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Evaluation of the Implementation of a Mobile Health App to Support Dutch Primary Care for Diabetes: Qualitative Study. 对支持荷兰糖尿病初级保健的移动健康应用程序实施的评估:定性研究。
IF 3 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-02-09 DOI: 10.2196/54431
Liselot N van den Berg, Lisenka Te Lindert, Jiska J Aardoom, Anke Versluis, Sofie H Willems, Niels H Chavannes, Marise J Kasteleyn
<p><strong>Background: </strong>Over 1 million Dutch people have diabetes, of whom 90% have type 2 diabetes. Studies show that lifestyle plays an important role in the course of type 2 diabetes. MiGuide (MiGuide Ltd) is an online platform that helps people adopt and sustain lifestyle changes. The platform is integrated into existing diabetes care within primary care. Previous research has shown that implementing new (eHealth) interventions is challenging and may reduce effectiveness. Mapping out the barriers and success factors in the implementation process is essential so that eHealth interventions such as MiGuide can be used effectively in regular health care.</p><p><strong>Objective: </strong>This study aimed to evaluate the implementation of MiGuide within Dutch primary care.</p><p><strong>Methods: </strong>A qualitative study design was used, supplemented by quantitative data from patients. Five general practices participated. Three focus groups (FGs; at baseline, after 6 months, and after 12 months) were conducted with 3 general practitioners, 3 FGs with 8 specialized practice nurses (divided into 2 separate groups with 4 participants per group), 2 FGs (at 6 months and after 12 months) with 5 patients, and 2 FGs (at baseline and after 12 months) with 4 stakeholders from the management of the care group. The implementation process was discussed with health care professionals and management, and usage and user-friendliness were discussed with patients. The framework method was used to analyze the data. The following quantitative data were collected: patient characteristics, user data, and questionnaires at baseline and 6 months, assessing quality of life, usability, and diabetes self-care. The quantitative data were examined using exploratory analyses.</p><p><strong>Results: </strong>Four themes were found in the qualitative data: "innovation," "capability, motivation, and opportunity," "processes," and "setting." Different factors within these themes played an essential role throughout the implementation process, such as facilities, technical difficulties, motivation, COVID-19, and the work processes. Areas for improvement were also identified. The supplemented quantitative data showed that usability scored below average at 6 months (mean 53.8; SD 9.3; n=8). Participants had a mean score of 0.84 (SD 0.13) on the EuroQoL-5 dimension and 81.9 (SD 13.4) on the EuroQoL visual analogue scale at baseline. Moreover, the average number of days someone exercised was 4.2 (SD 1.7), and the number of days someone ate a generally healthy diet was 5.1 (SD 1.3). Insufficient data on quality of life and diabetes self-care were collected at 6 months and therefore not presented in this study.</p><p><strong>Conclusions: </strong>Implementation is a complex process with multiple barriers and facilitators. It is essential to explore the use of context-specific strategies that are aligned with the implementation process phase. Further research is needed to evalua
背景:超过100万荷兰人患有糖尿病,其中90%患有2型糖尿病。研究表明,生活方式在2型糖尿病的病程中起着重要作用。MiGuide (MiGuide Ltd)是一个帮助人们接受和维持生活方式改变的在线平台。该平台被整合到现有的初级保健糖尿病护理中。先前的研究表明,实施新的(电子卫生)干预措施具有挑战性,可能会降低有效性。确定实施过程中的障碍和成功因素至关重要,这样才能在常规卫生保健中有效地利用诸如MiGuide之类的电子卫生干预措施。目的:本研究旨在评估咪桂德在荷兰初级保健中的实施情况。方法:采用定性研究设计,辅以患者的定量资料。共有五名全科医生参与。3个焦点组(FGs,基线时、6个月后和12个月后)有3名全科医生参与,3个FGs有8名专业执业护士参与(分为2个独立组,每组4名参与者),2个FGs(6个月和12个月后)有5名患者参与,2个FGs(基线时和12个月后)有4名来自护理组管理层的利益相关者参与。与卫生保健专业人员和管理人员讨论了实施过程,并与患者讨论了使用和用户友好性。采用框架法对数据进行分析。收集以下定量数据:患者特征,用户数据,基线和6个月的问卷调查,评估生活质量,可用性和糖尿病自我护理。定量数据采用探索性分析进行检验。结果:在定性数据中发现了四个主题:“创新”,“能力,动机和机会”,“过程”和“设置”。这些主题中的不同因素在整个实施过程中发挥了至关重要的作用,例如设施、技术困难、动机、COVID-19和工作流程。还确定了需要改进的领域。补充的定量数据显示,6个月时可用性得分低于平均水平(平均53.8;SD 9.3; n=8)。参与者在基线时EuroQoL-5维度的平均得分为0.84 (SD 0.13), EuroQoL视觉模拟量表的平均得分为81.9 (SD 13.4)。此外,锻炼的平均天数为4.2天(标准差1.7),健康饮食的平均天数为5.1天(标准差1.3)。在6个月时收集的生活质量和糖尿病自我护理数据不足,因此未在本研究中提出。结论:实施是一个复杂的过程,有多种障碍和促进因素。探索与实现过程阶段相一致的特定于上下文的策略的使用是至关重要的。需要进一步的研究来评估下一个版本的MiGuide平台,该平台正在另一个有生活方式教练的环境中实施。
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引用次数: 0
Sex Representation and User Preferences in Pain Drawing Body Charts in Back Pain Research: Multimethod Study. 背痛研究中疼痛绘身图的性别表征与使用者偏好:多方法研究。
IF 3 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-02-09 DOI: 10.2196/76175
Sonja Schläpfer, Casey Murphy, Yanick X Lukic, Concepción Campos-Asensio, Giovanni Colacicco, Beatrice A Lauber, Sophie Masneuf, Luana Nyirö, Georg W Kajdi, Reto Sutter, Christoph J Laux, Philipp Ackermann, Jesús López-Alcalde, Claudia M Witt

Background: Pain drawing (PD) body charts are widely used in back pain research, but the representation of sex in these charts has not been systematically evaluated.

Objective: This study aims to evaluate sex representation in PD body charts used in back pain research, assess the perception of a newly designed sex-neutral body chart, and explore user preferences for sex representation in PD body charts.

Methods: We conducted a multimethod study comprising: (1) a scoping review to assess sex representation and the reporting of sex in PD body charts in back pain literature, (2) an expert opinion study where anatomy experts evaluated the perceived sex of extracted body charts, and (3) a survey among a representative sample of UK adults with and without back pain to assess the perception of a newly designed sex-neutral body chart and explore preferences for sex representation in PD body charts.

Results: From 349 full-text papers, 108 articles met the inclusion criteria. Most (103/108, 95.4%) did not report the sex of the body charts used, and only 5.6% (6/108) included both male and female charts. Experts showed fair to moderate agreement (Fleiss κ=0.306; Gwet AC1=0.456) in assessing the sex of charts, with most charts assessed as male based on majority ratings (59/108, 54.6%) and classified as male-biased relative to the sex distribution of study participants (76/108, 67.7%). The newly designed sex-neutral body chart was perceived as sex-neutral by 68.5% (204/298) of survey participants across diverse groups. However, perceptions varied by racial group: 73% (181/248) of White participants viewed it as sex-neutral, compared to 42.5% (17/40) of participants from smaller racial groups (χ²2=15.9; P=.001). Female participants slightly preferred female charts (85/154, 55.2%); male participants preferred sex-neutral ones (88/144, 61.1%). Nonetheless, most female participants (82/154, 53.3%) and male participants (107/144, 74.3%) considered the option to choose between male, female, and sex-neutral chart versions unimportant.

Conclusions: Our study reveals reporting gaps and a predominant male bias in the representation of sex in PD body charts used in back pain research. The newly developed sex-neutral body chart was widely perceived as sex-neutral, offering a promising step toward more inclusive pain assessment. However, variations in perception across racial groups highlight the need for cultural considerations in design. These findings underscore the potential of sex-neutral and culturally sensitive body charts to enhance the inclusivity and equity of back pain research and clinical practice.

背景:疼痛图(PD)身体图被广泛应用于背痛研究,但这些图中性别的代表性尚未得到系统的评估。目的:本研究旨在评估用于背部疼痛研究的PD身体图中的性别表征,评估新设计的性别中性身体图的感知,并探讨用户对PD身体图中性别表征的偏好。方法:我们进行了一项多重方法研究包括:(1)范围审查评估性表示和性的报道在PD身体背部疼痛文学中图表,(2)一个专家意见研究解剖学专家评估提取身体的感知性图表,和(3)的一项调查具有代表性的英国成年人有或没有背部疼痛评估新设计的感知sex-neutral身体图和探讨性的偏好表示体内PD图表。结果:349篇全文论文中,108篇符合纳入标准。大多数(103/108,95.4%)没有报告所使用的身体图的性别,只有5.6%(6/108)包括男性和女性的图表。专家在评估图表性别方面表现出公平到中等程度的一致(Fleiss κ=0.306; Gwet AC1=0.456),大多数图表根据多数评分(59/108,54.6%)被评估为男性,并根据研究参与者的性别分布(76/108,67.7%)被分类为男性偏见。68.5%(204/298)的不同群体的调查参与者认为新设计的性别中性身材图是中性的。然而,看法因种族而异:73%(181/248)的白人参与者认为它是中性的,而42.5%(17/40)的小种族参与者认为它是中性的(χ 2=15.9; P=.001)。女性参与者略微偏爱女性图表(85/154,55.2%);男性参与者更倾向于性别中立(88/144,61.1%)。尽管如此,大多数女性参与者(82/154,53.3%)和男性参与者(107/144,74.3%)认为在男性、女性和性别中立的图表版本之间进行选择并不重要。结论:我们的研究揭示了在背痛研究中使用的PD身体图中,在性别代表方面的报告差距和主要的男性偏见。新开发的性别中立的身体图表被广泛认为是性别中立的,为更包容的疼痛评估提供了有希望的一步。然而,不同种族群体的认知差异突出了在设计中考虑文化因素的必要性。这些发现强调了性别中立和文化敏感的身体图在增强背痛研究和临床实践的包容性和公平性方面的潜力。
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引用次数: 0
Development of the ERATbi App, a Clinical Decision Support System for Early Recovery After Traumatic Brain Injury in the ICU: Usability Study. 用于ICU创伤性脑损伤早期恢复的临床决策支持系统ERATbi应用程序的开发:可用性研究
IF 3 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-02-06 DOI: 10.2196/79981
Hsiao-Ching Yen, I-Hui Wu, Wei-Ling Hsiao, Sheng-Ru Lai, Chen-Hao Yang, Hsien-Chi Liao, Yin-Yi Han

Background: Early rehabilitation in neurocritical care is often underutilized due to fragmented workflows, interdisciplinary coordination challenges, and the absence of structured digital decision support. Traditional clinical decision support systems (CDSS) often address single domains and lack adaptability to the dynamic, multiprofessional workflows of intensive care units (ICUs).

Objective: To develop and evaluate the usability of the ERATbi App (Early Recovery After Traumatic Brain Injury App), a modular, tablet-based CDSS was designed to streamline early rehabilitation planning and strengthen interdisciplinary coordination for patients with moderate-to-severe traumatic brain injury (TBI) in intensive care settings.

Methods: The ERATbi app integrates four functional modules-delirium risk management, precision nutrition, stepwise early mobilization, and respiratory care for rib fractures-into a unified interface. A simulation-based usability study was conducted with 18 ICU clinicians. Evaluation metrics included System Usability Scale (SUS) scores, task completion rates, error rates, and task durations. Additional user feedback was collected via a 5-point Likert satisfaction survey and semi-structured qualitative interviews.

Results: The app demonstrated high usability (mean SUS score 83.6, SD 7.4), a 100% (18/18 participants) task completion rate, and a low error rate (4.2%). Average module completion time was 6.5 minutes, and user satisfaction was high (mean 4.7, SD 0.5). Users highlighted the value of the app's visual logic, real-time alerts, adaptive thresholds, and modular workflow integration for enhancing team coordination and decision consistency.

Conclusions: The ERATbi app demonstrated excellent usability, high user satisfaction, and clinical relevance in simulated ICU workflows. Its logic-driven, workflow- integrated design may support scalable, interdisciplinary implementation of early rehabilitation in neurocritical care settings.

背景:由于支离破碎的工作流程、跨学科的协调挑战以及缺乏结构化的数字决策支持,神经危重症护理的早期康复往往得不到充分利用。传统的临床决策支持系统(CDSS)通常处理单一领域,缺乏对重症监护病房(icu)动态、多专业工作流程的适应性。目的:为了开发和评估ERATbi应用程序(创伤性脑损伤后早期恢复应用程序)的可用性,设计了一个模块化的、基于平板电脑的CDSS,以简化重症监护室中重度创伤性脑损伤(TBI)患者的早期康复计划,加强跨学科协调。方法:ERATbi应用程序将谵妄风险管理、精准营养、分步早期活动、肋骨骨折呼吸护理四个功能模块整合到一个统一的界面中。对18名ICU临床医生进行了一项基于模拟的可用性研究。评估指标包括系统可用性量表(SUS)分数、任务完成率、错误率和任务持续时间。额外的用户反馈通过5点李克特满意度调查和半结构化定性访谈收集。结果:该应用程序显示出高可用性(平均SUS得分83.6,SD 7.4), 100%(18/18参与者)任务完成率和低错误率(4.2%)。平均模块完成时间为6.5分钟,用户满意度高(平均值4.7,标准差0.5)。用户强调了应用程序的视觉逻辑、实时警报、自适应阈值和模块化工作流集成的价值,以增强团队协调和决策一致性。结论:ERATbi应用程序在模拟ICU工作流程中表现出出色的可用性、高用户满意度和临床相关性。它的逻辑驱动,工作流集成设计可以支持可扩展的,跨学科的早期康复实施在神经危重症护理设置。
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引用次数: 0
Opportunities for Improved Device Design Based on Central Line Placement Practices: Contextual Inquiry Study. 基于中心线放置实践的改进设备设计的机会:一项上下文探究研究。
IF 3 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-02-06 DOI: 10.2196/84621
Mary Beth Privitera, Sameer Khan, Bilal Irfan, Shayan Ali, Cecelia Arredondo, Kyrsten Sanderson, Jordan Bonomo
<p><strong>Background: </strong>Central venous catheters (CVCs) are indispensable to contemporary critical care, perioperative management, and emergency resuscitation, yet their insertion remains fraught with preventable harm and inefficiency.</p><p><strong>Objective: </strong>This study aimed to identify all areas of CVC placement that can be improved through device design using human-centered design and qualitative research methods.</p><p><strong>Methods: </strong>This qualitative study was a contextual inquiry of CVC placement, which included observation alongside brief face-to-face interviews with physicians. It was aimed at providing a depth of understanding using evidence to demonstrate causality. This study was conducted at 3 hospitals in the emergency department, the intensive care unit, and the operating rooms. Where possible and with additional consent, sessions were recorded in video or still photography, or at times both. This study included 19 observations and 24 interviews.</p><p><strong>Results: </strong>In this study, the approach to CVC insertion was consistent across hospitals and care environments, with moderate variability spanning a few sections, such as suture and dressing use or lack thereof in specific care environments. The described and observed difficulties leave room for improvement in device design. The results of this study indicated that there are 34 discrete steps to placing a CVC line, with most time spent during sterile preparation. As a result of the device or kit design, challenges were observed. These included missing essential materials from kits, difficulty distinguishing between nonsterile and sterile items, challenges with lidocaine ampules, patient claustrophobia from draping, and a lack of user preference for kit contents. Additional challenges included obscured ultrasound views, kinked guidewires, overall procedural untidiness, and considerable waste management issues.</p><p><strong>Conclusions: </strong>An intuitive kit that aligns with predictable human behavior and eliminates unnecessary multistep detours can reduce novice failure rates, cognitive load, and practice inconsistency, and it could also curb nonrecyclable waste from "backup" kits opened for a single missing item. By reframing CVC systems as sociotechnical solutions rather than static assortments of parts, the same design moves that minimize improvisation and coordination errors for physicians may also reduce dwell time and manipulation events for patients, thereby advancing the core triad of safety, procedural efficacy, and everyday usability. By examining how clinicians place central lines, this study reveals modifiable design flaws that perpetuate risk despite decades of procedural standardization. Contextual inquiry provides the evidentiary bridge between clinical imperatives to reduce complications and the practical realities of device use. Embedding such investigations at the outset of design and iteratively throughout product life c
背景:中心静脉导管(CVC)在当代重症监护、围手术期管理和紧急复苏中不可或缺,但其插入仍然充满了可预防的危害和低效率。目的:本文旨在通过使用以人为本的设计/定性研究方法,确定可以通过设备设计改进CVC放置的所有领域。方法:本定性研究是对CVC安置的语境调查,其中包括观察以及与医生的简短面对面访谈。它的目的是提供一个深度的理解,用证据来证明因果关系。本研究在三家医院进行:急诊科(ED)、重症监护病房(ICU)和手术室(OR)。在可能的情况下,在获得额外同意的情况下,以视频或静止摄影的方式记录会议,有时两者兼而有之。该研究包括19项观察和24次访谈。结果:在本研究中,CVC的插入方法在医院和护理环境中是一致的,在特定的护理环境中,例如缝线和敷料的使用或缺乏缝线和敷料的使用(例如,在特定的护理环境中缝线和敷料的使用/缺乏使用),在几个部分中具有中等的可变性。所描述和观察到的困难为设备设计留下了改进的空间。本研究结果表明,放置CVC系有34个离散步骤,大部分时间花在无菌制备过程中。由于设备/套件的设计,发现了一些挑战。这些包括缺少试剂盒中的基本材料,难以区分非无菌和无菌物品,利多卡因注射剂的挑战,悬垂引起的患者幽闭恐惧症,以及用户对试剂盒内容缺乏偏好。额外的挑战包括超声图像模糊、导丝缠绕、整体程序不整洁以及相当大的废物管理问题。结论:一个直观的工具包与可预测的人类行为保持一致,消除了不必要的多步骤弯路,可以降低新手的故障率、认知负荷和练习不一致,还可以减少因单个缺失项目而打开的“备用”工具包的不可回收浪费。通过将CVC系统重新构建为社会技术解决方案,而不是静态的部件分类,相同的设计动作可以最大限度地减少提供者的即兴和协调错误,也可以压缩患者的停留时间和操作事件,从而提高安全性,程序有效性和日常可用性的核心三合一。通过检查临床医生如何放置中心线,本研究揭示了可修改的设计缺陷,尽管数十年的程序标准化,但这些缺陷仍使风险持续存在。上下文调查提供了减少并发症的临床要求和设备使用的实际现实之间的证据桥梁。在设计之初就进行此类调查,并在整个产品生命周期中进行迭代,为患者和提供者提供了一条更安全、更高效、更人性化的中心静脉通路。临床试验:
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引用次数: 0
Expert Views on Criteria for Evaluation of Human Factors Methods: Qualitative Interview Study. 人因评价标准的专家意见方法:定性访谈研究。
IF 3 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-02-03 DOI: 10.2196/73324
Selvana Awad, Rachel Begg, Thomas Loveday, Andrew Baillie, Melissa Baysari

Background: Human factors (HF), or ergonomics, which explores the interaction between humans and systems, has been used to support design in safety-critical industries such as aviation, transportation, nuclear power, and manufacturing. HF methods have the potential to support the safe design of health IT; however, the evaluation of HF methods to determine their effectiveness and feasibility in this context has been limited.

Objective: The aim of this study was to identify criteria for evaluating HF methods when applied to real-world projects and to use these to propose a framework for method evaluation.

Methods: The study design was qualitative and descriptive and involved semistructured interviews with HF experts working across health and nonhealth industries in academic and/or practitioner roles. HF experts held a relevant degree (eg, ergonomics and HF engineering) and were actively using their HF expertise. Results were thematically analyzed.

Results: A total of 21 participants took part, and interviews lasted, on average, 52 (range 39-103) minutes. Participants mentioned that they did not routinely evaluate methods; however, when asked how they would evaluate methods, they outlined a range of criteria to support method evaluation. Overall, 5 criteria and 28 subcriteria were identified. High-level criteria included effectiveness, efficiency, ease of use and acceptability, and impact on the solution.

Conclusions: Results from this study were used to propose a framework for evaluating HF methods used in real-world health IT projects. The framework should provide organizations with valuable information on how to optimize the application and outcomes of HF methods and build HF capability within organizations, particularly where this capability may be lacking.

背景:人为因素(HF),或人体工程学,探索人与系统之间的相互作用,已被用于支持安全关键行业的设计,如航空,运输,核电和制造业。高频方法具有支持健康信息技术安全设计的潜力;然而,评估高频方法以确定其在这种情况下的有效性和可行性是有限的。目的:本研究的目的是确定在应用于实际项目时评估高频方法的标准,并使用这些标准来提出方法评估的框架。方法:研究设计采用定性和描述性的方法,并采用半结构化的访谈方式,对在卫生和非卫生行业担任学术和/或从业者角色的HF专家进行访谈。高频专家拥有相关学位(如人体工程学和高频工程学),并积极利用他们的高频专业知识。对结果进行主题分析。结果:共有21名参与者参与,访谈时间平均为52分钟(39-103分钟)。参与者提到他们没有定期评估方法;然而,当被问及他们将如何评价方法时,他们概述了一系列支持方法评价的标准。总的来说,确定了5个标准和28个子标准。高级标准包括有效性、效率、易用性和可接受性,以及对解决方案的影响。结论:本研究的结果被用来提出一个评估现实世界卫生IT项目中使用的心力衰竭方法的框架。该框架应该为组织提供关于如何优化高频方法的应用和结果以及在组织内建立高频能力的有价值的信息,特别是在这种能力可能缺乏的地方。
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引用次数: 0
Navigation, Adoption, and Use of Digital Health Technologies for Irritable Bowel Syndrome Self-Management: Focus Group Study of Patient Experience and Decision-Making. 肠易激综合征自我管理中数字健康技术的导航、采用和使用:患者体验和决策的焦点小组研究
IF 3 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-02-02 DOI: 10.2196/75012
Adrijana D'Silva, Nicolle Hua, Mary V Modayil, Judy Seidel, Deborah A Marshall

Background: Irritable bowel syndrome (IBS) is a common chronic gastrointestinal disorder that impairs bowel functions and patients' overall quality of life. IBS-focused digital health technologies (DHTs), including online health resources and mobile health (mHealth) apps, have recently proliferated for patient use. However, research exploring patients' experiences with navigating, adopting, or using commercial or publicly available DHTs for IBS self-management is limited.

Objective: This study aims to explore the user experiences and decision-making of patients with IBS as they navigate, adopt, and use diverse DHTs for disease self-management.

Methods: We conducted virtual semistructured focus group interviews to explore the experiences of patients with IBS using DHTs, including their perspectives on design and features, their decision-making process in using DHTs, and recommendations for improving user experience and uptake, given the heterogeneous nature of these tools. Canada-based patients with IBS who were using or had used mHealth apps to manage symptoms were recruited through purposive sampling from previous IBS-related studies. Discussions were transcribed verbatim, and inductive thematic analysis was performed using NVivo (version 14; Lumivero). A modified version of the Expanded Unified Theory of Acceptance and Use of Technology (UTAUT2) model was applied to guide the interpretation of the dynamic relationship between the influences on participants' decisions regarding DHT use.

Results: Among the 8 participants (all female; mean age 55.3, SD 13.5 years), two themes were identified: (1) uncertainty impacts the trustworthiness of DHTs, and (2) influences that drive the decision-making process to adopt and use DHTs. The observed influences aligned with the constructs of the UTAUT2 model (performance expectancy, effort expectancy, social influence, facilitating conditions, hedonic motivation, price value, and habit), with the addition of trust and risk in participants' decision-making. Digital health literacy and patient engagement were also raised as crucial components of participants' experiences and perspectives on DHTs.

Conclusions: Findings of this study highlight the current landscape of digital health in IBS and existing gaps and challenges for patients in navigating, adopting, and using DHTs for IBS self-management. While DHTs were generally viewed positively for their value and potential, patients with IBS consider several coexisting factors and trade-offs in their decision-making. Further investigations on the influences on and perspectives toward DHTs could enhance future development and iterations of these tools and improve patient confidence and uptake.

背景:肠易激综合征(IBS)是一种常见的慢性胃肠道疾病,会损害肠道功能和患者的整体生活质量。最近,以肠易激综合征为重点的数字医疗技术(dht),包括在线医疗资源和移动医疗(mHealth)应用程序,为患者提供了大量使用。然而,探索患者导航、采用或使用商业或公共可获得的dht进行IBS自我管理的经验的研究是有限的。目的:本研究旨在探讨肠易激综合征患者在导航、采用和使用多种dht进行疾病自我管理时的用户体验和决策。方法:我们进行了虚拟半结构化焦点小组访谈,以探讨IBS患者使用dht的经验,包括他们对设计和功能的看法,他们使用dht的决策过程,以及考虑到这些工具的异质性,对改善用户体验和吸收的建议。加拿大的肠易激综合征患者正在使用或曾经使用移动健康应用程序来管理症状,通过先前的肠易激综合征相关研究的有目的抽样招募。讨论被逐字转录,并使用NVivo(版本14;Lumivero)进行归纳主题分析。采用改进版的技术接受和使用扩展统一理论(UTAUT2)模型来指导解释影响参与者使用DHT决策的因素之间的动态关系。结果:在8名参与者(均为女性,平均年龄55.3岁,SD 13.5岁)中,确定了两个主题:(1)不确定性影响dht的可信度;(2)驱动dht采用和使用决策过程的影响。观察到的影响与UTAUT2模型的结构(绩效期望、努力期望、社会影响、促进条件、享乐动机、价格价值和习惯)一致,并在参与者的决策中增加了信任和风险。与会者还提出,数字卫生知识普及和患者参与是与会者关于dht的经验和观点的重要组成部分。结论:本研究的结果突出了IBS中数字健康的现状,以及患者在导航、采用和使用dht进行IBS自我管理方面存在的差距和挑战。虽然dht的价值和潜力通常被认为是积极的,但肠易激综合征患者在决策时考虑了几个共存的因素和权衡。进一步研究对dht的影响和前景,可以加强这些工具的未来开发和迭代,提高患者的信心和接受度。
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引用次数: 0
Exploring Medical Information Needs and Accessibility in Swedish Dental Care by Analysis of Documentation Workflows and Electronic Dental Records in Dalarna: Sociotechnical Qualitative Study. 通过分析瑞典达拉那的文档工作流程和电子牙科记录,探索瑞典牙科保健的医疗信息需求和可及性:社会技术定性研究。
IF 3 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-01-29 DOI: 10.2196/82691
Sahid Hasan Rahim, Nadia Davoody, Stefano Bonacina

Background: Despite growing evidence demonstrating the connection between oral and systemic health, medical and dental care remain institutionally divided. A significant consequence of this division is the lack of information sharing, which is particularly problematic in dental care, where knowing patients' medical information is crucial for providing safe and effective treatments. This separation poses additional challenges in Swedish regions with limited resources, such as Dalarna, where dental care practices would benefit from improved access to relevant medical information in their electronic dental record (EDR) systems.

Objective: This study aimed to explore how current documentation workflows and EDR systems support the medical information needs within dental care practices in Dalarna and consider what influence direct access to medical information could have.

Methods: The study adopted an exploratory-descriptive qualitative approach. Semi-structured interviews were conducted with dental practitioners working in general dental practices. Data collection followed a sociotechnical framework, and thematic analysis was performed to identify key medical information needs, as well as current workflow and system limitations. Conceptual models were developed to reflect these findings.

Results: Eighteen dental practitioners were interviewed. The identified medical information needs included specific types of medical conditions, pharmacological information, treatment history, and laboratory values. Furthermore, dental practitioners highlighted substantial challenges in existing documentation workflows and the EDR system. Proposed conceptual models demonstrated how integrating EDR systems with the Swedish National Patient Overview ("Nationell Patientöversikt") via National Service Platform ("Nationell Tjänsteplattform") could streamline workflows and enhance information accessibility.

Conclusions: The findings show a clear need to improve medical information accessibility in dental care. A solution is to facilitate interoperability and align digital infrastructure with the identified needs. The proposed recommendations offer a feasible starting point for improving medical information access in Swedish dental care, particularly in resource-constrained regions like Dalarna.

背景:尽管越来越多的证据表明口腔和全身健康之间存在联系,但医学和牙科保健在制度上仍然是分开的。这种划分的一个重要后果是缺乏信息共享,这在牙科保健中尤其严重,因为了解患者的医疗信息对于提供安全有效的治疗至关重要。这种分离给资源有限的瑞典地区带来了额外的挑战,例如Dalarna,这些地区的牙科保健实践将受益于通过电子牙科记录(EDR)系统改善对相关医疗信息的访问。目的:本研究旨在探讨当前的文档工作流程和EDR系统如何支持达拉那市牙科保健实践中的医疗信息需求,并考虑直接访问医疗信息可能产生的影响。方法:采用探索性-描述性定性研究方法。对在普通牙科诊所工作的牙科医生进行了半结构化访谈。数据收集遵循社会技术框架,并进行了专题分析,以确定关键的医疗信息需求以及当前的工作流程和系统限制。概念模型的发展反映了这些发现。结果:对18名牙科执业医师进行了访谈。确定的医疗信息需求包括特定类型的医疗条件、药理学信息、治疗历史和实验室值。此外,牙科从业者强调了现有文档工作流程和电子病历系统的重大挑战。提出的概念模型展示了如何通过国家服务平台(“Nationell Tjänsteplattform”)将EDR系统与瑞典国家患者概述(“Nationell Patientöversikt”)集成,从而简化工作流程并增强信息可及性。结论:研究结果表明,需要提高医疗信息的可及性。解决方案是促进互操作性,并使数字基础设施与确定的需求保持一致。拟议的建议为改善瑞典牙科保健的医疗信息获取提供了一个可行的起点,特别是在达拉尔纳等资源有限的地区。
{"title":"Exploring Medical Information Needs and Accessibility in Swedish Dental Care by Analysis of Documentation Workflows and Electronic Dental Records in Dalarna: Sociotechnical Qualitative Study.","authors":"Sahid Hasan Rahim, Nadia Davoody, Stefano Bonacina","doi":"10.2196/82691","DOIUrl":"10.2196/82691","url":null,"abstract":"<p><strong>Background: </strong>Despite growing evidence demonstrating the connection between oral and systemic health, medical and dental care remain institutionally divided. A significant consequence of this division is the lack of information sharing, which is particularly problematic in dental care, where knowing patients' medical information is crucial for providing safe and effective treatments. This separation poses additional challenges in Swedish regions with limited resources, such as Dalarna, where dental care practices would benefit from improved access to relevant medical information in their electronic dental record (EDR) systems.</p><p><strong>Objective: </strong>This study aimed to explore how current documentation workflows and EDR systems support the medical information needs within dental care practices in Dalarna and consider what influence direct access to medical information could have.</p><p><strong>Methods: </strong>The study adopted an exploratory-descriptive qualitative approach. Semi-structured interviews were conducted with dental practitioners working in general dental practices. Data collection followed a sociotechnical framework, and thematic analysis was performed to identify key medical information needs, as well as current workflow and system limitations. Conceptual models were developed to reflect these findings.</p><p><strong>Results: </strong>Eighteen dental practitioners were interviewed. The identified medical information needs included specific types of medical conditions, pharmacological information, treatment history, and laboratory values. Furthermore, dental practitioners highlighted substantial challenges in existing documentation workflows and the EDR system. Proposed conceptual models demonstrated how integrating EDR systems with the Swedish National Patient Overview (\"Nationell Patientöversikt\") via National Service Platform (\"Nationell Tjänsteplattform\") could streamline workflows and enhance information accessibility.</p><p><strong>Conclusions: </strong>The findings show a clear need to improve medical information accessibility in dental care. A solution is to facilitate interoperability and align digital infrastructure with the identified needs. The proposed recommendations offer a feasible starting point for improving medical information access in Swedish dental care, particularly in resource-constrained regions like Dalarna.</p>","PeriodicalId":36351,"journal":{"name":"JMIR Human Factors","volume":"13 ","pages":"e82691"},"PeriodicalIF":3.0,"publicationDate":"2026-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12854659/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146087551","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Online Tiered Screening for Mental Health Problems Among Refugees in Sweden: Validation Study. 瑞典难民心理健康问题的在线分层筛查:验证研究。
IF 3 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-01-29 DOI: 10.2196/82763
Jennifer Meurling, Elisabet Rondung, Youstina Demetry, Anahita Geranmayeh, Anna Leiler, Gerhard Andersson, Anna Bjärtå

Background: Refugees and asylum-seekers commonly experience numerous adverse and traumatic events and are therefore at increased risk of mental health problems. Despite the high need for mental health interventions, services tend to be underused by refugees and asylum-seekers, and various barriers compromise access. Digital, efficient screening, adapted for these groups, could facilitate initial assessment and increase accessibility to mental health services. We developed an internet-based tiered screening procedure (i-TAP) aiming to identify clinically relevant symptoms of major depressive disorder (MDD), anxiety disorder, posttraumatic stress disorder, and insomnia disorder among individuals with a refugee background. The i-TAP is an adaptive procedure with 3 tiers aiming to identify general mental distress in Tier 1, differentiate between symptoms in Tier 2, and assess the severity of symptoms in Tier 3. Each tier additionally functions as a gateway to further assessment, as a negative outcome terminates the procedure.

Objective: The purpose of this study was to evaluate the diagnostic test accuracy of the i-TAP, using structured clinical assessments as the reference standard.

Methods: In this prospective study, 70 adult participants with a refugee background, literate in Arabic, Dari, Farsi, or Swedish, and residing in Sweden, completed the i-TAP on tablets and participated in a subsequent structured diagnostic interview.

Results: It has been shown that the i-TAP could identify 91.7% (33/36) of individuals assessed with any psychiatric disorder, and correctly identified 82.1% of all positive cases of MDD, anxiety disorder, posttraumatic stress disorder, and insomnia disorder, with few false negative assessments. Overall test accuracy of the i-TAP ranged between 77.1% and 84.3%, depending on disorder. The tiered design could reduce item burden while maintaining accuracy. A vast majority of participants rated the user experience as positive. In this sample, 36/70 (51.4%) individuals were assessed with one or more psychiatric disorders and comorbidity was high.

Conclusions: The i-TAP may be a valid, efficient, and feasible screening tool for the identification of common psychiatric disorders among individuals with a refugee background in Sweden. The i-TAP could be implemented as a first screener in various settings, including online and in-person clinical practices. The digital, adaptive, multilingual format could facilitate early assessment and increase the availability of mental health services for refugees and asylum-seekers.

背景:难民和寻求庇护者通常经历许多不利和创伤事件,因此面临更大的精神健康问题风险。尽管对精神卫生干预措施的需求很高,但难民和寻求庇护者往往没有充分利用这些服务,各种障碍妨碍了获得这些服务。针对这些群体进行数字化、高效筛查,可促进初步评估并增加获得精神卫生服务的机会。我们开发了一种基于互联网的分层筛选程序(i-TAP),旨在识别具有难民背景的个体的重度抑郁症(MDD)、焦虑症、创伤后应激障碍和失眠症的临床相关症状。i-TAP是一种自适应程序,分为3个层次,旨在识别第1层的一般精神痛苦,区分第2层的症状,评估第3层症状的严重程度。每一层还作为进一步评估的门户,因为负面结果终止了该过程。目的:以结构化临床评估为参考标准,评价i-TAP诊断试验的准确性。方法:在这项前瞻性研究中,70名成年参与者具有难民背景,懂阿拉伯语、达里语、波斯语或瑞典语,居住在瑞典,在平板电脑上完成i-TAP,并参加随后的结构化诊断访谈。结果:i-TAP能识别出91.7%(33/36)的精神障碍患者,正确识别出82.1%的MDD、焦虑症、创伤后应激障碍和失眠症阳性病例,假阴性评估很少。i-TAP的总体测试准确度在77.1%到84.3%之间,具体取决于疾病。分层设计可以在保证准确性的同时减少项目负担。绝大多数参与者认为用户体验是积极的。在该样本中,70人中有36人(51.4%)被评估患有一种或多种精神疾病,合并症很高。结论:i-TAP可能是一种有效、高效和可行的筛查工具,用于识别瑞典难民背景的常见精神疾病。i-TAP可以在各种环境中作为第一筛选器,包括在线和面对面的临床实践。数字化、适应性、多语言格式可促进早期评估,并增加难民和寻求庇护者获得精神健康服务的机会。
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引用次数: 0
Demystifying Quality Metrics and Unveiling the True Measure of Quality of Care in Nursing Homes: Mixed Effects Analysis. 揭开质量指标的神秘面纱,揭示疗养院护理质量的真正衡量标准:混合效应分析。
IF 3 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-01-29 DOI: 10.2196/72770
Suhas Bharadwaj, Haneen Ali

Background: The 5-Star Quality Rating System for nursing homes plays a central role in evaluating quality of care, although it has both strengths and limitations. This system relies heavily on the Minimum Data Set and derives several quality measures (QMs) from it. In this study, we validated the effectiveness of the 5-Star Quality Rating System for nursing homes and its underlying QMs in estimating quality of care. We constructed a panel dataset of US nursing homes (n=15,416) active from May 2020 to June 2023, retrieving data from three major sources: (1) COVID-19 nursing home data, (2) Payroll-Based Journal data, and (3) nursing home QM snapshots. The outcome variables included (1) resident infection, (2) staff infection, or (3) resident and staff deaths. The predictor variables were the 5-Star Quality Rating System for nursing homes and its underlying QMs classified as structure, process, or outcome (SPO) QMs.

Objective: This study aims to evaluate the effectiveness of nursing home QMs by regressing nursing home COVID-19 outcomes on nursing home QMs, classified using the Donabedian SPO framework. We hypothesized that nursing homes with better structural quality (eg, greater staff availability, better skill mix, and so on), better process quality (eg, lower restraint use and higher vaccination rates), and better outcome quality (eg, lower number of residents with pressure ulcers and a lower number of resident falls) experienced better COVID-19 performance in terms of resident and staff infections and deaths.

Methods: To examine the association between the COVID-19 outcomes and SPO QMs, we imputed missing values in the dataset using random forest. Subsequently, we modeled the imputed dataset using hurdled zero-inflated negative binomial mixed effects models. The zero inflation model included factors influencing initial susceptibility to COVID-19 or factors influencing the possibility of death after COVID-19 had been contracted. The model estimates were conditioned on zero inflation and random effects.

Results: Staffing measures (P<.001 for all variables in all models), health deficiency scores (P<.001 for all variables in at least 1 model), COVID-19 hospitalization rates (P<.001 for all variables in at least 2 models), and vaccinations (P<.001 for all variables in at least 2 models) exhibited meaningful relationships with the COVID-19 outcomes, while the 5-star components, Medicaid dependency, and ownership showed no clear relationships.

Conclusions: Although widely used, the 5-Star Quality Rating System for nursing homes is an unreliable performance measure. Concerted efforts from lawmakers, policy makers, and lobbyists are needed to refine and enhance the measure, thereby ensuring its reliability and effectiveness.

背景:养老院的五星级质量评级系统在评估护理质量方面发挥着核心作用,尽管它既有优势也有局限性。该系统在很大程度上依赖于最小数据集,并从中派生出几个质量度量(QMs)。在这项研究中,我们验证了养老院的五星级质量评级系统及其潜在质量管理体系在估计护理质量方面的有效性。我们构建了2020年5月至2023年6月期间活跃的美国养老院(n=15,416)的面板数据集,从三个主要来源检索数据:(1)COVID-19养老院数据,(2)基于工资的期刊数据,(3)养老院QM快照。结果变量包括:(1)居民感染,(2)工作人员感染,或(3)居民和工作人员死亡。预测变量为养老院的五星级质量评级系统及其分类为结构、过程或结果(SPO)质量管理体系的潜在质量管理体系。目的:本研究旨在利用Donabedian SPO框架对养老院QMs的COVID-19结果进行回归,以评估养老院QMs的有效性。我们假设,结构质量较好的养老院(例如,更多的工作人员可用性,更好的技能组合等),更好的流程质量(例如,更低的约束使用和更高的疫苗接接率),以及更好的结果质量(例如,更少的居民患压疮和更少的居民跌倒)在居民和工作人员感染和死亡方面表现更好。方法:为了检验COVID-19结局与SPO QMs之间的关系,我们使用随机森林方法在数据集中输入缺失值。随后,我们使用跨栏零膨胀负二项混合效应模型对输入数据集进行建模。零膨胀模型包括影响COVID-19初始易感性或影响COVID-19感染后死亡可能性的因素。模型估计的条件是零通货膨胀和随机效应。结论:养老院的五星级质量评价体系虽然被广泛使用,但它是一种不可靠的绩效评价指标。为了确保其可靠性和有效性,需要国会议员、政策制定者和游说团体的共同努力。
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引用次数: 0
Parental Influence on Children's Media Use in South Korea: National Population-Based Study. 韩国父母对儿童媒体使用的影响:基于全国人口的研究。
IF 3 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-01-28 DOI: 10.2196/75292
Ji Young Kim, Ah Jung Yang, Hye Eun Lee

Background: To better understand the effects of media use on children, it is essential to examine the various factors influencing the media use of digital native children. In the situational context, parental media usage, parents' attitudes toward media, and parenting styles have all been identified as significant factors influencing children's media use. This study focuses on the key factors and examines these relationships in greater depth, drawing on existing research to understand their impact on the media usage patterns of digital native children.

Objective: This study examines parental influences related to young children's media use in Korea over a 3-year period (2022-2024) using independent, nationally representative cohorts.

Methods: Using multigroup structural equation modeling, we analyzed data from 3 independent parent-reported cohorts (for 2022, n=1058; for 2023, n=1020; for 2024, n=1020) to investigate how parental media habits, attitudes, and distinct parenting styles predict children's daytime and nighttime media consumption.

Results: The online survey results revealed that parental media time, particularly for mothers, consistently correlated with higher levels of children's daytime media use (β=.002-.003). Positive parental attitudes toward media increased children's daytime media use (β=.028-.102), whereas negative attitudes had a limited effect (β=-.069-.140). Among the 7 parenting styles, positive parenting consistently reduced children's daytime media use in 2022 and 2023 (β=-.228 for 2022, β=-.215 for 2023), but harsh punishment emerged as the strongest factor in daytime media use in 2024 (β=-.078 for 2022, β=-.090 for 2023, and β=-.072 for 2024). Notably, parenting styles showed no significant effect on children's nighttime media use throughout the study, suggesting that parental influence may be more effective during daytime hours.

Conclusions: This analysis extends existing research by differentiating media use patterns across time periods and highlights the evolving influence of parenting styles. These findings have implications for the development of targeted parental guidelines for managing young children's media exposure, especially as digital media continues to become a pervasive part of daily life.

背景:为了更好地了解媒体使用对儿童的影响,有必要研究影响数字原生儿童媒体使用的各种因素。在情境情境中,父母的媒体使用、父母对媒体的态度和父母的教养方式都被认为是影响儿童媒体使用的重要因素。本研究侧重于关键因素,并更深入地考察了这些关系,利用现有研究来了解它们对数字原住民儿童媒体使用模式的影响。目的:本研究通过独立的、具有全国代表性的队列,调查了韩国3年(2022-2024)期间父母对幼儿媒体使用的影响。方法:采用多组结构方程模型,对来自3个独立父母报告队列(2022年,n=1058; 2023年,n=1020; 2024年,n=1020)的数据进行分析,探讨父母的媒体习惯、态度和不同的父母方式如何影响儿童白天和夜间的媒体消费。结果:在线调查结果显示,父母的媒体时间,特别是母亲的媒体时间,始终与孩子白天使用媒体的水平相关(β= 0.002 - 0.003)。父母对媒体的积极态度增加了儿童白天对媒体的使用(β= 0.028 - 0.102),而消极态度的影响有限(β=- 0.069 - 0.140)。在7种教养方式中,积极的教养方式在2022年和2023年持续减少儿童日间媒体使用(2022年β=- 0.228, 2023年β=- 0.215),但严厉的惩罚在2024年成为影响儿童日间媒体使用的最强因素(2022年β=- 0.078, 2023年β=- 0.090, 2024年β=- 0.072)。值得注意的是,在整个研究过程中,父母的教养方式对孩子夜间使用媒体没有显著影响,这表明父母的影响在白天可能更有效。结论:该分析通过区分不同时期的媒体使用模式扩展了现有的研究,并强调了父母教养方式的不断变化的影响。这些发现对制定有针对性的家长指导方针以管理幼儿的媒体接触具有重要意义,特别是在数字媒体继续成为日常生活中普遍存在的一部分的情况下。
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JMIR Human Factors
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