动模式各个方面的差异。此外,利用这些数字生物标记构建的 ML 模型在鉴别 ADHD 方面具有很高的准确性和可靠性。我们的系统可以促进学校和社区对多动症的早期筛查,并为临床医生提供客观的生物标志物作为参考:本研究已在中国临床试验注册中心注册(编号:ChiCTR2400087697)。
{"title":"Auxiliary Diagnosis of Children With Attention-Deficit/Hyperactivity Disorder Using Eye-Tracking and Digital Biomarkers: Case-Control Study.","authors":"Zhongling Liu, Jinkai Li, Yuanyuan Zhang, Dan Wu, Yanyan Huo, Jianxin Yang, Musen Zhang, Chuanfei Dong, Luhui Jiang, Ruohan Sun, Ruoyin Zhou, Fei Li, Xiaodan Yu, Daqian Zhu, Yao Guo, Jinjin Chen","doi":"10.2196/58927","DOIUrl":"10.2196/58927","url":null,"abstract":"<p><strong>Background: </strong>Attention-deficit/hyperactivity disorder (ADHD) is a common neurodevelopmental disorder in school-aged children. The lack of objective biomarkers for ADHD often results in missed diagnoses or misdiagnoses, which lead to inappropriate or delayed interventions. Eye-tracking technology provides an objective method to assess children's neuropsychological behavior.</p><p><strong>Objective: </strong>The aim of this study was to develop an objective and reliable auxiliary diagnostic system for ADHD using eye-tracking technology. This system would be valuable for screening for ADHD in schools and communities and may help identify objective biomarkers for the clinical diagnosis of ADHD.</p><p><strong>Methods: </strong>We conducted a case-control study of children with ADHD and typically developing (TD) children. We designed an eye-tracking assessment paradigm based on the core cognitive deficits of ADHD and extracted various digital biomarkers that represented participant behaviors. These biomarkers and developmental patterns were compared between the ADHD and TD groups. Machine learning (ML) was implemented to validate the ability of the extracted eye-tracking biomarkers to predict ADHD. The performance of the ML models was evaluated using 5-fold cross-validation.</p><p><strong>Results: </strong>We recruited 216 participants, of whom 94 (43.5%) were children with ADHD and 122 (56.5%) were TD children. The ADHD group showed significantly poorer performance (for accuracy and completion time) than the TD group in the prosaccade, antisaccade, and delayed saccade tasks. In addition, there were substantial group differences in digital biomarkers, such as pupil diameter fluctuation, regularity of gaze trajectory, and fixations on unrelated areas. Although the accuracy and task completion speed of the ADHD group increased over time, their eye-movement patterns remained irregular. The TD group with children aged 5 to 6 years outperformed the ADHD group with children aged 9 to 10 years, and this difference remained relatively stable over time, which indicated that the ADHD group followed a unique developmental pattern. The ML model was effective in discriminating the groups, achieving an area under the curve of 0.965 and an accuracy of 0.908.</p><p><strong>Conclusions: </strong>The eye-tracking biomarkers proposed in this study effectively identified differences in various aspects of eye-movement patterns between the ADHD and TD groups. In addition, the ML model constructed using these digital biomarkers achieved high accuracy and reliability in identifying ADHD. Our system can facilitate early screening for ADHD in schools and communities and provide clinicians with objective biomarkers as a reference.</p>","PeriodicalId":14756,"journal":{"name":"JMIR mHealth and uHealth","volume":" ","pages":"e58927"},"PeriodicalIF":5.4,"publicationDate":"2024-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11645504/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142545606","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Evaluating the Impact of a Daylight-Simulating Luminaire on Mood, Agitation, Rest-Activity Patterns, and Social Well-Being Parameters in a Care Home for People With Dementia: Cohort Study. 评估模拟日光灯具对养老院中痴呆症患者的情绪、躁动、休息-活动模式和社会福利参数的影响:队列研究
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-11-29 DOI: 10.2196/56951
Kate Turley, Joseph Rafferty, Raymond Bond, Maurice Mulvenna, Assumpta Ryan, Lloyd Crawford

Background: Living with a diagnosis of dementia can involve managing certain behavioral and psychological symptoms. Alongside cognitive decline, this cohort expresses a suppression in melatonin production which can negatively influence their alignment of sleep or wake timings with the 24 hour day and night cycle. As a result, their circadian rhythms become disrupted. Since daylight has the capacity to stimulate the circadian rhythm and humans spend approximately 90% of their time indoors, research has shifted toward the use of indoor lighting to achieve this same effect. This type of lighting is programmed in a daylight-simulating manner; mimicking the spectral changes of the sun throughout the day. As such, this paper focuses on the use of a dynamic lighting and sensing technology used to support the circadian rhythm, behavioral and psychological symptoms, and well-being of people living with dementia.

Objective: This study aimed to understand how dynamic lighting, as opposed to static lighting, may impact the well-being of those who are living with dementia.

Methods: An ethically approved trial was conducted within a care home for people with dementia. Data were collected in both quantitative and qualitative formats using environmentally deployed radar sensing technology and the validated QUALIDEM (Quality of Life for People With Dementia) well-being scale, respectively. An initial 4 weeks of static baseline lighting was used before switching out for 12 weeks of dynamic lighting. Metrics were collected for 11 participants on mood, social interactions, agitation, sense of feeling, and sleep and rest-activity over a period of 16 weeks.

Results: Dynamic lighting showed significant improvement with a moderate effect size in well-being parameters including positive affect (P=.03), social isolation (P=.048), and feeling at home (P=.047) after 5-10 weeks of dynamic lighting exposure. The results also highlight statistically significant improvements in rest-activity-related parameters of interdaily stability (P<.001), intradaily variation (P<.001), and relative amplitude (P=.03) from baseline to weeks 5-10, with the effect propagating for interdaily stability at weeks 10-16 as well (P<.001). Nonsignificant improvements are also noted for sleep metrics with a small effect size; however, the affect in agitation does not reflect this improvement.

Conclusions: Dynamic lighting has the potential to support well-being in dementia, with seemingly stronger influence in earlier weeks where the dynamic lighting initially follows the static lighting contrast, before proceeding to aggregate as marginal gains over time. Future longitudinal studies are recommended to assess the additional impact that varying daylight availability throughout the year may have on the measured parameters.

背景:诊断为痴呆症的患者可能需要管理某些行为和心理症状。在认知能力下降的同时,该队列还表现出褪黑激素分泌的抑制,这可能会对他们的睡眠或醒来时间与24小时昼夜循环的一致性产生负面影响。结果,他们的昼夜节律被打乱了。由于日光具有刺激昼夜节律的能力,而人类大约90%的时间都在室内度过,因此研究已经转向使用室内照明来达到同样的效果。这种类型的照明以模拟日光的方式进行编程;模拟太阳全天的光谱变化。因此,本文侧重于使用动态照明和传感技术来支持痴呆症患者的昼夜节律、行为和心理症状以及福祉。目的:本研究旨在了解动态照明,而不是静态照明,如何影响痴呆症患者的健康。方法:一项经伦理批准的试验在一家老年痴呆症患者护理中心进行。数据分别采用环境部署雷达传感技术和经过验证的QUALIDEM(痴呆症患者生活质量)健康量表,以定量和定性两种格式收集。最初4周使用静态基线照明,然后切换到12周的动态照明。在16周的时间里,研究人员收集了11名参与者的情绪、社交互动、躁动、感觉、睡眠和休息活动等指标。结果:在5-10周的动态照明后,动态照明在积极情绪(P=.03)、社会隔离(P=.048)和家的感觉(P=.047)等幸福感参数上有显著改善。研究结果还强调了在休息-活动相关的日常稳定性参数方面的统计学显著改善(pp结论:动态照明有可能支持痴呆症患者的健康,在最初的几周内,动态照明的影响似乎更大,在此之前,动态照明最初遵循静态照明的对比,然后随着时间的推移逐渐累积为边际收益。建议未来进行纵向研究,以评估全年不同的日光可用性可能对测量参数产生的额外影响。
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引用次数: 0
An Evaluation of the Effect of App-Based Exercise Prescription Using Reinforcement Learning on Satisfaction and Exercise Intensity: Randomized Crossover Trial. 基于app的强化学习运动处方对满意度和运动强度的影响评价:随机交叉试验。
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-11-26 DOI: 10.2196/49443
Cailbhe Doherty, Rory Lambe, Ben O'Grady, Diarmuid O'Reilly-Morgan, Barry Smyth, Aonghus Lawlor, Neil Hurley, Elias Tragos
<p><strong>Background: </strong>The increasing prevalence of sedentary lifestyles has prompted the development of innovative public health interventions, such as smartphone apps that deliver personalized exercise programs. The widespread availability of mobile technologies (eg, smartphone apps and wearable activity trackers) provides a cost-effective, scalable way to remotely deliver personalized exercise programs to users. Using machine learning (ML), specifically reinforcement learning (RL), may enhance user engagement and effectiveness of these programs by tailoring them to individual preferences and needs.</p><p><strong>Objective: </strong>The primary aim was to investigate the impact of the Samsung-developed i80 BPM app, implementing ML for exercise prescription, on user satisfaction and exercise intensity among the general population. The secondary objective was to assess the effectiveness of ML-generated exercise programs for remote prescription of exercise to members of the public.</p><p><strong>Methods: </strong>Participants were randomized to complete 3 exercise sessions per week for 12 weeks using the i80 BPM mobile app, crossing over weekly between intervention and control conditions. The intervention condition involved individualizing exercise sessions using RL, based on user preferences such as exercise difficulty, selection, and intensity, whereas under the control condition, exercise sessions were not individualized. Exercise intensity (measured by the 10-item Borg scale) and user satisfaction (measured by the 8-item version of the Physical Activity Enjoyment Scale) were recorded after the session.</p><p><strong>Results: </strong>In total, 62 participants (27 male and 42 female participants; mean age 43, SD 13 years) completed 559 exercise sessions over 12 weeks (9 sessions per participant). Generalized estimating equations showed that participants were more likely to exercise at a higher intensity (intervention: mean intensity 5.82, 95% CI 5.59-6.05 and control: mean intensity 5.19, 95% CI 4.97-5.41) and report higher satisfaction (RL: mean satisfaction 4, 95% CI 3.9-4.1 and baseline: mean satisfaction 3.73, 95% CI 3.6-3.8) in the RL model condition.</p><p><strong>Conclusions: </strong>The findings suggest that RL can effectively increase both the intensity with which people exercise and their enjoyment of the sessions, highlighting the potential of ML to enhance remote exercise interventions. This study underscores the benefits of personalized exercise prescriptions in increasing adherence and satisfaction, which are crucial for the long-term effectiveness of fitness programs. Further research is warranted to explore the long-term impacts and potential scalability of RL-enhanced exercise apps in diverse populations. This study contributes to the understanding of digital health interventions in exercise science, suggesting that personalized, app-based exercise prescriptions may be more effective than traditional, nonpersonalized
背景:久坐不动的生活方式越来越普遍,促使了创新公共卫生干预措施的发展,例如提供个性化锻炼计划的智能手机应用程序。移动技术的广泛应用(如智能手机应用程序和可穿戴式活动追踪器)为用户远程提供个性化锻炼计划提供了一种经济、可扩展的方式。使用机器学习(ML),特别是强化学习(RL),可以根据个人偏好和需求定制这些程序,从而提高用户参与度和有效性。目的:主要目的是调查三星开发的i80 BPM应用程序对普通人群的用户满意度和运动强度的影响,该应用程序实现了运动处方的ML。第二个目标是评估机器学习生成的运动计划对公众远程运动处方的有效性。方法:参与者被随机分配到使用i80 BPM移动应用程序每周完成3次锻炼,持续12周,在干预和控制条件之间跨越每周。干预条件是根据用户偏好(如运动难度、选择和强度)使用强化学习对运动进行个性化,而在控制条件下,运动不进行个性化。运动强度(由10项博格量表测量)和用户满意度(由8项体育活动享受量表测量)在会议结束后被记录下来。结果:共纳入受试者62人(男27人,女42人);平均年龄43岁,SD 13岁)在12周内完成559次锻炼(每位参与者9次)。广义估计方程显示,在RL模型条件下,参与者更有可能以更高的强度进行运动(干预:平均强度5.82,95% CI 5.59-6.05,对照组:平均强度5.19,95% CI 4.97-5.41),并报告更高的满意度(RL:平均满意度4,95% CI 3.9-4.1,基线:平均满意度3.73,95% CI 3.6-3.8)。结论:研究结果表明,RL可以有效地增加人们锻炼的强度和他们对锻炼的享受,突出了ML增强远程锻炼干预的潜力。这项研究强调了个性化运动处方在提高坚持性和满意度方面的好处,这对健身计划的长期有效性至关重要。进一步的研究是有必要的,以探索长期影响和潜在的可扩展性的强化训练应用程序在不同的人群。这项研究有助于理解运动科学中的数字健康干预措施,表明个性化的、基于应用程序的运动处方可能比传统的、非个性化的方法更有效。将RL整合到锻炼应用程序中可以显著影响公众健康,特别是在提高参与度和减轻全球缺乏体育锻炼的负担方面。
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