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Technology-Based Music Interventions to Reduce Anxiety and Pain Among Patients Undergoing Surgery or Procedures: Systematic Review of the Literature. 以技术为基础的音乐干预,减轻手术或程序患者的焦虑和疼痛:系统性文献综述。
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-07-08 DOI: 10.2196/48802
Sunghee Park, Sohye Lee, Sheri Howard, Jeeseon Yi

Background: Hospitalized patients undergoing surgery or procedures may experience negative symptoms. Music is a nonpharmacological complementary approach and is used as an intervention to reduce anxiety, stress, and pain in these patients. Recently, music has been used conveniently in clinical situations with technology devices, and the mode of providing music is an important factor in technology-based music interventions. However, many reviews have focused only on the effectiveness of music interventions.

Objective: We aimed to review randomized controlled trials (RCTs) of technology-based music interventions for reducing anxiety and pain among patients undergoing surgery or procedures. We examined the clinical situation, devices used, delivery methods, and effectiveness of technology-based music interventions in primary articles.

Methods: The search was performed in the following 5 electronic databases: PubMed, MEDLINE (OvidSP), CINAHL complete, PSYCINFO, and Embase. This systematic review focused on technology-based music interventions. The following articles were included: (1) RCTs, (2) studies using interactive technology (eg, smartphones, mHealth, tablets, applications, and virtual reality), (3) empirical studies reporting pain and anxiety outcomes, and (4) English articles published from 2018 to 2023 (as of January 18, 2023). The risk of bias was assessed using the Cochrane Risk of Bias tool version 2.

Results: Among 292 studies identified, 21 met the inclusion criteria and were included. Of these studies, 9 reported that anxiety scores decreased after music interventions and 7 reported that pain could be decreased before, during, and after procedures. The methodology of the music intervention was important to the results on anxiety and pain in the clinical trials. More than 50% (13/21, 62%) of the studies included in this review allowed participants to select themes themselves. However, it was difficult to distinguish differences in effects depending on the device or software used for the music interventions.

Conclusions: Technology-based music interventions could help reduce anxiety and pain among patients undergoing surgery or procedures. The findings of this review could help medical teams to choose a practical methodology for music interventions. Future studies should examine the effects of advanced technology-based music interventions using smart devices and software that promote interactions between medical staff and patients.

背景:接受手术或程序的住院病人可能会出现负面症状。音乐是一种非药物的辅助方法,可用于减轻这些患者的焦虑、压力和疼痛。最近,音乐已被方便地应用于临床情况下的技术设备,而提供音乐的模式是基于技术的音乐干预的一个重要因素。然而,许多综述仅关注音乐干预的有效性:我们的目的是对基于技术的音乐干预用于减轻接受手术或程序的患者的焦虑和疼痛的随机对照试验(RCT)进行回顾。我们考察了主要文章中基于技术的音乐干预的临床情况、使用的设备、实施方法和有效性:在以下 5 个电子数据库中进行了检索:方法:在以下 5 个电子数据库中进行了检索:PubMed、MEDLINE (OvidSP)、CINAHL complete、PSYCINFO 和 Embase。本系统性综述的重点是基于技术的音乐干预。纳入了以下文章:(1)RCT;(2)使用交互式技术(如智能手机、移动医疗、平板电脑、应用程序和虚拟现实)的研究;(3)报告疼痛和焦虑结果的实证研究;(4)2018 年至 2023 年(截至 2023 年 1 月 18 日)发表的英文文章。使用 Cochrane Risk of Bias 工具 2.0 版对偏倚风险进行了评估:在确定的 292 项研究中,有 21 项符合纳入标准并被纳入。在这些研究中,9 项报告称音乐干预后焦虑评分降低,7 项报告称手术前、手术中和手术后疼痛减轻。音乐干预的方法对临床试验中焦虑和疼痛的结果非常重要。在本综述所包含的研究中,超过 50%(13/21,62%)的研究允许参与者自己选择主题。然而,很难根据音乐干预所使用的设备或软件来区分效果的差异:结论:基于技术的音乐干预有助于减轻接受手术或程序的患者的焦虑和疼痛。本综述的研究结果有助于医疗团队选择实用的音乐干预方法。未来的研究应考察使用智能设备和软件促进医务人员与患者之间互动的先进技术型音乐干预的效果。
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引用次数: 0
Assessment of Heat Exposure and Health Outcomes in Rural Populations of Western Kenya by Using Wearable Devices: Observational Case Study. 使用可穿戴设备评估肯尼亚西部农村人口的热暴露和健康结果:观察性案例研究。
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-07-04 DOI: 10.2196/54669
Ina Matzke, Sophie Huhn, Mara Koch, Martina Anna Maggioni, Stephen Munga, Julius Okoth Muma, Collins Ochieng Odhiambo, Daniel Kwaro, David Obor, Till Bärnighausen, Peter Dambach, Sandra Barteit
<p><strong>Background: </strong>Climate change increasingly impacts health, particularly of rural populations in sub-Saharan Africa due to their limited resources for adaptation. Understanding these impacts remains a challenge, as continuous monitoring of vital signs in such populations is limited. Wearable devices (wearables) present a viable approach to studying these impacts on human health in real time.</p><p><strong>Objective: </strong>The aim of this study was to assess the feasibility and effectiveness of consumer-grade wearables in measuring the health impacts of weather exposure on physiological responses (including activity, heart rate, body shell temperature, and sleep) of rural populations in western Kenya and to identify the health impacts associated with the weather exposures.</p><p><strong>Methods: </strong>We conducted an observational case study in western Kenya by utilizing wearables over a 3-week period to continuously monitor various health metrics such as step count, sleep patterns, heart rate, and body shell temperature. Additionally, a local weather station provided detailed data on environmental conditions such as rainfall and heat, with measurements taken every 15 minutes.</p><p><strong>Results: </strong>Our cohort comprised 83 participants (42 women and 41 men), with an average age of 33 years. We observed a positive correlation between step count and maximum wet bulb globe temperature (estimate 0.06, SE 0.02; P=.008). Although there was a negative correlation between minimum nighttime temperatures and heat index with sleep duration, these were not statistically significant. No significant correlations were found in other applied models. A cautionary heat index level was recorded on 194 (95.1%) of 204 days. Heavy rainfall (>20 mm/day) occurred on 16 (7.8%) out of 204 days. Despite 10 (21%) out of 47 devices failing, data completeness was high for sleep and step count (mean 82.6%, SD 21.3% and mean 86.1%, SD 18.9%, respectively), but low for heart rate (mean 7%, SD 14%), with adult women showing significantly higher data completeness for heart rate than men (2-sided t test: P=.003; Mann-Whitney U test: P=.001). Body shell temperature data achieved 36.2% (SD 24.5%) completeness.</p><p><strong>Conclusions: </strong>Our study provides a nuanced understanding of the health impacts of weather exposures in rural Kenya. Our study's application of wearables reveals a significant correlation between physical activity levels and high temperature stress, contrasting with other studies suggesting decreased activity in hotter conditions. This discrepancy invites further investigation into the unique socioenvironmental dynamics at play, particularly in sub-Saharan African contexts. Moreover, the nonsignificant trends observed in sleep disruption due to heat expose the need for localized climate change mitigation strategies, considering the vital role of sleep in health. These findings emphasize the need for context-specific research to
背景:气候变化对健康的影响越来越大,尤其是撒哈拉以南非洲的农村人口,因为他们用于适应气候变化的资源有限。了解这些影响仍是一项挑战,因为对这些人群生命体征的连续监测十分有限。可穿戴设备(可穿戴设备)为实时研究这些变化对人类健康的影响提供了一种可行的方法:本研究旨在评估消费级可穿戴设备在测量天气暴露对肯尼亚西部农村人口生理反应(包括活动、心率、体表温度和睡眠)的健康影响方面的可行性和有效性,并确定与天气暴露相关的健康影响:我们在肯尼亚西部开展了一项观察性案例研究,利用可穿戴设备在 3 周内持续监测各种健康指标,如步数、睡眠模式、心率和体表温度。此外,当地的气象站提供了降雨和高温等环境条件的详细数据,每 15 分钟测量一次:我们的团队由 83 名参与者组成(42 名女性和 41 名男性),平均年龄为 33 岁。我们观察到步数与最大湿球温度之间存在正相关(估计值 0.06,SE 0.02;P=.008)。虽然夜间最低温度和热指数与睡眠时间呈负相关,但在统计学上并不显著。在其他应用模型中也没有发现明显的相关性。在 204 天中,有 194 天(95.1%)的热指数达到警戒水平。在 204 天中,有 16 天(7.8%)出现暴雨(>20 毫米/天)。尽管 47 台设备中有 10 台(21%)出现故障,但睡眠和步数数据的完整率较高(分别为平均 82.6%,标准差 21.3% 和平均 86.1%,标准差 18.9%),而心率数据的完整率较低(平均 7%,标准差 14%),其中成年女性心率数据的完整率明显高于男性(双侧 t 检验:P=.003;曼-惠特尼 U 检验:P=.001)。体表温度数据的完整率为 36.2%(标准差为 24.5%):我们的研究让人们对肯尼亚农村地区天气暴露对健康的影响有了细致的了解。我们的研究应用可穿戴设备揭示了体力活动水平与高温压力之间的显著相关性,这与其他研究表明在较热条件下活动减少形成了鲜明对比。这种差异需要进一步研究其独特的社会环境动态,尤其是在撒哈拉以南非洲地区。此外,考虑到睡眠对健康的重要作用,在高温对睡眠的干扰方面观察到的非显著趋势表明,需要制定本地化的气候变化减缓战略。这些发现强调,在容易受到气候变化对健康的不利影响的地区,需要针对具体情况开展研究,为政策和实践提供信息。
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引用次数: 0
mHealth Apps for Dementia, Alzheimer Disease, and Other Neurocognitive Disorders: Systematic Search and Environmental Scan. 痴呆症、阿尔茨海默病和其他神经认知障碍的移动医疗应用程序:系统搜索与环境扫描
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-07-03 DOI: 10.2196/50186
Suad Ali, Hira Alizai, Delal Jemal Hagos, Sindy Ramos Rubio, Dale Calabia, Penelope Serrano Jimenez, Vinuu Aarif Senthil, Lora Appel

Background: Lifestyle behaviors including exercise, sleep, diet, stress, mental stimulation, and social interaction significantly impact the likelihood of developing dementia. Mobile health (mHealth) apps have been valuable tools in addressing these lifestyle behaviors for general health and well-being, and there is growing recognition of their potential use for brain health and dementia prevention. Effective apps must be evidence-based and safeguard user data, addressing gaps in the current state of dementia-related mHealth apps.

Objective: This study aims to describe the scope of available apps for dementia prevention and risk factors, highlighting gaps and suggesting a path forward for future development.

Methods: A systematic search of mobile app stores, peer-reviewed literature, dementia and Alzheimer association websites, and browser searches was conducted from October 19, 2022, to November 2, 2022. A total of 1044 mHealth apps were retrieved. After screening, 152 apps met the inclusion criteria and were coded by paired, independent reviewers using an extraction framework. The framework was adapted from the Silberg scale, other scoping reviews of mHealth apps for similar populations, and background research on modifiable dementia risk factors. Coded elements included evidence-based and expert credibility, app features, lifestyle elements of focus, and privacy and security.

Results: Of the 152 apps that met the final selection criteria, 88 (57.9%) addressed modifiable lifestyle behaviors associated with reducing dementia risk. However, many of these apps (59/152, 38.8%) only addressed one lifestyle behavior, with mental stimulation being the most frequently addressed. More than half (84/152, 55.2%) scored 2 points out of 9 on the Silberg scale, with a mean score of 2.4 (SD 1.0) points. Most of the 152 apps did not disclose essential information: 120 (78.9%) did not disclose expert consultation, 125 (82.2%) did not disclose evidence-based information, 146 (96.1%) did not disclose author credentials, and 134 (88.2%) did not disclose their information sources. In addition, 105 (69.2%) apps did not disclose adherence to data privacy and security practices.

Conclusions: There is an opportunity for mHealth apps to support individuals in engaging in behaviors linked to reducing dementia risk. While there is a market for these products, there is a lack of dementia-related apps focused on multiple lifestyle behaviors. Gaps in the rigor of app development regarding evidence base, credibility, and adherence to data privacy and security standards must be addressed. Following established and validated guidelines will be necessary for dementia-related apps to be effective and advance successfully.

背景:包括运动、睡眠、饮食、压力、精神刺激和社交互动在内的生活方式行为对痴呆症的发病几率有重大影响。移动医疗(mHealth)应用程序是解决这些生活方式行为对一般健康和幸福的影响的重要工具,人们越来越认识到它们在大脑健康和痴呆症预防方面的潜在用途。有效的应用程序必须以证据为基础并保护用户数据,解决目前与痴呆症相关的移动医疗应用程序存在的差距:本研究旨在描述现有痴呆症预防和风险因素应用程序的范围,突出差距并为未来发展提出建议:从 2022 年 10 月 19 日至 2022 年 11 月 2 日,对移动应用程序商店、同行评审文献、痴呆症和阿尔茨海默氏症协会网站以及浏览器进行了系统搜索。共检索到 1044 个移动医疗应用程序。经过筛选,152 个应用程序符合纳入标准,并由配对的独立审查员使用提取框架进行编码。该框架改编自西尔伯格量表、其他针对类似人群的移动医疗应用程序的范围综述以及有关可改变的痴呆症风险因素的背景研究。编码要素包括循证和专家可信度、应用程序功能、重点生活方式要素以及隐私和安全:在符合最终选择标准的 152 款应用程序中,有 88 款(57.9%)涉及与降低痴呆症风险相关的可改变的生活方式行为。然而,其中许多应用程序(59/152,38.8%)只涉及一种生活方式行为,其中最常涉及的是精神刺激。半数以上(84/152,55.2%)的应用程序在西尔伯格量表中获得了 2 分(满分 9 分),平均得分为 2.4 分(标准差为 1.0 分)。152 个应用程序中的大多数没有披露基本信息:120款(78.9%)未公开专家咨询,125款(82.2%)未公开循证信息,146款(96.1%)未公开作者资质,134款(88.2%)未公开信息来源。此外,105 款(69.2%)应用程序未披露数据隐私和安全实践:移动医疗应用程序有机会支持个人参与与降低痴呆症风险相关的行为。虽然这些产品有一定的市场,但目前还缺乏专注于多种生活方式行为的痴呆症相关应用程序。必须解决应用程序开发在证据基础、可信度以及遵守数据隐私和安全标准等方面的不足。与痴呆症相关的应用程序要想取得成效并成功推广,就必须遵循既定的、经过验证的准则。
{"title":"mHealth Apps for Dementia, Alzheimer Disease, and Other Neurocognitive Disorders: Systematic Search and Environmental Scan.","authors":"Suad Ali, Hira Alizai, Delal Jemal Hagos, Sindy Ramos Rubio, Dale Calabia, Penelope Serrano Jimenez, Vinuu Aarif Senthil, Lora Appel","doi":"10.2196/50186","DOIUrl":"10.2196/50186","url":null,"abstract":"<p><strong>Background: </strong>Lifestyle behaviors including exercise, sleep, diet, stress, mental stimulation, and social interaction significantly impact the likelihood of developing dementia. Mobile health (mHealth) apps have been valuable tools in addressing these lifestyle behaviors for general health and well-being, and there is growing recognition of their potential use for brain health and dementia prevention. Effective apps must be evidence-based and safeguard user data, addressing gaps in the current state of dementia-related mHealth apps.</p><p><strong>Objective: </strong>This study aims to describe the scope of available apps for dementia prevention and risk factors, highlighting gaps and suggesting a path forward for future development.</p><p><strong>Methods: </strong>A systematic search of mobile app stores, peer-reviewed literature, dementia and Alzheimer association websites, and browser searches was conducted from October 19, 2022, to November 2, 2022. A total of 1044 mHealth apps were retrieved. After screening, 152 apps met the inclusion criteria and were coded by paired, independent reviewers using an extraction framework. The framework was adapted from the Silberg scale, other scoping reviews of mHealth apps for similar populations, and background research on modifiable dementia risk factors. Coded elements included evidence-based and expert credibility, app features, lifestyle elements of focus, and privacy and security.</p><p><strong>Results: </strong>Of the 152 apps that met the final selection criteria, 88 (57.9%) addressed modifiable lifestyle behaviors associated with reducing dementia risk. However, many of these apps (59/152, 38.8%) only addressed one lifestyle behavior, with mental stimulation being the most frequently addressed. More than half (84/152, 55.2%) scored 2 points out of 9 on the Silberg scale, with a mean score of 2.4 (SD 1.0) points. Most of the 152 apps did not disclose essential information: 120 (78.9%) did not disclose expert consultation, 125 (82.2%) did not disclose evidence-based information, 146 (96.1%) did not disclose author credentials, and 134 (88.2%) did not disclose their information sources. In addition, 105 (69.2%) apps did not disclose adherence to data privacy and security practices.</p><p><strong>Conclusions: </strong>There is an opportunity for mHealth apps to support individuals in engaging in behaviors linked to reducing dementia risk. While there is a market for these products, there is a lack of dementia-related apps focused on multiple lifestyle behaviors. Gaps in the rigor of app development regarding evidence base, credibility, and adherence to data privacy and security standards must be addressed. Following established and validated guidelines will be necessary for dementia-related apps to be effective and advance successfully.</p>","PeriodicalId":14756,"journal":{"name":"JMIR mHealth and uHealth","volume":"12 ","pages":"e50186"},"PeriodicalIF":5.4,"publicationDate":"2024-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11255539/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141492007","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
Effect of a Smartphone App (S-Check) on Actual and Intended Help-Seeking and Motivation to Change Methamphetamine Use Among Adult Consumers of Methamphetamine in Australia: Randomized Waitlist-Controlled Trial. 智能手机应用程序(S-Check)对澳大利亚甲基苯丙胺成人消费者实际和预期求助以及改变甲基苯丙胺使用动机的影响:随机候选对照试验》。
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-07-03 DOI: 10.2196/55663
Krista J Siefried, Florence Bascombe, Brendan Clifford, Zhixin Liu, Peter Middleton, Frances Kay-Lambkin, Jack Freestone, Daniel Herman, Michael Millard, Maureen Steele, Liam Acheson, Carl Moller, Nicky Bath, Nadine Ezard
<p><strong>Background: </strong>Interventions are required that address delays in treatment-seeking and low treatment coverage among people consuming methamphetamine.</p><p><strong>Objective: </strong>We aim to determine whether a self-administered smartphone-based intervention, the "S-Check app" can increase help-seeking and motivation to change methamphetamine use, and determine factors associated with app engagement.</p><p><strong>Methods: </strong>This study is a randomized, 28-day waitlist-controlled trial. Consenting adults residing in Australia who reported using methamphetamine at least once in the last month were eligible to download the app for free from Android or iOS app stores. Those randomized to the intervention group had immediate access to the S-Check app, the control group was wait-listed for 28 days before gaining access, and then all had access until day 56. Actual help-seeking and intention to seek help were assessed by the modified Actual Help Seeking Questionnaire (mAHSQ), modified General Help Seeking Questionnaire, and motivation to change methamphetamine use by the modified readiness ruler. χ<sup>2</sup> comparisons of the proportion of positive responses to the mAHSQ, modified General Help Seeking Questionnaire, and modified readiness ruler were conducted between the 2 groups. Logistic regression models compared the odds of actual help-seeking, intention to seek help, and motivation to change at day 28 between the 2 groups. Secondary outcomes were the most commonly accessed features of the app, methamphetamine use, feasibility and acceptability of the app, and associations between S-Check app engagement and participant demographic and methamphetamine use characteristics.</p><p><strong>Results: </strong>In total, 560 participants downloaded the app; 259 (46.3%) completed eConsent and baseline; and 84 (32.4%) provided data on day 28. Participants in the immediate access group were more likely to seek professional help (mAHSQ) at day 28 than those in the control group (n=15, 45.5% vs n=12, 23.5%; χ<sup>2</sup><sub>1</sub>=4.42, P=.04). There was no significant difference in the odds of actual help-seeking, intention to seek help, or motivation to change methamphetamine use between the 2 groups on the primary logistic regression analyses, while in the ancillary analyses, the imputed data set showed a significant difference in the odds of seeking professional help between participants in the immediate access group compared to the waitlist control group (adjusted odds ratio 2.64, 95% CI 1.19-5.83, P=.02). For participants not seeking help at baseline, each minute in the app increased the likelihood of seeking professional help by day 28 by 8% (ratio 1.08, 95% CI 1.02-1.22, P=.04). Among the intervention group, a 10-minute increase in app engagement time was associated with a decrease in days of methamphetamine use by 0.4 days (regression coefficient [β] -0.04, P=.02).</p><p><strong>Conclusions: </strong>The S-Check app is a f
背景需要采取干预措施来解决甲基苯丙胺吸食者寻求治疗延迟和治疗覆盖率低的问题:我们旨在确定一种基于智能手机的自我管理干预措施--"S-Check 应用程序 "能否提高寻求帮助的积极性和改变甲基苯丙胺使用的动机,并确定与应用程序参与相关的因素:本研究是一项为期 28 天的随机候选对照试验。居住在澳大利亚、上个月至少使用过一次甲基苯丙胺的成年人均同意从安卓或 iOS 应用商店免费下载该应用程序。被随机分配到干预组的人可以立即使用 S-Check 应用程序,对照组的人要等待 28 天才能使用,然后所有人都可以使用到第 56 天。实际求助和求助意向由修改后的实际求助问卷(mAHSQ)和修改后的一般求助问卷进行评估,改变甲基苯丙胺使用的动机由修改后的准备度标尺进行评估。逻辑回归模型比较了两组在第 28 天时实际求助、求助意向和改变动机的几率。次要结果是最常使用的应用程序功能、甲基苯丙胺使用情况、应用程序的可行性和可接受性,以及 S-Check 应用程序参与度与参与者人口统计学特征和甲基苯丙胺使用特征之间的关联:共有 560 名参与者下载了该应用程序;259 人(46.3%)完成了电子同意和基线;84 人(32.4%)提供了第 28 天的数据。与对照组相比,即时访问组的参与者在第 28 天更有可能寻求专业帮助(mAHSQ)(n=15,45.5% vs n=12,23.5%;χ21=4.42,P=.04)。在主要的逻辑回归分析中,两组之间实际寻求帮助的几率、寻求帮助的意向或改变甲基苯丙胺吸食的动机没有明显差异,而在辅助分析中,估算数据集显示,与等待名单对照组相比,立即获得帮助组的参与者寻求专业帮助的几率有明显差异(调整后的几率比为 2.64,95% CI 为 1.19-5.83,P=.02)。对于基线时未寻求帮助的参与者来说,在应用程序中每待一分钟,到第 28 天时寻求专业帮助的可能性就会增加 8%(比值比 1.08,95% CI 1.02-1.22,P=.04)。在干预组中,使用应用程序的时间每增加 10 分钟,使用甲基苯丙胺的天数就会减少 0.4 天(回归系数 [β] -0.04,P=.02):S-Check应用程序是针对澳大利亚吸食甲基苯丙胺的成年人的一种可行的低资源自控干预措施。研究损耗较高,虽然这在移动健康干预中很常见,但仍有必要对 S-Check 应用程序进行更大规模的研究:澳大利亚新西兰临床试验注册中心 ACTRN12619000534189;https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=377288&isReview=true。
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引用次数: 0
The Effect of an mHealth Self-Monitoring Intervention (MI-BP) on Blood Pressure Among Black Individuals With Uncontrolled Hypertension: Randomized Controlled Trial. 移动医疗自我监测干预(MI-BP)对高血压未得到控制的黑人血压的影响:随机对照试验
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-06-28 DOI: 10.2196/57863
Lorraine R Buis, Junhan Kim, Ananda Sen, Dongru Chen, Katee Dawood, Reema Kadri, Rachelle Muladore, Melissa Plegue, Caroline R Richardson, Zora Djuric, Candace McNaughton, David Hutton, Lionel P Robert, Sun Young Park, Phillip Levy
<p><strong>Background: </strong>Hypertension is one of the most important cardiovascular disease risk factors and affects >100 million American adults. Hypertension-related health inequities are abundant in Black communities as Black individuals are more likely to use the emergency department (ED) for chronic disease-related ambulatory care, which is strongly linked to lower blood pressure (BP) control, diminished awareness of hypertension, and adverse cardiovascular events. To reduce hypertension-related health disparities, we developed MI-BP, a culturally tailored multibehavior mobile health intervention that targeted behaviors of BP self-monitoring, physical activity, sodium intake, and medication adherence in Black individuals with uncontrolled hypertension recruited from ED and community-based settings.</p><p><strong>Objective: </strong>We sought to determine the effect of MI-BP on BP as well as secondary outcomes of physical activity, sodium intake, medication adherence, and BP control compared to enhanced usual care control at 1-year follow-up.</p><p><strong>Methods: </strong>We conducted a 1-year, 2-group randomized controlled trial of the MI-BP intervention compared to an enhanced usual care control group where participants aged 25 to 70 years received a BP cuff and hypertension-related educational materials. Participants were recruited from EDs and other community-based settings in Detroit, Michigan, where they were screened for initial eligibility and enrolled. Baseline data collection and randomization occurred approximately 2 and 4 weeks after enrollment to ensure that participants had uncontrolled hypertension and were willing to take part. Data collection visits occurred at 13, 26, 39, and 52 weeks. Outcomes of interest included BP (primary outcome) and physical activity, sodium intake, medication adherence, and BP control (secondary outcomes).</p><p><strong>Results: </strong>We obtained consent from and enrolled 869 participants in this study yet ultimately randomized 162 (18.6%) participants. At 1 year, compared to the baseline, both groups showed significant decreases in systolic BP (MI-BP group: 22.5 mm Hg decrease in average systolic BP and P<.001; control group: 24.1 mm Hg decrease and P<.001) adjusted for age and sex, with no significant differences between the groups (time-by-arm interaction: P=.99). Similar patterns where improvements were noted in both groups yet no differences were found between the groups were observed for diastolic BP, physical activity, sodium intake, medication adherence, and BP control. Large dropout rates were observed in both groups (approximately 60%).</p><p><strong>Conclusions: </strong>Overall, participants randomized to both the enhanced usual care control and MI-BP conditions experienced significant improvements in BP and other outcomes; however, differences between groups were not detected, speaking to the general benefit of proactive outreach and engagement focused on cardiometabolic risk r
背景:高血压是最重要的心血管疾病风险因素之一,影响着超过 1 亿美国成年人。在黑人社区,与高血压相关的健康不平等现象比比皆是,因为黑人更有可能使用急诊科(ED)进行与慢性疾病相关的非住院治疗,而这与血压(BP)控制较低、对高血压认识不足以及不良心血管事件密切相关。为了减少与高血压相关的健康差异,我们开发了 MI-BP,这是一种根据文化定制的多行为移动健康干预措施,针对从急诊室和社区环境中招募的未得到控制的黑人高血压患者的血压自我监测、体育锻炼、钠摄入和坚持服药等行为:我们试图确定 MI-BP 对血压的影响,以及体育锻炼、钠摄入量、服药依从性和血压控制的次要结果,并与随访 1 年的增强型常规护理控制进行比较:我们进行了一项为期 1 年的 2 组随机对照试验,将 MI-BP 干预与增强型常规护理对照组进行比较,在增强型常规护理对照组中,年龄在 25 岁至 70 岁之间的参与者均接受了血压袖带和高血压相关教育材料。参与者从密歇根州底特律市的急诊室和其他社区环境中招募,并在那里接受初步资格筛选和注册。基线数据收集和随机化大约在注册后 2 周和 4 周进行,以确保参与者的高血压未得到控制并愿意参加。数据收集访问分别在 13、26、39 和 52 周进行。相关结果包括血压(主要结果)和体力活动、钠摄入量、服药依从性和血压控制(次要结果):我们征得了 869 名参与者的同意并将他们纳入了这项研究,但最终有 162 名参与者(18.6%)接受了随机治疗。1年后,与基线相比,两组的收缩压均有显著下降(MI-BP组:平均收缩压下降22.5毫米汞柱),PConclusions组:平均收缩压下降2.5毫米汞柱):总体而言,被随机分配到加强型常规护理对照组和 MI-BP 组的参与者的血压和其他结果都有明显改善;但是,没有发现组间差异,这说明在城市居住、社会经济地位较低的黑人群体中,积极主动地开展以降低心脏代谢风险为重点的外展和参与活动具有普遍益处。研究还发现了较高的辍学率,这在与类似人群合作时也是意料之中的。今后需要开展工作,更好地了解移动医疗干预措施的参与情况,尤其是在这一人群中:ClinicalTrials.gov NCT02955537;https://clinicaltrials.gov/study/NCT02955537.International 注册报告标识符 (irrid):RR2-10.2196/12601。
{"title":"The Effect of an mHealth Self-Monitoring Intervention (MI-BP) on Blood Pressure Among Black Individuals With Uncontrolled Hypertension: Randomized Controlled Trial.","authors":"Lorraine R Buis, Junhan Kim, Ananda Sen, Dongru Chen, Katee Dawood, Reema Kadri, Rachelle Muladore, Melissa Plegue, Caroline R Richardson, Zora Djuric, Candace McNaughton, David Hutton, Lionel P Robert, Sun Young Park, Phillip Levy","doi":"10.2196/57863","DOIUrl":"10.2196/57863","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;Hypertension is one of the most important cardiovascular disease risk factors and affects &gt;100 million American adults. Hypertension-related health inequities are abundant in Black communities as Black individuals are more likely to use the emergency department (ED) for chronic disease-related ambulatory care, which is strongly linked to lower blood pressure (BP) control, diminished awareness of hypertension, and adverse cardiovascular events. To reduce hypertension-related health disparities, we developed MI-BP, a culturally tailored multibehavior mobile health intervention that targeted behaviors of BP self-monitoring, physical activity, sodium intake, and medication adherence in Black individuals with uncontrolled hypertension recruited from ED and community-based settings.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;We sought to determine the effect of MI-BP on BP as well as secondary outcomes of physical activity, sodium intake, medication adherence, and BP control compared to enhanced usual care control at 1-year follow-up.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;We conducted a 1-year, 2-group randomized controlled trial of the MI-BP intervention compared to an enhanced usual care control group where participants aged 25 to 70 years received a BP cuff and hypertension-related educational materials. Participants were recruited from EDs and other community-based settings in Detroit, Michigan, where they were screened for initial eligibility and enrolled. Baseline data collection and randomization occurred approximately 2 and 4 weeks after enrollment to ensure that participants had uncontrolled hypertension and were willing to take part. Data collection visits occurred at 13, 26, 39, and 52 weeks. Outcomes of interest included BP (primary outcome) and physical activity, sodium intake, medication adherence, and BP control (secondary outcomes).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;We obtained consent from and enrolled 869 participants in this study yet ultimately randomized 162 (18.6%) participants. At 1 year, compared to the baseline, both groups showed significant decreases in systolic BP (MI-BP group: 22.5 mm Hg decrease in average systolic BP and P&lt;.001; control group: 24.1 mm Hg decrease and P&lt;.001) adjusted for age and sex, with no significant differences between the groups (time-by-arm interaction: P=.99). Similar patterns where improvements were noted in both groups yet no differences were found between the groups were observed for diastolic BP, physical activity, sodium intake, medication adherence, and BP control. Large dropout rates were observed in both groups (approximately 60%).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;Overall, participants randomized to both the enhanced usual care control and MI-BP conditions experienced significant improvements in BP and other outcomes; however, differences between groups were not detected, speaking to the general benefit of proactive outreach and engagement focused on cardiometabolic risk r","PeriodicalId":14756,"journal":{"name":"JMIR mHealth and uHealth","volume":"12 ","pages":"e57863"},"PeriodicalIF":5.4,"publicationDate":"2024-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11245662/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141468081","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
Implementing Systematic Patient-Reported Measures for Chronic Conditions Through the Naveta Value-Based Telemedicine Initiative: Observational Retrospective Multicenter Study. 通过 NAVETA 以价值为基础的远程医疗计划,对慢性病实施系统的患者报告措施:一项观察性、回顾性和多中心研究的结果。
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-06-28 DOI: 10.2196/56196
Gabriel Mercadal-Orfila, Salvador Herrera-Pérez, Núria Piqué, Francesc Mateu-Amengual, Pedro Ventayol-Bosch, María Antonia Maestre-Fullana, Joaquín Ignacio Serrano-López de Las Hazas, Francisco Fernández-Cortés, Francesc Barceló-Sansó, Santiago Rios
<p><strong>Background: </strong>Patient-reported outcome and experience measures can play a critical role in providing patient-centered and value-based health care to a growing population of patients who are chronically ill. Value-based telemedicine platforms such as the Naveta initiative may facilitate the effective integration of these tools into health care systems.</p><p><strong>Objective: </strong>This study aims to evaluate the response rate to electronic patient-reported outcome measures (ePROMs) and electronic patient-reported experience measures (ePREMs) among patients participating in the Naveta telemedicine initiative and its correlations with sociodemographic and clinical characteristics, as well as the evolution of the response rates over time.</p><p><strong>Methods: </strong>Between January 1, 2021, and June 30, 2023, a total of 53,364 ePREMs and ePROMs for 20 chronic conditions were administered through the Naveta-Phemium platform. Descriptive statistics were used to summarize continuous and categorical variables. Differences in response rates within each sociodemographic variable were analyzed using logistic regression models, with significance assessed via chi-square and post hoc Tukey tests. Two-way ANOVA was used to examine the interaction between time interval and disease type on response rate evolution.</p><p><strong>Results: </strong>A total of 3372 patients with severe chronic diseases from 64 public hospitals in Spain participated in the Naveta health questionnaire project. The overall response rate to ePROMs and ePREMs during the first 2.5 years of the Naveta initiative was 46.12% (24,704/53,364), with a baseline rate of 53.33% (7198/13,496). Several sociodemographic factors correlated with lower response rates, including male gender, older age, lower education level, frequent alcohol use, being a student, and not being physically active. There were also significant variations in response rates among different types of chronic conditions (P<.001), with the highest rates being for respiratory (433/606, 71.5%), oncologic (200/319, 62.7%), digestive (2247/3601, 62.4%), and rheumatic diseases (7506/12,982, 57.82%) and the lowest being for HIV infection (7473/22,695, 32.93%). During the first 6 months of follow-up, the response rates decreased in all disease types, except in the case of the group of patients with oncologic disease, among whom the response rate increased up to 100% (6/6). Subsequently, the overall response rate approached baseline levels.</p><p><strong>Conclusions: </strong>Recognizing the influence of sociodemographic factors on response rates is critical to identifying barriers to participation in telemonitoring programs and ensuring inclusiveness in patient-centered health care practices. The observed decline in response rates at follow-up may be due to survey fatigue, highlighting the need for strategies to mitigate this effect. In addition, the variation in response rates across chronic conditions emphasiz
背景:在为越来越多的慢性病患者提供以患者为中心、以价值为基础的医疗保健服务方面,患者报告的结果和体验措施可以发挥至关重要的作用。基于价值的远程医疗平台(如 Naveta 计划)可促进这些工具与医疗系统的有效整合:本研究旨在评估参与 Naveta 远程医疗计划的患者对电子患者报告结果测量(ePROM)和电子患者报告体验测量(ePREM)的响应率、响应率与社会人口学和临床特征的相关性以及响应率随时间的变化情况:在 2021 年 1 月 1 日至 2023 年 6 月 30 日期间,通过 Naveta-Phemium 平台对 20 种慢性病共进行了 53364 次 ePREM 和 ePROM。描述性统计用于总结连续变量和分类变量。使用逻辑回归模型分析了每个社会人口变量中响应率的差异,并通过卡方检验和事后 Tukey 检验评估了显著性。双向方差分析用于检验时间间隔和疾病类型对应答率变化的交互作用:共有来自西班牙 64 家公立医院的 3,372 名重症慢性病患者参与了 Naveta 健康问卷调查项目。在 Naveta 计划实施的头两年半时间里,ePROM 和 ePREM 的总体回复率为 46.12%,基线回复率为 53.33%。一些社会人口因素与较低的回复率有关,包括男性、年龄较大、教育水平较低、经常饮酒、学生和不爱运动。不同类型慢性病的应答率也存在明显差异,其中呼吸系统疾病(71.45%)、肿瘤疾病(62.70%)、消化系统疾病(62.40%)和风湿病(57.82%)的应答率最高,而艾滋病毒感染者的应答率最低(32.93%)。在最初 6 个月的随访中,除肿瘤组的应答率上升至 100%外,其他疾病类型的应答率均有所下降。随后,总体应答率接近基线水平:认识到社会人口因素对应答率的影响对于识别参与远程监控项目的障碍和确保以患者为中心的医疗实践的包容性至关重要。在随访中观察到的回复率下降可能是由于调查疲劳造成的,因此需要制定策略来减轻这种影响。此外,不同慢性病患者的回复率存在差异,这也强调了针对特定患者群体定制远程监控方法的重要性:
{"title":"Implementing Systematic Patient-Reported Measures for Chronic Conditions Through the Naveta Value-Based Telemedicine Initiative: Observational Retrospective Multicenter Study.","authors":"Gabriel Mercadal-Orfila, Salvador Herrera-Pérez, Núria Piqué, Francesc Mateu-Amengual, Pedro Ventayol-Bosch, María Antonia Maestre-Fullana, Joaquín Ignacio Serrano-López de Las Hazas, Francisco Fernández-Cortés, Francesc Barceló-Sansó, Santiago Rios","doi":"10.2196/56196","DOIUrl":"10.2196/56196","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;Patient-reported outcome and experience measures can play a critical role in providing patient-centered and value-based health care to a growing population of patients who are chronically ill. Value-based telemedicine platforms such as the Naveta initiative may facilitate the effective integration of these tools into health care systems.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;This study aims to evaluate the response rate to electronic patient-reported outcome measures (ePROMs) and electronic patient-reported experience measures (ePREMs) among patients participating in the Naveta telemedicine initiative and its correlations with sociodemographic and clinical characteristics, as well as the evolution of the response rates over time.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;Between January 1, 2021, and June 30, 2023, a total of 53,364 ePREMs and ePROMs for 20 chronic conditions were administered through the Naveta-Phemium platform. Descriptive statistics were used to summarize continuous and categorical variables. Differences in response rates within each sociodemographic variable were analyzed using logistic regression models, with significance assessed via chi-square and post hoc Tukey tests. Two-way ANOVA was used to examine the interaction between time interval and disease type on response rate evolution.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;A total of 3372 patients with severe chronic diseases from 64 public hospitals in Spain participated in the Naveta health questionnaire project. The overall response rate to ePROMs and ePREMs during the first 2.5 years of the Naveta initiative was 46.12% (24,704/53,364), with a baseline rate of 53.33% (7198/13,496). Several sociodemographic factors correlated with lower response rates, including male gender, older age, lower education level, frequent alcohol use, being a student, and not being physically active. There were also significant variations in response rates among different types of chronic conditions (P&lt;.001), with the highest rates being for respiratory (433/606, 71.5%), oncologic (200/319, 62.7%), digestive (2247/3601, 62.4%), and rheumatic diseases (7506/12,982, 57.82%) and the lowest being for HIV infection (7473/22,695, 32.93%). During the first 6 months of follow-up, the response rates decreased in all disease types, except in the case of the group of patients with oncologic disease, among whom the response rate increased up to 100% (6/6). Subsequently, the overall response rate approached baseline levels.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;Recognizing the influence of sociodemographic factors on response rates is critical to identifying barriers to participation in telemonitoring programs and ensuring inclusiveness in patient-centered health care practices. The observed decline in response rates at follow-up may be due to survey fatigue, highlighting the need for strategies to mitigate this effect. In addition, the variation in response rates across chronic conditions emphasiz","PeriodicalId":14756,"journal":{"name":"JMIR mHealth and uHealth","volume":" ","pages":"e56196"},"PeriodicalIF":5.4,"publicationDate":"2024-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11245666/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140305621","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
Correction: Effects of a Planned Web-Based Educational Intervention Based on the Health Belief Model for Patients With Ischemic Stroke in Promoting Secondary Prevention During the COVID-19 Lockdown in China: Quasi-Experimental Study. 更正:基于健康信念模型的缺血性脑卒中患者计划性网络教育干预对促进中国 COVID-19 封锁期间二级预防的影响:准实验研究。
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-06-28 DOI: 10.2196/60953
Zhuo Liu, Xin Sun, Zhen-Ni Guo, Ye Sun, Yi Yang, Xiuli Yan
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引用次数: 0
Long-Term Efficacy of a Mobile Mental Wellness Program: Prospective Single-Arm Study. 移动心理健康计划的长期功效:前瞻性单臂研究
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-06-27 DOI: 10.2196/54634
Meaghan McCallum, Matthew Baldwin, Paige Thompson, Kelly Blessing, Maria Frisch, Annabell Ho, Matthew Cole Ainsworth, Ellen Siobhan Mitchell, Andreas Michaelides, Christine N May
<p><strong>Background: </strong>Rising rates of psychological distress (symptoms of depression, anxiety, and stress) among adults in the United States necessitate effective mental wellness interventions. Despite the prevalence of smartphone app-based programs, research on their efficacy is limited, with only 14% showing clinically validated evidence. Our study evaluates Noom Mood, a commercially available smartphone-based app that uses cognitive behavioral therapy and mindfulness-based programming. In this study, we address gaps in the existing literature by examining postintervention outcomes and the broader impact on mental wellness.</p><p><strong>Objective: </strong>Noom Mood is a smartphone-based mental wellness program designed to be used by the general population. This prospective study evaluates the efficacy and postintervention outcomes of Noom Mood. We aim to address the rising psychological distress among adults in the United States.</p><p><strong>Methods: </strong>A 1-arm study design was used, with participants having access to the Noom Mood program for 16 weeks (N=273). Surveys were conducted at baseline, week 4, week 8, week 12, week 16, and week 32 (16 weeks' postprogram follow-up). This study assessed a range of mental health outcomes, including anxiety symptoms, depressive symptoms, perceived stress, well-being, quality of life, coping, emotion regulation, sleep, and workplace productivity (absenteeism or presenteeism).</p><p><strong>Results: </strong>The mean age of participants was 40.5 (SD 11.7) years. Statistically significant improvements in anxiety symptoms, depressive symptoms, and perceived stress were observed by week 4 and maintained through the 16-week intervention and the 32-week follow-up. The largest changes were observed in the first 4 weeks (29% lower, 25% lower, and 15% lower for anxiety symptoms, depressive symptoms, and perceived stress, respectively), and only small improvements were observed afterward. Reductions in clinically relevant anxiety (7-item generalized anxiety disorder scale) and depression (8-item Patient Health Questionnaire depression scale) criteria were also maintained from program initiation through the 16-week intervention and the 32-week follow-up. Work productivity also showed statistically significant results, with participants gaining 2.57 productive work days from baseline at 16 weeks, and remaining relatively stable (2.23 productive work days gained) at follow-up (32 weeks). Additionally, effects across all coping, sleep disturbance (23% lower at 32 weeks), and emotion dysregulation variables exhibited positive and significant trends at all time points (15% higher, 23% lower, and 25% higher respectively at 32 weeks).</p><p><strong>Conclusions: </strong>This study contributes insights into the promising positive impact of Noom Mood on mental health and well-being outcomes, extending beyond the intervention phase. Though more rigorous studies are necessary to understand the mechanism of
背景:美国成年人的心理困扰(抑郁、焦虑和压力症状)发生率不断上升,因此有必要采取有效的心理健康干预措施。尽管基于智能手机应用程序的项目很普遍,但对其功效的研究却很有限,只有 14% 的项目显示出临床验证的证据。我们的研究对 Noom Mood 进行了评估,这是一款基于智能手机的商用应用程序,采用了认知行为疗法和正念程序。在这项研究中,我们通过考察干预后的结果以及对心理健康的广泛影响,填补了现有文献的空白:Noom Mood 是一款基于智能手机的心理健康程序,旨在供普通人群使用。这项前瞻性研究评估了 Noom Mood 的疗效和干预后的结果。我们的目标是解决美国成年人日益严重的心理困扰:研究采用单臂研究设计,参与者可参加为期 16 周的 Noom Mood 计划(N=273)。分别在基线、第 4 周、第 8 周、第 12 周、第 16 周和第 32 周(16 周计划后随访)进行调查。这项研究对一系列心理健康结果进行了评估,包括焦虑症状、抑郁症状、感知压力、幸福感、生活质量、应对能力、情绪调节、睡眠和工作效率(旷工或缺勤):参与者的平均年龄为 40.5(标准差 11.7)岁。第 4 周时,焦虑症状、抑郁症状和感知压力均有明显改善,并在 16 周的干预和 32 周的随访中保持不变。前四周的变化最大(焦虑症状、抑郁症状和压力感分别降低了 29%、25% 和 15%),之后仅有小幅改善。临床相关焦虑(7 项广泛性焦虑症量表)和抑郁(8 项患者健康问卷抑郁量表)标准的降低也从项目启动到 16 周的干预和 32 周的随访期间保持不变。工作效率也取得了显著的统计结果,在 16 周时,参与者的工作效率比基线提高了 2.57 天,在 32 周的随访中,工作效率保持相对稳定(提高了 2.23 天)。此外,所有应对、睡眠障碍(32 周时降低 23%)和情绪失调变量的效果在所有时间点都呈现出积极和显著的趋势(32 周时分别提高 15%、降低 23% 和提高 25%):这项研究有助于深入了解 Noom Mood 对心理健康和幸福结果的积极影响,这种影响有望延伸到干预阶段之后。虽然要了解其作用机制还需要更严格的研究,但这项探索性研究填补了文献中的重要空白,凸显了基于智能手机的心理健康项目在减少心理健康支持障碍和改善不同幸福感方面的潜力。未来的研究应探索此类干预措施在不同人群中的可扩展性、可行性和长期坚持性。
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引用次数: 0
A Chatbot-Delivered Stress Management Coaching for Students (MISHA App): Pilot Randomized Controlled Trial. 学生压力管理辅导聊天机器人(MISHA App):随机对照试验。
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-06-26 DOI: 10.2196/54945
Sandra Ulrich, Natascha Lienhard, Hansjörg Künzli, Tobias Kowatsch

Background: Globally, students face increasing mental health challenges, including elevated stress levels and declining well-being, leading to academic performance issues and mental health disorders. However, due to stigma and symptom underestimation, students rarely seek effective stress management solutions. Conversational agents in the health sector have shown promise in reducing stress, depression, and anxiety. Nevertheless, research on their effectiveness for students with stress remains limited.

Objective: This study aims to develop a conversational agent-delivered stress management coaching intervention for students called MISHA and to evaluate its effectiveness, engagement, and acceptance.

Methods: In an unblinded randomized controlled trial, Swiss students experiencing stress were recruited on the web. Using a 1:1 randomization ratio, participants (N=140) were allocated to either the intervention or waitlist control group. Treatment effectiveness on changes in the primary outcome, that is, perceived stress, and secondary outcomes, including depression, anxiety, psychosomatic symptoms, and active coping, were self-assessed and evaluated using ANOVA for repeated measure and general estimating equations.

Results: The per-protocol analysis revealed evidence for improvement of stress, depression, and somatic symptoms with medium effect sizes (Cohen d=-0.36 to Cohen d=-0.60), while anxiety and active coping did not change (Cohen d=-0.29 and Cohen d=0.13). In the intention-to-treat analysis, similar results were found, indicating reduced stress (β estimate=-0.13, 95% CI -0.20 to -0.05; P<.001), depressive symptoms (β estimate=-0.23, 95% CI -0.38 to -0.08; P=.003), and psychosomatic symptoms (β estimate=-0.16, 95% CI -0.27 to -0.06; P=.003), while anxiety and active coping did not change. Overall, 60% (42/70) of the participants in the intervention group completed the coaching by completing the postintervention survey. They particularly appreciated the quality, quantity, credibility, and visual representation of information. While individual customization was rated the lowest, the target group fitting was perceived as high.

Conclusions: Findings indicate that MISHA is feasible, acceptable, and effective in reducing perceived stress among students in Switzerland. Future research is needed with different populations, for example, in students with high stress levels or compared to active controls.

Trial registration: German Clinical Trials Register DRKS 00030004; https://drks.de/search/en/trial/DRKS00030004.

背景:在全球范围内,学生面临着越来越多的心理健康挑战,包括压力水平升高和幸福感下降,从而导致学习成绩问题和心理健康失调。然而,由于耻辱感和症状被低估,学生很少寻求有效的压力管理解决方案。健康领域的对话代理在减轻压力、抑郁和焦虑方面已显示出前景。然而,有关其对有压力的学生的有效性的研究仍然有限:本研究旨在为学生开发一种名为 MISHA 的会话代理压力管理辅导干预措施,并对其有效性、参与度和接受度进行评估:在一项非盲法随机对照试验中,通过网络招募了面临压力的瑞士学生。采用 1:1 的随机分配比例,将参与者(N=140)分配到干预组或候补对照组。对主要结果(即感知压力)和次要结果(包括抑郁、焦虑、心身症状和积极应对)的治疗效果进行自我评估,并使用重复测量方差分析和一般估计方程进行评价:按协议分析显示,压力、抑郁和躯体症状得到了改善,其效应大小为中等(Cohen d=-0.36 至 Cohen d=-0.60),而焦虑和积极应对没有变化(Cohen d=-0.29 和 Cohen d=0.13)。在意向治疗分析中也发现了类似的结果,表明压力有所减轻(β 估计值=-0.13,95% CI -0.20至-0.05;PC结论:研究结果表明,MISHA 在减少瑞士学生感知压力方面是可行的、可接受的和有效的。未来还需要对不同人群进行研究,例如压力水平较高的学生或与积极的对照组进行比较:德国临床试验注册 DRKS 00030004;https://drks.de/search/en/trial/DRKS00030004。
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引用次数: 0
Detection of Mild Cognitive Impairment Through Hand Motor Function Under Digital Cognitive Test: Mixed Methods Study. 通过数字认知测试下的手部运动功能检测轻度认知障碍:混合方法研究
IF 5.4 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES Pub Date : 2024-06-26 DOI: 10.2196/48777
Aoyu Li, Jingwen Li, Jiali Chai, Wei Wu, Suamn Chaudhary, Juanjuan Zhao, Yan Qiang

Background: Early detection of cognitive impairment or dementia is essential to reduce the incidence of severe neurodegenerative diseases. However, currently available diagnostic tools for detecting mild cognitive impairment (MCI) or dementia are time-consuming, expensive, or not widely accessible. Hence, exploring more effective methods to assist clinicians in detecting MCI is necessary.

Objective: In this study, we aimed to explore the feasibility and efficiency of assessing MCI through movement kinetics under tablet-based "drawing and dragging" tasks.

Methods: We iteratively designed "drawing and dragging" tasks by conducting symposiums, programming, and interviews with stakeholders (neurologists, nurses, engineers, patients with MCI, healthy older adults, and caregivers). Subsequently, stroke patterns and movement kinetics were evaluated in healthy control and MCI groups by comparing 5 categories of features related to hand motor function (ie, time, stroke, frequency, score, and sequence). Finally, user experience with the overall cognitive screening system was investigated using structured questionnaires and unstructured interviews, and their suggestions were recorded.

Results: The "drawing and dragging" tasks can detect MCI effectively, with an average accuracy of 85% (SD 2%). Using statistical comparison of movement kinetics, we discovered that the time- and score-based features are the most effective among all the features. Specifically, compared with the healthy control group, the MCI group showed a significant increase in the time they took for the hand to switch from one stroke to the next, with longer drawing times, slow dragging, and lower scores. In addition, patients with MCI had poorer decision-making strategies and visual perception of drawing sequence features, as evidenced by adding auxiliary information and losing more local details in the drawing. Feedback from user experience indicates that our system is user-friendly and facilitates screening for deficits in self-perception.

Conclusions: The tablet-based MCI detection system quantitatively assesses hand motor function in older adults and further elucidates the cognitive and behavioral decline phenomenon in patients with MCI. This innovative approach serves to identify and measure digital biomarkers associated with MCI or Alzheimer dementia, enabling the monitoring of changes in patients' executive function and visual perceptual abilities as the disease advances.

背景:早期发现认知障碍或痴呆症对于降低严重神经退行性疾病的发病率至关重要。然而,目前可用来检测轻度认知功能障碍(MCI)或痴呆症的诊断工具耗时长、价格昂贵或不能广泛使用。因此,有必要探索更有效的方法来帮助临床医生检测 MCI:在本研究中,我们旨在探索在基于平板电脑的 "绘图和拖动 "任务中通过运动动力学评估 MCI 的可行性和效率:方法:我们通过与相关人员(神经科医生、护士、工程师、MCI 患者、健康老年人和护理人员)进行座谈会、编程和访谈,反复设计了 "绘图和拖动 "任务。随后,通过比较与手部运动功能相关的 5 类特征(即时间、中风、频率、得分和顺序),对健康对照组和 MCI 组的中风模式和运动动力学进行了评估。最后,使用结构化问卷和非结构化访谈调查了用户对整个认知筛查系统的体验,并记录了他们的建议:结果:"绘图和拖动 "任务能有效检测 MCI,平均准确率为 85%(SD 2%)。通过对运动动力学的统计比较,我们发现基于时间和分数的特征是所有特征中最有效的。具体来说,与健康对照组相比,MCI 组患者的手从一个笔画切换到下一个笔画所需的时间明显增加,绘制时间更长,拖动速度更慢,得分也更低。此外,MCI 患者的决策策略和对绘图序列特征的视觉感知能力较差,表现为在绘图中添加辅助信息和丢失更多局部细节。用户体验反馈表明,我们的系统界面友好,便于筛查自我感知缺陷:基于平板电脑的 MCI 检测系统可定量评估老年人的手部运动功能,并进一步阐明 MCI 患者的认知和行为衰退现象。这种创新方法可用于识别和测量与 MCI 或阿尔茨海默痴呆症相关的数字生物标志物,从而监测患者的执行功能和视觉感知能力随着病情发展而发生的变化。
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