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Mobile App Intervention to Reduce Substance Use, Gambling, and Digital Media Use in Vocational School Students: Exploratory Analysis of the Intervention Arm of a Randomized Controlled Trial. 减少职业学校学生药物使用、赌博和数字媒体使用的手机应用干预:随机对照试验干预组的探索性分析。
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-07-23 DOI: 10.2196/51307
Kristin Grahlher, Matthis Morgenstern, Benjamin Pietsch, Elena Gomes de Matos, Monika Rossa, Kirsten Lochbühler, Anne Daubmann, Rainer Thomasius, Nicolas Arnaud
<p><strong>Background: </strong>During adolescence, substance use and digital media exposure usually peak and can become major health risks. Prevention activities are mainly implemented in the regular school setting, and youth outside this system are not reached. A mobile app ("Meine Zeit ohne") has been developed specifically for vocational students and encourages participants to voluntarily reduce or abstain from a self-chosen addictive behavior including the use of a substance, gambling, or a media-related habit such as gaming or social media use for 2 weeks. Results from a randomized study indicate a significant impact on health-promoting behavior change after using the app. This exploratory study focuses on the intervention arm of this study, focusing on acceptance and differential effectiveness.</p><p><strong>Objective: </strong>The aims of this study were (1) to examine the characteristics of participants who used the app, (2) to explore the effectiveness of the mobile intervention depending on how the app was used and depending on participants' characteristics, and (3) to study how variations in app use were related to participants' baseline characteristics.</p><p><strong>Methods: </strong>Log data from study participants in the intervention group were analyzed including the frequency of app use (in days), selection of a specific challenge, and personal relevance (ie, the user was above a predefined risk score for a certain addictive behavior) of challenge selection ("congruent use": eg, a smoker selected a challenge related to reducing or quitting smoking). Dichotomous outcomes (change vs no change) referred to past-month substance use, gambling, and media-related behaviors. The relationship between these variables was analyzed using binary, multilevel, mixed-effects logistic regression models.</p><p><strong>Results: </strong>The intervention group consisted of 2367 vocational students, and 1458 (61.6%; mean age 19.0, SD 3.5 years; 830/1458, 56.9% male) of them provided full data. Of these 1458 students, 894 (61.3%) started a challenge and could be included in the analysis (mean 18.7, SD 3.5 years; 363/894, 40.6% female). Of these 894 students, 466 (52.1%) were considered frequent app users with more than 4 days of active use over the 2-week period. The challenge area most often chosen in the analyzed sample was related to social media use (332/894, 37.1%). A total of 407 (45.5%) of the 894 students selected a challenge in a behavioral domain of personal relevance. The effects of app use on outcomes were higher when the area of individual challenge choice was equal to the area of behavior change, challenge choice was related to a behavior of personal relevance, and the individual risk of engaging in different addictive behaviors was high.</p><p><strong>Conclusions: </strong>The domain-specific effectiveness of the program was confirmed with no spillover between behavioral domains. Effectiveness appeared to be dependent on app use and use
背景介绍青少年时期通常是使用药物和接触数字媒体的高峰期,并可能成为主要的健康风险。预防活动主要是在正规学校环境中开展的,没有接触到这一系统之外的青少年。我们专门为职业学校学生开发了一款手机应用程序("Meine Zeit ohne"),鼓励参与者在两周内自愿减少或戒除自我选择的成瘾行为,包括使用药物、赌博或与媒体相关的习惯,如游戏或社交媒体使用。一项随机研究的结果表明,使用该应用程序后,对促进健康的行为改变有显著影响。本探索性研究的重点是该研究的干预部分,关注接受度和不同效果:本研究的目的是:(1) 检查使用该应用的参与者的特征;(2) 根据应用的使用方式和参与者的特征,探讨移动干预的有效性;(3) 研究应用使用的变化与参与者基线特征的关系:对干预组研究参与者的日志数据进行了分析,包括应用程序的使用频率(以天为单位)、特定挑战的选择以及挑战选择的个人相关性(即用户超过了某种成瘾行为的预定风险分值)("一致使用":例如,吸烟者选择了与减少或戒烟相关的挑战)。二分结果(有变化与无变化)指的是上个月的药物使用、赌博和媒体相关行为。这些变量之间的关系采用二元、多层次、混合效应逻辑回归模型进行分析:干预组由 2367 名职业学生组成,其中 1458 人(61.6%;平均年龄 19.0 岁,标准差 3.5 岁;830/1458,56.9% 为男性)提供了完整的数据。在这 1458 名学生中,有 894 人(61.3%)开始接受挑战,可以纳入分析(平均年龄为 18.7 岁,标准差为 3.5 岁;363/894,40.6% 为女性)。在这 894 名学生中,有 466 人(52.1%)被认为是应用程序的频繁用户,在两周时间内活跃使用超过 4 天。分析样本中最常选择的挑战领域与社交媒体的使用有关(332/894,37.1%)。在 894 名学生中,共有 407 人(45.5%)选择了与个人相关的行为领域的挑战。当个人选择的挑战领域与行为改变领域相同、选择的挑战与个人相关行为有关以及个人参与不同成瘾行为的风险较高时,应用程序的使用对结果的影响更大:结论:该计划在特定领域的有效性得到了证实,行为领域之间没有溢出效应。有效性似乎取决于应用程序的使用和用户的特征:德国临床试验注册中心 DRKS00023788;https://tinyurl.com/4pzpjkmj.International 注册报告标识符(irrid):RR2-10.1186/s13063-022-06231-x.
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引用次数: 0
Conversational Chatbot for Cigarette Smoking Cessation: Results From the 11-Step User-Centered Design Development Process and Randomized Controlled Trial. 戒烟对话聊天机器人:用户中心设计十一步开发流程报告》。
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-07-23 DOI: 10.2196/57318
Jonathan B Bricker, Brianna Sullivan, Kristin Mull, Margarita Santiago-Torres, Juan M Lavista Ferres
<p><strong>Background: </strong>Conversational chatbots are an emerging digital intervention for smoking cessation. No studies have reported on the entire development process of a cessation chatbot.</p><p><strong>Objective: </strong>We aim to report results of the user-centered design development process and randomized controlled trial for a novel and comprehensive quit smoking conversational chatbot called QuitBot.</p><p><strong>Methods: </strong>The 4 years of formative research for developing QuitBot followed an 11-step process: (1) specifying a conceptual model; (2) conducting content analysis of existing interventions (63 hours of intervention transcripts); (3) assessing user needs; (4) developing the chat's persona ("personality"); (5) prototyping content and persona; (6) developing full functionality; (7) programming the QuitBot; (8) conducting a diary study; (9) conducting a pilot randomized controlled trial (RCT); (10) reviewing results of the RCT; and (11) adding a free-form question and answer (QnA) function, based on user feedback from pilot RCT results. The process of adding a QnA function itself involved a three-step process: (1) generating QnA pairs, (2) fine-tuning large language models (LLMs) on QnA pairs, and (3) evaluating the LLM outputs.</p><p><strong>Results: </strong>We developed a quit smoking program spanning 42 days of 2- to 3-minute conversations covering topics ranging from motivations to quit, setting a quit date, choosing Food and Drug Administration-approved cessation medications, coping with triggers, and recovering from lapses and relapses. In a pilot RCT with 96% three-month outcome data retention, QuitBot demonstrated high user engagement and promising cessation rates compared to the National Cancer Institute's SmokefreeTXT text messaging program, particularly among those who viewed all 42 days of program content: 30-day, complete-case, point prevalence abstinence rates at 3-month follow-up were 63% (39/62) for QuitBot versus 38.5% (45/117) for SmokefreeTXT (odds ratio 2.58, 95% CI 1.34-4.99; P=.005). However, Facebook Messenger intermittently blocked participants' access to QuitBot, so we transitioned from Facebook Messenger to a stand-alone smartphone app as the communication channel. Participants' frustration with QuitBot's inability to answer their open-ended questions led to us develop a core conversational feature, enabling users to ask open-ended questions about quitting cigarette smoking and for the QuitBot to respond with accurate and professional answers. To support this functionality, we developed a library of 11,000 QnA pairs on topics associated with quitting cigarette smoking. Model testing results showed that Microsoft's Azure-based QnA maker effectively handled questions that matched our library of 11,000 QnA pairs. A fine-tuned, contextualized GPT-3.5 (OpenAI) responds to questions that are not within our library of QnA pairs.</p><p><strong>Conclusions: </strong>The development process yielded t
背景对话聊天机器人是一种新兴的戒烟数字干预方法。目前还没有关于戒烟聊天机器人整个开发过程的研究报告:目的:描述一款名为 "戒烟机器人"(QuitBot)的新颖、全面的戒烟对话式聊天机器人以用户为中心的设计开发过程:开发 QuitBot 的四年形成性研究经历了十一个步骤:(1)确定概念模型;(2)对现有干预措施进行内容分析(63 小时的干预记录);(3)评估用户需求;(4)开发聊天角色("个性");(5)内容和角色原型;(6)开发全部功能、(7) 编写戒烟机器人程序,(8) 进行日记研究,(9) 进行试点随机试验,(10) 审查试验结果,(11) 根据试点试验结果中的用户反馈添加自由问答(QnA)功能。添加 QnA 功能的过程本身包括三个步骤:(a) 生成 QnA 对,(b) 微调 QnA 对上的大型语言模型 (LLM),(c) 评估 LLM 模型输出:一项为期 42 天的戒烟计划由 2 到 3 分钟的对话组成,对话主题包括戒烟动机、设定戒烟日期、选择 FDA 批准的戒烟药物、应对诱因以及从失误/复吸中恢复。在一项试点随机试验中,三个月的结果数据保留率为96%,与美国国家癌症研究所的SmokefreeTXT(SFT)短信项目相比,QuitBot的用户参与度很高,戒烟率也很可观--尤其是那些观看了全部42天项目内容的用户:在三个月的随访中,QuitBot的30天完全戒烟率(PPA)为63%(39/62),而SFT为38%(45/117)(OR = 2.58; 95% CI: 1.34, 4.99; P =.005)。然而,Facebook Messenger(FM)间歇性地阻止了参与者访问 QuitBot,因此我们将 FM 转换为独立的智能手机应用程序作为交流渠道。参与者对戒烟机器人无法回答他们的开放式问题感到沮丧,这促使我们开发了一项核心对话功能,使用户能够提出有关戒烟的开放式问题,并让戒烟机器人做出准确、专业的回答。为了支持这一功能,我们开发了一个包含 11,000 对戒烟相关主题的 QnA 库。模型测试结果表明,微软基于 Azure 的 QnA 制造商能够有效处理与我们的 11,000 对 QnA 库相匹配的问题。经过微调、符合上下文的 GPT3.5 可应对不在我们的 QnA 对库中的问题:开发过程产生了第一个基于 LLM 的戒烟程序,该程序以对话聊天机器人的形式提供。迭代测试带来了重大改进,包括交付渠道的改进。一个关键的新增功能是加入了由 LLM 支持的核心对话功能,允许用户提出开放式问题:临床试验:ClinicalTrials.gov Identifier,NCT03585231。
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引用次数: 0
Feasibility and Preliminary Effects of a Social Media-Based Peer-Group Mobile Messaging Smoking Cessation Intervention Among Chinese Immigrants who Smoke: Pilot Randomized Controlled Trial. 在吸烟的中国移民中开展基于社交媒体的同伴小组移动信息戒烟干预的可行性和初步效果:试点随机对照试验》。
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-07-22 DOI: 10.2196/59496
Nan Jiang, Ariel Zhao, Erin S Rogers, Ana Paula Cupertino, Xiaoquan Zhao, Francisco Cartujano-Barrera, Katherine Siu, Scott E Sherman
<p><strong>Background: </strong>Chinese immigrants experience significant disparities in tobacco use. Culturally adapted tobacco treatments targeting this population are sparse and the use is low. The low use of these treatment programs is attributed to their exclusive focus on individuals who are ready to quit and the wide range of barriers that Chinese immigrants face to access these programs. To support Chinese immigrant smokers at all levels of readiness to quit and address their access barriers, we developed the WeChat Quit Coach, a culturally and linguistically appropriate WeChat (Tencent Holdings Limited)-based peer group mobile messaging smoking cessation intervention.</p><p><strong>Objective: </strong>This study aims to assess the feasibility, acceptability, and preliminary effects of WeChat Quit Coach.</p><p><strong>Methods: </strong>We enrolled a total of 60 Chinese immigrant smokers in 2022 in New York City for a pilot randomized controlled trial (RCT) and a single-arm pilot test. The first 40 participants were randomized to either the intervention arm (WeChat Quit Coach) or the control arm (self-help print material) using 1:1 block randomization stratified by sex. WeChat Quit Coach lasted 6 weeks, featuring small peer groups moderated by a coach, daily text messages with text questions, and chat-based instant messaging support from the coach in response to peer questions. The next 20 participants were enrolled in the single-arm pilot test to further assess intervention feasibility and acceptability. All 60 participants were offered a 4-week supply of complimentary nicotine replacement therapy. Surveys were administered at baseline and 6 weeks, with participants in the pilot RCT completing an additional survey at 6 months and biochemical verification of abstinence at both follow-ups.</p><p><strong>Results: </strong>Of 74 individuals screened, 68 (92%) were eligible and 60 (88%) were enrolled. The majority of participants, with a mean age of 42.5 (SD 13.8) years, were male (49/60, 82%) and not ready to quit, with 70% (42/60) in the precontemplation or contemplation stage at the time of enrollment. The pilot RCT had follow-up rates of 98% (39/40) at 6 weeks and 93% (37/40) at 6 months, while the single-arm test achieved 100% follow-up at 6 weeks. On average, participants responded to daily text questions for 25.1 days over the 42-day intervention period and 23% (9/40) used the chat-based instant messaging support. Most participants were satisfied with WeChat Quit Coach (36/39, 92%) and would recommend it to others (32/39, 82%). At 6 months, self-reported 7-day point prevalence abstinence rates were 25% (5/20) in the intervention arm and 15% (3/20) in the control arm, with biochemically verified abstinence rates of 25% (5/20) and 5% (1/20), respectively.</p><p><strong>Conclusions: </strong>WeChat Quit Coach was feasible and well-received by Chinese immigrants who smoke and produced promising effects on abstinence. Large trials are warran
背景:中国移民在烟草使用方面存在很大差异。针对这一人群的适应文化的烟草治疗项目很少,使用率也很低。这些治疗项目之所以使用率低,是因为它们只针对准备戒烟的人,而且华裔移民在使用这些项目时面临各种障碍。为了支持处于不同戒烟准备水平的中国移民吸烟者,并解决他们的戒烟障碍,我们开发了 "微信戒烟教练",这是一种基于微信(腾讯控股有限公司)的同侪群移动信息戒烟干预措施,适合不同的文化和语言:本研究旨在评估微信戒烟教练的可行性、可接受性和初步效果:2022 年,我们在纽约市共招募了 60 名中国移民吸烟者,进行随机对照试验(RCT)和单臂试点测试。首批40名参与者按性别分层,以1:1整群随机方式被随机分配到干预组(微信戒烟教练)或对照组(自助印刷材料)。微信戒烟教练 "为期 6 周,主要内容包括由教练主持的小型同伴小组、包含文字问题的每日短信,以及教练针对同伴提出的问题提供的即时聊天支持。接下来的 20 名参与者参加了单臂试点测试,以进一步评估干预的可行性和可接受性。所有 60 名参与者都获得了为期 4 周的免费尼古丁替代疗法。在基线和 6 周时进行调查,试点 RCT 的参与者在 6 个月时完成额外的调查,并在两次随访时完成戒烟的生化验证:在筛选出的 74 人中,68 人(92%)符合条件,60 人(88%)被录取。大多数参与者的平均年龄为 42.5 岁(标准差为 13.8 岁),男性(49/60,82%),尚未做好戒烟准备,70%(42/60)的参与者在报名时处于前考虑或考虑阶段。试点 RCT 的 6 周随访率为 98%(39/40),6 个月随访率为 93%(37/40),而单臂试验的 6 周随访率为 100%。在为期 42 天的干预期间,参与者平均每天回复文字问题 25.1 天,23%(9/40)的参与者使用了基于聊天的即时信息支持。大多数参与者对微信戒烟教练感到满意(36/39,92%),并愿意向他人推荐(32/39,82%)。6个月后,干预组的自我报告7天点戒断率为25%(5/20),对照组为15%(3/20),经生化验证的戒断率分别为25%(5/20)和5%(1/20):结论:微信戒烟教练是可行的,深受中国吸烟移民的欢迎,对戒烟产生了良好的效果。有必要进行大规模试验,以评估其在这一服务不足人群中促进戒烟的效果:试验注册:ClinicalTrials.gov NCT05130788;https://clinicaltrials.gov/study/NCT05130788。
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引用次数: 0
Identifying Weekly Trajectories of Pain Severity Using Daily Data From an mHealth Study: Cluster Analysis. 利用移动医疗研究的每日数据识别疼痛严重程度的每周轨迹:聚类分析。
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-07-19 DOI: 10.2196/48582
Claire L Little, David M Schultz, Thomas House, William G Dixon, John McBeth
<p><strong>Background: </strong>People with chronic pain experience variability in their trajectories of pain severity. Previous studies have explored pain trajectories by clustering sparse data; however, to understand daily pain variability, there is a need to identify clusters of weekly trajectories using daily pain data. Between-week variability can be explored by quantifying the week-to-week movement between these clusters. We propose that future work can use clusters of pain severity in a forecasting model for short-term (eg, daily fluctuations) and longer-term (eg, weekly patterns) variability. Specifically, future work can use clusters of weekly trajectories to predict between-cluster movement and within-cluster variability in pain severity.</p><p><strong>Objective: </strong>This study aims to understand clusters of common weekly patterns as a first stage in developing a pain-forecasting model.</p><p><strong>Methods: </strong>Data from a population-based mobile health study were used to compile weekly pain trajectories (n=21,919) that were then clustered using a k-medoids algorithm. Sensitivity analyses tested the impact of assumptions related to the ordinal and longitudinal structure of the data. The characteristics of people within clusters were examined, and a transition analysis was conducted to understand the movement of people between consecutive weekly clusters.</p><p><strong>Results: </strong>Four clusters were identified representing trajectories of no or low pain (1714/21,919, 7.82%), mild pain (8246/21,919, 37.62%), moderate pain (8376/21,919, 38.21%), and severe pain (3583/21,919, 16.35%). Sensitivity analyses confirmed the 4-cluster solution, and the resulting clusters were similar to those in the main analysis, with at least 85% of the trajectories belonging to the same cluster as in the main analysis. Male participants spent longer (participant mean 7.9, 95% bootstrap CI 6%-9.9%) in the no or low pain cluster than female participants (participant mean 6.5, 95% bootstrap CI 5.7%-7.3%). Younger people (aged 17-24 y) spent longer (participant mean 28.3, 95% bootstrap CI 19.3%-38.5%) in the severe pain cluster than older people (aged 65-86 y; participant mean 9.8, 95% bootstrap CI 7.7%-12.3%). People with fibromyalgia (participant mean 31.5, 95% bootstrap CI 28.5%-34.4%) and neuropathic pain (participant mean 31.1, 95% bootstrap CI 27.3%-34.9%) spent longer in the severe pain cluster than those with other conditions, and people with rheumatoid arthritis spent longer (participant mean 7.8, 95% bootstrap CI 6.1%-9.6%) in the no or low pain cluster than those with other conditions. There were 12,267 pairs of consecutive weeks that contributed to the transition analysis. The empirical percentage remaining in the same cluster across consecutive weeks was 65.96% (8091/12,267). When movement between clusters occurred, the highest percentage of movement was to an adjacent cluster.</p><p><strong>Conclusions: </strong>The clusters of pain
背景:慢性疼痛患者的疼痛严重程度的变化轨迹是多变的。以往的研究通过对稀疏数据进行聚类来探索疼痛轨迹;然而,要了解每日疼痛的变异性,需要利用每日疼痛数据确定每周轨迹的聚类。通过量化这些聚类之间的周间移动,可以探索周间变异性。我们建议,未来的工作可以在短期(如每日波动)和长期(如每周模式)变异性预测模型中使用疼痛严重程度集群。具体来说,未来的工作可以利用每周轨迹集群来预测疼痛严重程度的集群间移动和集群内变化:本研究旨在了解常见的每周模式群,作为开发疼痛预测模型的第一阶段:方法:利用一项基于人群的移动健康研究数据编制每周疼痛轨迹(n=21,919),然后使用 K-medoids 算法对这些轨迹进行聚类。敏感性分析测试了与数据的顺序和纵向结构相关的假设的影响。对聚类内人群的特征进行了研究,并进行了过渡分析,以了解人群在连续的周聚类之间的流动情况:结果:发现了四个群组,分别代表无痛或低痛(1714/211919,7.82%)、轻度疼痛(8246/211919,37.62%)、中度疼痛(8376/211919,38.21%)和重度疼痛(3583/211919,16.35%)的轨迹。敏感性分析确认了 4 个群组的解决方案,得出的群组与主要分析中的群组相似,至少有 85% 的轨迹与主要分析中的轨迹属于同一群组。男性参与者在无痛或低痛聚类中花费的时间(参与者平均值为 7.9,95% bootstrap CI 为 6%-9.9%)长于女性参与者(参与者平均值为 6.5,95% bootstrap CI 为 5.7%-7.3%)。年轻人(17-24 岁)在严重疼痛组中的时间(参与者平均 28.3,95% 自举系数 CI 19.3%-38.5%)长于老年人(65-86 岁;参与者平均 9.8,95% 自举系数 CI 7.7%-12.3%)。纤维肌痛(参与者平均值为 31.5,95% bootstrap CI 为 28.5%-34.4%)和神经病理性疼痛(参与者平均值为 31.1,95% bootstrap CI 为 27.3%-34.9%)患者在重度疼痛群组中的时间比其他疾病患者长,类风湿性关节炎患者在无痛或低度疼痛群组中的时间(参与者平均值为 7.8,95% bootstrap CI 为 6.1%-9.6%)比其他疾病患者长。共有 12,267 对连续周数参与了过渡分析。在连续几周内保持在同一群组的经验百分比为 65.96%(8091/12267)。当组群之间发生移动时,移动到相邻组群的比例最高:本研究确定的疼痛严重程度群组对慢性疼痛患者每周的经历进行了简洁的描述。这些群组可用于今后对群组间移动和群组内变异性的研究,从而开发出准确的、由利益相关者提供信息的疼痛预测工具。
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引用次数: 0
Continuous Monitoring of Heart Rate Variability and Respiration for the Remote Diagnosis of Chronic Obstructive Pulmonary Disease: Prospective Observational Study. 连续监测心率变异性和呼吸以远程诊断慢性阻塞性肺病:前瞻性观察研究
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-07-18 DOI: 10.2196/56226
Xiaolan Chen, Han Zhang, Zhiwen Li, Shuang Liu, Yuqi Zhou

Background: Conventional daytime monitoring in a single day may be influenced by factors such as motion artifacts and emotions, and continuous monitoring of nighttime heart rate variability (HRV) and respiration to assist in chronic obstructive pulmonary disease (COPD) diagnosis has not been reported yet.

Objective: The aim of this study was to explore and compare the effects of continuously monitored HRV, heart rate (HR), and respiration during night sleep on the remote diagnosis of COPD.

Methods: We recruited patients with different severities of COPD and healthy controls between January 2021 and November 2022. Vital signs such as HRV, HR, and respiration were recorded using noncontact bed sensors from 10 PM to 8 AM of the following day, and the recordings of each patient lasted for at least 30 days. We obtained statistical means of HRV, HR, and respiration over time periods of 7, 14, and 30 days by continuous monitoring. Additionally, the effects that the statistical means of HRV, HR, and respiration had on COPD diagnosis were evaluated at different times of recordings.

Results: In this study, 146 individuals were enrolled: 37 patients with COPD in the case group and 109 participants in the control group. The median number of continuous night-sleep monitoring days per person was 56.5 (IQR 32.0-113.0) days. Using the features regarding the statistical means of HRV, HR, and respiration over 1, 7, 14, and 30 days, binary logistic regression classification of COPD yielded an accuracy, Youden index, and area under the receiver operating characteristic curve of 0.958, 0.904, and 0.989, respectively. The classification performance for COPD diagnosis was directionally proportional to the monitoring duration of vital signs at night. The importance of the features for diagnosis was determined by the statistical means of respiration, HRV, and HR, which followed the order of respiration > HRV > HR. Specifically, the statistical means of the duration of respiration rate faster than 21 times/min (RRF), high frequency band power of 0.15-0.40 Hz (HF), and respiration rate (RR) were identified as the top 3 most significant features for classification, corresponding to cutoff values of 0.1 minute, 1316.3 nU, and 16.3 times/min, respectively.

Conclusions: Continuous monitoring of nocturnal vital signs has significant potential for the remote diagnosis of COPD. As the duration of night-sleep monitoring increased from 1 to 30 days, the statistical means of HRV, HR, and respiration showed a better reflection of an individual's health condition compared to monitoring the vital signs in a single day or night, and better was the classification performance for COPD diagnosis. Further, the statistical means of RRF, HF, and RR are crucial features for diagnosing COPD, demonstrating the importance of monitoring HRV and respiration during night sleep.

背景:传统的单日日间监测可能会受到运动伪影和情绪等因素的影响,而连续监测夜间心率变异性(HRV)和呼吸以辅助慢性阻塞性肺病(COPD)诊断的研究尚未见报道:本研究旨在探讨和比较夜间睡眠时连续监测心率变异、心率(HR)和呼吸对慢性阻塞性肺病远程诊断的影响:我们在 2021 年 1 月至 2022 年 11 月期间招募了不同严重程度的慢性阻塞性肺病患者和健康对照组。使用非接触式床用传感器记录晚上 10 点至次日早上 8 点的心率变异、心率和呼吸等生命体征,每位患者的记录至少持续 30 天。通过连续监测,我们获得了心率变异、心率和呼吸在 7 天、14 天和 30 天时间段内的统计平均值。此外,我们还评估了不同记录时间内心率变异、心率和呼吸的统计平均值对慢性阻塞性肺病诊断的影响:本研究共招募了 146 人:结果:这项研究共招募了 146 人:病例组中有 37 名慢性阻塞性肺病患者,对照组中有 109 人。每人连续夜间睡眠监测天数的中位数为 56.5 天(IQR 32.0-113.0)。利用 1、7、14 和 30 天内心率变异、心率和呼吸的统计平均值特征,对慢性阻塞性肺病进行二元逻辑回归分类,其准确率、尤登指数和接收者操作特征曲线下面积分别为 0.958、0.904 和 0.989。慢性阻塞性肺病诊断的分类效果与夜间生命体征监测持续时间成正比。特征对诊断的重要性由呼吸、心率变异和心率的统计均值决定,其顺序为呼吸>心率变异>心率。具体而言,呼吸频率快于 21 次/分(RRF)、0.15-0.40 Hz 的高频段功率(HF)和呼吸频率(RR)的统计均值被确定为最重要的前 3 个分类特征,分别对应于 0.1 分钟、1316.3 nU 和 16.3 次/分的临界值:结论:连续监测夜间生命体征对慢性阻塞性肺病的远程诊断具有重大潜力。随着夜间睡眠监测时间从 1 天增加到 30 天,心率变异、心率和呼吸的统计均值与单日或单夜生命体征监测相比,能更好地反映个体的健康状况,对慢性阻塞性肺疾病诊断的分类效果也更好。此外,RRF、HF 和 RR 的统计均值是诊断慢性阻塞性肺病的关键特征,这表明在夜间睡眠时监测心率变异和呼吸的重要性。
{"title":"Continuous Monitoring of Heart Rate Variability and Respiration for the Remote Diagnosis of Chronic Obstructive Pulmonary Disease: Prospective Observational Study.","authors":"Xiaolan Chen, Han Zhang, Zhiwen Li, Shuang Liu, Yuqi Zhou","doi":"10.2196/56226","DOIUrl":"10.2196/56226","url":null,"abstract":"<p><strong>Background: </strong>Conventional daytime monitoring in a single day may be influenced by factors such as motion artifacts and emotions, and continuous monitoring of nighttime heart rate variability (HRV) and respiration to assist in chronic obstructive pulmonary disease (COPD) diagnosis has not been reported yet.</p><p><strong>Objective: </strong>The aim of this study was to explore and compare the effects of continuously monitored HRV, heart rate (HR), and respiration during night sleep on the remote diagnosis of COPD.</p><p><strong>Methods: </strong>We recruited patients with different severities of COPD and healthy controls between January 2021 and November 2022. Vital signs such as HRV, HR, and respiration were recorded using noncontact bed sensors from 10 PM to 8 AM of the following day, and the recordings of each patient lasted for at least 30 days. We obtained statistical means of HRV, HR, and respiration over time periods of 7, 14, and 30 days by continuous monitoring. Additionally, the effects that the statistical means of HRV, HR, and respiration had on COPD diagnosis were evaluated at different times of recordings.</p><p><strong>Results: </strong>In this study, 146 individuals were enrolled: 37 patients with COPD in the case group and 109 participants in the control group. The median number of continuous night-sleep monitoring days per person was 56.5 (IQR 32.0-113.0) days. Using the features regarding the statistical means of HRV, HR, and respiration over 1, 7, 14, and 30 days, binary logistic regression classification of COPD yielded an accuracy, Youden index, and area under the receiver operating characteristic curve of 0.958, 0.904, and 0.989, respectively. The classification performance for COPD diagnosis was directionally proportional to the monitoring duration of vital signs at night. The importance of the features for diagnosis was determined by the statistical means of respiration, HRV, and HR, which followed the order of respiration > HRV > HR. Specifically, the statistical means of the duration of respiration rate faster than 21 times/min (RRF), high frequency band power of 0.15-0.40 Hz (HF), and respiration rate (RR) were identified as the top 3 most significant features for classification, corresponding to cutoff values of 0.1 minute, 1316.3 nU, and 16.3 times/min, respectively.</p><p><strong>Conclusions: </strong>Continuous monitoring of nocturnal vital signs has significant potential for the remote diagnosis of COPD. As the duration of night-sleep monitoring increased from 1 to 30 days, the statistical means of HRV, HR, and respiration showed a better reflection of an individual's health condition compared to monitoring the vital signs in a single day or night, and better was the classification performance for COPD diagnosis. Further, the statistical means of RRF, HF, and RR are crucial features for diagnosing COPD, demonstrating the importance of monitoring HRV and respiration during night sleep.</p>","PeriodicalId":14756,"journal":{"name":"JMIR mHealth and uHealth","volume":"12 ","pages":"e56226"},"PeriodicalIF":5.4,"publicationDate":"2024-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11294786/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141723679","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
Acceptability, Effectiveness, and Roles of mHealth Applications in Supporting Cancer Pain Self-Management: Integrative Review. 移动医疗应用在支持癌症疼痛自我管理中的可接受性、有效性和作用:综合评论。
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-07-18 DOI: 10.2196/53652
Weizi Wu, Teresa Graziano, Andrew Salner, Ming-Hui Chen, Michelle P Judge, Xiaomei Cong, Wanli Xu

Background:  Cancer pain remains highly prevalent and persistent throughout survivorship, and it is crucial to investigate the potential of leveraging the advanced features of mobile health (mHealth) apps to empower individuals to self-manage their pain.

Objective:  This review aims to comprehensively understand the acceptability, users' experiences, and effectiveness of mHealth apps in supporting cancer pain self-management.

Methods:  We conducted an integrative review following Souza and Whittemore and Knafl's 6 review processes. Literature was searched in PubMed, Scopus, CINAHL Plus with Full Text, PsycINFO, and Embase, from 2013 to 2023. Keywords including "cancer patients," "pain," "self-management," "mHealth applications," and relevant synonyms were used in the search. The Johns Hopkins research evidence appraisal tool was used to evaluate the quality of eligible studies. A narrative synthesis was conducted to analyze the extracted data.

Results:  A total of 20 studies were included, with the overall quality rated as high (n=15) to good (n=5). Using mHealth apps to monitor and manage pain was acceptable for most patients with cancer. The internal consistency of the mHealth in measuring pain was 0.96. The reported daily assessment or engagement rate ranged from 61.9% to 76.8%. All mHealth apps were designed for multimodal interventions. Participants generally had positive experiences using pain apps, rating them as enjoyable and user-friendly. In addition, 6 studies reported significant improvements in health outcomes, including enhancement in pain remission (severity and intensity), medication adherence, and a reduced frequency of breakthrough pain. The most frequently highlighted roles of mHealth apps included pain monitoring, tracking, reminders, education facilitation, and support coordination.

Conclusions:  mHealth apps are effective and acceptable in supporting pain self-management. They offer a promising multi-model approach for patients to monitor, track, and manage their pain. These findings provide evidence-based insights for leveraging mHealth apps to support cancer pain self-management. More high-quality studies are needed to examine the effectiveness of digital technology-based interventions for cancer pain self-management and to identify the facilitators and barriers to their implementation in real-world practice.

背景: 癌症疼痛在整个存活期内仍然非常普遍和顽固,因此研究利用移动医疗(mHealth)应用程序的先进功能来增强个人自我管理疼痛的能力至关重要: 本综述旨在全面了解移动医疗应用程序在支持癌症疼痛自我管理方面的可接受性、用户体验和有效性: 我们按照 Souza、Whittemore 和 Knafl 的 6 项综述流程进行了综合综述。我们在 PubMed、Scopus、CINAHL Plus with Full Text、PsycINFO 和 Embase 中检索了 2013 年至 2023 年的文献。搜索关键词包括 "癌症患者"、"疼痛"、"自我管理"、"移动医疗应用 "及相关同义词。使用约翰霍普金斯研究证据评估工具对符合条件的研究进行质量评估。对提取的数据进行了叙述性综合分析: 共纳入 20 项研究,总体质量被评为高(15 项)至良好(5 项)。对于大多数癌症患者来说,使用移动医疗应用程序监测和管理疼痛是可以接受的。移动医疗在测量疼痛方面的内部一致性为 0.96。报告的每日评估或参与率从 61.9% 到 76.8% 不等。所有移动医疗应用程序都是为多模式干预而设计的。参与者普遍对使用疼痛应用程序有积极的体验,认为这些应用程序令人愉悦且易于使用。此外,有 6 项研究报告了健康结果的显著改善,包括疼痛缓解(严重程度和强度)的增强、药物治疗的依从性以及突破性疼痛频率的降低。最常强调的移动医疗应用程序的作用包括疼痛监测、跟踪、提醒、教育促进和支持协调。它们为患者监测、跟踪和管理疼痛提供了一种有前景的多模式方法。这些发现为利用移动医疗应用程序支持癌症疼痛自我管理提供了循证见解。还需要进行更多高质量的研究,以检查基于数字技术的癌痛自我管理干预措施的有效性,并确定其在实际应用中的促进因素和障碍。
{"title":"Acceptability, Effectiveness, and Roles of mHealth Applications in Supporting Cancer Pain Self-Management: Integrative Review.","authors":"Weizi Wu, Teresa Graziano, Andrew Salner, Ming-Hui Chen, Michelle P Judge, Xiaomei Cong, Wanli Xu","doi":"10.2196/53652","DOIUrl":"10.2196/53652","url":null,"abstract":"<p><strong>Background: </strong> Cancer pain remains highly prevalent and persistent throughout survivorship, and it is crucial to investigate the potential of leveraging the advanced features of mobile health (mHealth) apps to empower individuals to self-manage their pain.</p><p><strong>Objective: </strong> This review aims to comprehensively understand the acceptability, users' experiences, and effectiveness of mHealth apps in supporting cancer pain self-management.</p><p><strong>Methods: </strong> We conducted an integrative review following Souza and Whittemore and Knafl's 6 review processes. Literature was searched in PubMed, Scopus, CINAHL Plus with Full Text, PsycINFO, and Embase, from 2013 to 2023. Keywords including \"cancer patients,\" \"pain,\" \"self-management,\" \"mHealth applications,\" and relevant synonyms were used in the search. The Johns Hopkins research evidence appraisal tool was used to evaluate the quality of eligible studies. A narrative synthesis was conducted to analyze the extracted data.</p><p><strong>Results: </strong> A total of 20 studies were included, with the overall quality rated as high (n=15) to good (n=5). Using mHealth apps to monitor and manage pain was acceptable for most patients with cancer. The internal consistency of the mHealth in measuring pain was 0.96. The reported daily assessment or engagement rate ranged from 61.9% to 76.8%. All mHealth apps were designed for multimodal interventions. Participants generally had positive experiences using pain apps, rating them as enjoyable and user-friendly. In addition, 6 studies reported significant improvements in health outcomes, including enhancement in pain remission (severity and intensity), medication adherence, and a reduced frequency of breakthrough pain. The most frequently highlighted roles of mHealth apps included pain monitoring, tracking, reminders, education facilitation, and support coordination.</p><p><strong>Conclusions: </strong> mHealth apps are effective and acceptable in supporting pain self-management. They offer a promising multi-model approach for patients to monitor, track, and manage their pain. These findings provide evidence-based insights for leveraging mHealth apps to support cancer pain self-management. More high-quality studies are needed to examine the effectiveness of digital technology-based interventions for cancer pain self-management and to identify the facilitators and barriers to their implementation in real-world practice.</p>","PeriodicalId":14756,"journal":{"name":"JMIR mHealth and uHealth","volume":"12 ","pages":"e53652"},"PeriodicalIF":5.4,"publicationDate":"2024-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11294773/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141723678","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
The Impact of User Engagement With Exposure Components on Posttraumatic Stress Symptoms in an mHealth Mobile App: Secondary Analysis of a Randomized Controlled Trial. 用户参与暴露组件对移动医疗应用程序中创伤后应激症状的影响:随机对照试验的二次分析。
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-07-18 DOI: 10.2196/49393
C Adrian Davis, Madeleine Miller, Carmen P McLean
<p><strong>Background: </strong>Mobile mental health apps are a cost-effective option for managing mental health problems, such as posttraumatic stress disorder (PTSD). The efficacy of mobile health (mHealth) apps depends on engagement with the app, but few studies have examined how users engage with different features of mHealth apps for PTSD.</p><p><strong>Objective: </strong>This study aims to examine the relationship between app engagement indices and PTSD symptom reduction using data from an unblinded pilot randomized controlled trial of "Renew" (Vertical Design), an exposure-based app for PTSD with and without coaching support. Because exposure is an effective approach for treating PTSD, we expected that engagement with exposure activities would be positively related to symptom reduction, over and above overall app usage.</p><p><strong>Methods: </strong>Participants were veterans (N=69) with clinically significant PTSD symptoms who were recruited online using Facebook advertisements and invited to use the Renew app as often as they wanted over a 6-week period. Participants completed screening and assessments online but provided informed consent, toured the app, and completed feedback interviews via telephone. We assessed users' self-reported PTSD symptoms before and after a 6-week intervention period and collected app usage data using a research-instrumented dashboard. To examine overall app engagement, we used data on the total time spent in the app, the number of log-in days, and the number of points that the user gained in the app. To examine engagement with exposure components, we used data on total time spent completing exposure activities (both in vivo and imaginal), the number of in vivo exposure activities completed, and the number of characters written in response to imaginal exposure prompts. We used hierarchical regression analyses to test the effect of engagement indices on change in PTSD symptoms.</p><p><strong>Results: </strong>Usage varied widely. Participants spent an average of 166.09 (SD 156.52) minutes using Renew, over an average of 14.7 (SD 10.71) mean log-in days. Engagement with the exposure components of the app was positively associated with PTSD symptom reduction (F6,62=2.31; P=.04). Moreover, this relationship remained significant when controlling for overall engagement with the app (ΔF3,62=4.42; P=.007). The number of characters written during imaginal exposure (β=.37; P=.009) and the amount of time spent completing exposure activities (β=.36; P=.03) were significant contributors to the model.</p><p><strong>Conclusions: </strong>To our knowledge, this is the first study to show a relationship between symptom improvement and engagement with the active therapeutic components of an mHealth app (ie, exposure) for PTSD. This relationship held when controlling for overall app use, which suggests that it was engagement with exposure, specifically, that was associated with symptom change. Future work to identify ways of
背景介绍移动心理健康应用程序是管理创伤后应激障碍(PTSD)等心理健康问题的一种具有成本效益的选择。移动医疗(mHealth)应用的功效取决于用户对应用的参与度,但很少有研究探讨用户如何参与创伤后应激障碍移动医疗应用的不同功能:本研究旨在利用 "Renew"(垂直设计)的非盲试点随机对照试验数据,研究应用程序参与度指数与创伤后应激障碍症状减轻之间的关系。由于暴露是治疗创伤后应激障碍的一种有效方法,我们预计,参与暴露活动将与症状减轻呈正相关,超过应用程序的总体使用情况:方法:参与者均为有明显创伤后应激障碍临床症状的退伍军人(69 人),他们是通过 Facebook 广告在线招募的,并被邀请在 6 周内尽可能频繁地使用 Renew 应用程序。参与者在线完成筛查和评估,但要提供知情同意书,参观应用程序,并通过电话完成反馈访谈。在为期 6 周的干预期前后,我们对用户自我报告的创伤后应激障碍症状进行了评估,并使用研究仪器仪表板收集了应用程序的使用数据。为了考察应用程序的整体参与度,我们使用了用户在应用程序中花费的总时间、登录天数以及在应用程序中获得的点数等数据。为了考察用户对曝光组件的参与度,我们使用了完成曝光活动(包括体内和意象)所花费的总时间、完成的体内曝光活动数量以及根据意象曝光提示所书写的字符数等数据。我们使用分层回归分析来检验参与指数对创伤后应激障碍症状变化的影响:使用情况差异很大。参与者使用《Renew》的平均时间为 166.09 分钟(标准差为 156.52 分钟),平均登录天数为 14.7 天(标准差为 10.71 天)。参与该应用程序的暴露部分与创伤后应激障碍症状的减轻呈正相关(F6,62=2.31;P=.04)。此外,在控制对应用程序的总体参与度后,这种关系仍然显著(ΔF3,62=4.42;P=.007)。在意象暴露过程中书写的字符数(β=.37;P=.009)和完成暴露活动所花费的时间(β=.36;P=.03)对模型有显著贡献:据我们所知,这是第一项显示症状改善与参与创伤后应激障碍移动医疗应用程序的积极治疗内容(即暴露)之间存在关系的研究。在控制应用程序的总体使用情况后,这种关系依然存在,这表明参与暴露治疗与症状改变之间存在关联。未来的工作是确定如何促进更多的人参与自我指导的暴露,这可能有助于提高移动医疗应用程序治疗创伤后应激障碍的效果。
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引用次数: 0
Wearable Data From Subjects Playing Super Mario, Taking University Exams, or Performing Physical Exercise Help Detect Acute Mood Disorder Episodes via Self-Supervised Learning: Prospective, Exploratory, Observational Study. 来自玩超级马里奥、参加大学考试或进行体育锻炼的受试者的可穿戴数据有助于通过自我监督学习检测急性情绪障碍发作:前瞻性、探索性、观察性研究。
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-07-17 DOI: 10.2196/55094
Filippo Corponi, Bryan M Li, Gerard Anmella, Clàudia Valenzuela-Pascual, Ariadna Mas, Isabella Pacchiarotti, Marc Valentí, Iria Grande, Antoni Benabarre, Marina Garriga, Eduard Vieta, Allan H Young, Stephen M Lawrie, Heather C Whalley, Diego Hidalgo-Mazzei, Antonio Vergari

Background: Personal sensing, leveraging data passively and near-continuously collected with wearables from patients in their ecological environment, is a promising paradigm to monitor mood disorders (MDs), a major determinant of the worldwide disease burden. However, collecting and annotating wearable data is resource intensive. Studies of this kind can thus typically afford to recruit only a few dozen patients. This constitutes one of the major obstacles to applying modern supervised machine learning techniques to MD detection.

Objective: In this paper, we overcame this data bottleneck and advanced the detection of acute MD episodes from wearables' data on the back of recent advances in self-supervised learning (SSL). This approach leverages unlabeled data to learn representations during pretraining, subsequently exploited for a supervised task.

Methods: We collected open access data sets recording with the Empatica E4 wristband spanning different, unrelated to MD monitoring, personal sensing tasks-from emotion recognition in Super Mario players to stress detection in undergraduates-and devised a preprocessing pipeline performing on-/off-body detection, sleep/wake detection, segmentation, and (optionally) feature extraction. With 161 E4-recorded subjects, we introduced E4SelfLearning, the largest-to-date open access collection, and its preprocessing pipeline. We developed a novel E4-tailored transformer (E4mer) architecture, serving as the blueprint for both SSL and fully supervised learning; we assessed whether and under which conditions self-supervised pretraining led to an improvement over fully supervised baselines (ie, the fully supervised E4mer and pre-deep learning algorithms) in detecting acute MD episodes from recording segments taken in 64 (n=32, 50%, acute, n=32, 50%, stable) patients.

Results: SSL significantly outperformed fully supervised pipelines using either our novel E4mer or extreme gradient boosting (XGBoost): n=3353 (81.23%) against n=3110 (75.35%; E4mer) and n=2973 (72.02%; XGBoost) correctly classified recording segments from a total of 4128 segments. SSL performance was strongly associated with the specific surrogate task used for pretraining, as well as with unlabeled data availability.

Conclusions: We showed that SSL, a paradigm where a model is pretrained on unlabeled data with no need for human annotations before deployment on the supervised target task of interest, helps overcome the annotation bottleneck; the choice of the pretraining surrogate task and the size of unlabeled data for pretraining are key determinants of SSL success. We introduced E4mer, which can be used for SSL, and shared the E4SelfLearning collection, along with its preprocessing pipeline, which can foster and expedite future research into SSL for personal sensing.

背景:利用可穿戴设备从患者生态环境中被动和近乎持续地收集到的数据进行个人传感,是监测情绪障碍(MDs)的一种很有前途的模式,而情绪障碍是全球疾病负担的一个主要决定因素。然而,收集和注释可穿戴设备数据需要耗费大量资源。因此,此类研究通常只能招募几十名患者。这成为将现代监督机器学习技术应用于 MD 检测的主要障碍之一:在本文中,我们克服了这一数据瓶颈,并以自我监督学习(SSL)的最新进展为基础,推进了从可穿戴设备数据中检测急性心肌梗死发作的工作。这种方法在预训练过程中利用未标记数据学习表征,随后在监督任务中加以利用:我们收集了使用 Empatica E4 腕带记录的开放存取数据集,这些数据集跨越了不同的、与 MD 监测无关的个人传感任务--从超级马里奥玩家的情绪识别到大学生的压力检测--并设计了一个预处理管道,用于进行身体开/关检测、睡眠/觉醒检测、分割和(可选)特征提取。通过 161 个 E4 记录对象,我们推出了迄今为止最大的开放式 E4SelfLearning 及其预处理管道。我们开发了一种新颖的 E4 定制转换器(E4mer)架构,作为 SSL 和完全监督学习的蓝图;我们评估了自监督预训练是否以及在哪些条件下,在从 64 名患者(n=32,50%,急性;n=32,50%,稳定)的记录片段中检测急性 MD 发作方面,比完全监督基线(即完全监督的 E4mer 和预深度学习算法)有所改进:SSL的表现明显优于使用我们的新型E4mer或极端梯度提升算法(XGBoost)的完全监督管道:在总共4128个记录片段中,正确分类了3353个(81.23%),而E4mer为3110个(75.35%),XGBoost为2973个(72.02%)。SSL 的表现与用于预训练的特定代用任务以及未标记数据的可用性密切相关:我们的研究表明,SSL--一种不需要人工标注就能在无标注数据上对模型进行预训练的模式--有助于克服标注瓶颈;预训练代用任务的选择和用于预训练的无标注数据的大小是决定 SSL 成功与否的关键因素。我们介绍了可用于 SSL 的 E4mer,并分享了 E4SelfLearning 套件及其预处理管道,这可以促进和加快个人传感 SSL 的未来研究。
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引用次数: 0
Deconstructing Fitbit to Specify the Effective Features in Promoting Physical Activity Among Inactive Adults: Pilot Randomized Controlled Trial. 解构 Fitbit,明确促进非活跃成年人体育锻炼的有效功能:试点随机对照试验。
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-07-12 DOI: 10.2196/51216
Keisuke Takano, Takeyuki Oba, Kentaro Katahira, Kenta Kimura

Background: Wearable activity trackers have become key players in mobile health practice as they offer various behavior change techniques (BCTs) to help improve physical activity (PA). Typically, multiple BCTs are implemented simultaneously in a device, making it difficult to identify which BCTs specifically improve PA.

Objective: We investigated the effects of BCTs implemented on a smartwatch, the Fitbit, to determine how each technique promoted PA.

Methods: This study was a single-blind, pilot randomized controlled trial, in which 70 adults (n=44, 63% women; mean age 40.5, SD 12.56 years; closed user group) were allocated to 1 of 3 BCT conditions: self-monitoring (feedback on participants' own steps), goal setting (providing daily step goals), and social comparison (displaying daily steps achieved by peers). Each intervention lasted for 4 weeks (fully automated), during which participants wore a Fitbit and responded to day-to-day questionnaires regarding motivation. At pre- and postintervention time points (in-person sessions), levels and readiness for PA as well as different aspects of motivation were assessed.

Results: Participants showed excellent adherence (mean valid-wear time of Fitbit=26.43/28 days, 94%), and no dropout was recorded. No significant changes were found in self-reported total PA (dz<0.28, P=.40 for the self-monitoring group, P=.58 for the goal setting group, and P=.19 for the social comparison group). Fitbit-assessed step count during the intervention period was slightly higher in the goal setting and social comparison groups than in the self-monitoring group, although the effects did not reach statistical significance (P=.052 and P=.06). However, more than half (27/46, 59%) of the participants in the precontemplation stage reported progress to a higher stage across the 3 conditions. Additionally, significant increases were detected for several aspects of motivation (ie, integrated and external regulation), and significant group differences were identified for the day-to-day changes in external regulation; that is, the self-monitoring group showed a significantly larger increase in the sense of pressure and tension (as part of external regulation) than the goal setting group (P=.04).

Conclusions: Fitbit-implemented BCTs promote readiness and motivation for PA, although their effects on PA levels are marginal. The BCT-specific effects were unclear, but preliminary evidence showed that self-monitoring alone may be perceived demanding. Combining self-monitoring with another BCT (or goal setting, at least) may be important for enhancing continuous engagement in PA.

Trial registration: Open Science Framework; https://osf.io/87qnb/?view_only=f7b72d48bb5044eca4b8ce729f6b403b.

背景:可穿戴活动追踪器已成为移动健康实践中的关键角色,因为它们提供了各种行为改变技术(BCT),有助于改善身体活动(PA)。通常情况下,一个设备会同时采用多种行为改变技术,因此很难确定哪些行为改变技术能具体改善体育锻炼:我们调查了在智能手表 Fitbit 上实施 BCT 的效果,以确定每种技术如何促进 PA:这项研究是一项单盲、试验性随机对照试验,70 名成年人(n=44,63% 为女性;平均年龄 40.5 岁,SD 12.56 岁;封闭用户组)被分配到 3 种 BCT 条件中的一种:自我监测(对参与者自身步数的反馈)、目标设定(提供每日步数目标)和社交比较(显示同龄人的每日步数)。每种干预都持续 4 周(全自动),在此期间,参与者佩戴 Fitbit 并回答有关动机的日常问卷。在干预前和干预后的时间点(面对面课程),对参与者的运动水平和准备情况以及动机的不同方面进行了评估:结果:参与者表现出了很好的坚持性(Fitbit 的平均有效佩戴时间=26.43/28 天,94%),没有出现辍学现象。自我报告的总运动量(dzConclusions:Fitbit实施的BCT促进了PA的准备和动机,尽管其对PA水平的影响微乎其微。BCT的具体效果尚不清楚,但初步证据表明,仅靠自我监测可能会让人感觉到要求很高。将自我监控与另一种BCT(或至少是目标设定)相结合可能对提高持续参与PA很重要:开放科学框架;https://osf.io/87qnb/?view_only=f7b72d48bb5044eca4b8ce729f6b403b。
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引用次数: 0
Impact of Remote Blood Pressure Monitoring Device Connectivity on Engagement Among Pregnant Individuals Enrolled in the Delfina Care Platform: Observational Study 远程血压监测设备连接性对加入 Delfina 护理平台的孕妇参与度的影响:观察研究
IF 5 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-07-12 DOI: 10.2196/55617
Mia Charifson, Timothy Wen, Bonnie Zell, Priyanka Vaidya, Cynthia I Rios, C Funsho Fagbohun, Isabel Fulcher
Background: Patient engagement with remote blood pressure monitoring during pregnancy is critical to optimize the associated benefits of blood pressure control and early detection. Objective: The goal of this study was to compare patient engagement and adherence to RBPM between connected and unconnected BP device users from a prospective pregnancy cohort. Methods: We compared patient engagement with and adherence to remote patient blood pressure monitoring between patients who received a connected and unconnected blood pressure device. Results: Patients with connected devices entered more blood pressure entries and had higher adherence to the remote monitoring protocols compared to patients with unconnected devices. Conclusions: In our study population of pregnant people, we found that “connected” blood pressure cuffs, which automatically sync measures to a monitoring platform or health record, increased adherence to remote monitoring protocols when compared to “unconnected” cuffs that require manual entry of measures.
背景:孕期患者参与远程血压监测对于优化血压控制和早期检测的相关益处至关重要。研究目的本研究旨在比较前瞻性妊娠队列中已连接和未连接血压设备用户的患者参与度和对远程血压监测的依从性。方法我们比较了接受联网和未联网血压设备的患者对远程患者血压监测的参与度和依从性。结果与使用未连接设备的患者相比,使用连接设备的患者输入的血压条目更多,对远程监控协议的依从性更高。结论在我们的孕妇研究人群中,我们发现与需要手动输入血压数据的 "未连接 "血压袖带相比,"连接 "血压袖带能自动将血压数据同步到监测平台或健康记录,从而提高了患者对远程监测方案的依从性。
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引用次数: 0
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JMIR mHealth and uHealth
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