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Experiences of Using Online Peer Forums Among People With Postpartum Psychosis: Interpretative Phenomenological Study. 产后精神病患者使用在线同伴论坛的经验:解释性现象学研究。
IF 3 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-12-24 DOI: 10.2196/80717
Katherine Williams, Fiona Lobban, Elizabeth Chamberlain

Background: Although research has found online peer support forums to be helpful for those with mental health conditions, no studies have explored the experiences of those who use forums for support with postpartum psychosis (PP) specifically.

Objective: This study aimed to understand the lived experiences of using online forums for PP, and how this form of support differs from professional and other informal support.

Methods: This study used a qualitative approach, including semistructured interviews with 8 participants. Recruitment took place via an online forum run by a charity called Action on Postpartum Psychosis. Transcripts were analyzed using interpretative phenomenological analysis.

Results: Four themes were developed in line with participants' experiences (1) from isolation to connection: validation, growth, and hope from shared experiences; (2) complementing not replacing: filling the gaps in support; (3) impacts of privacy, representation, and readiness to share on engagement; and (4) relational experiences within peer support: altruism, boundaries, and comparison. All participants believed forums were helpful to their well-being and recovery; however, some also reported difficulties with engagement, comparison, and regulating their own use. Findings suggest that forums may benefit from being designed in a way that protects users and their identities, for example, via trigger warnings and setting boundaries.

Conclusions: Peer online forums offer a unique and potentially effective addition to existing support provided by professionals and personal connections. Professionals should signpost people experiencing PP to forums, but should also understand the support that may be needed in terms of monitoring use and ensuring that appropriate boundaries are put into place.

背景:虽然研究发现在线同伴支持论坛对那些有心理健康状况的人有帮助,但没有研究专门探讨那些使用论坛支持产后精神病(PP)的人的经历。目的:本研究旨在了解使用在线论坛进行PP的生活体验,以及这种形式的支持与专业支持和其他非正式支持有何不同。方法:本研究采用定性研究方法,包括对8名参与者进行半结构化访谈。招聘是通过一个名为“产后精神病行动”的慈善机构运营的在线论坛进行的。使用解释性现象学分析分析转录本。结果:根据参与者的经历(1)从孤立到联系,开发了四个主题:来自共享经历的验证、成长和希望;(2)补而不补:补支座上的空隙;(3)隐私、代表性和分享意愿对参与的影响;(4)同伴支持中的关系体验:利他主义、边界和比较。所有与会者都认为论坛有助于他们的幸福和康复;然而,一些人也报告了在参与、比较和规范自己的使用方面的困难。研究结果表明,论坛可以通过保护用户及其身份的方式进行设计,例如通过触发警告和设置边界。结论:同行在线论坛提供了一个独特的和潜在有效的补充现有的专业人士和个人关系提供的支持。专业人员应该为经历PP的人指点论坛,但也应该了解在监控使用和确保适当的边界设置方面可能需要的支持。
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引用次数: 0
Optimizing SloMo, a Digitally Supported Therapy Targeting Paranoia, for Implementation: Inclusive, Human-Centered Design Study. 优化SloMo,一种针对偏执的数字支持疗法,用于实施:包容性,以人为本的设计研究。
IF 3 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-12-22 DOI: 10.2196/75377
Thomas Gant, Kathryn M Taylor, Thomas Ward, Philippa Garety, Amy Hardy
<p><strong>Background: </strong>Despite the promise of digital therapeutics in providing scalable interventions for psychosis, translating them from clinical trials to routine care is challenging. SloMo is an evidence-based, digitally supported cognitive behavioral therapy for psychosis comprising a web-based therapy platform and mobile app. The therapy encourages individuals to slow down for a moment, to address fast-thinking habits fueling paranoia. SloMo has received a NICE Early Value Assessment recommendation for use in the National Health Service to address evidence gaps related to its use in the real world, and an implementation study is underway.</p><p><strong>Objective: </strong>This study aimed to optimize the SloMo software for implementation by addressing limitations of the first release, reducing technology complexity, and improving user experience, to increase equitable outcomes.</p><p><strong>Methods: </strong>An inclusive, human-centered design methodology was used to optimize SloMo. The redesign sought to reduce the technology's complexity and improve the user experience for diverse patients and therapists. The Double Diamond framework structured the iterative redesign, integrating insights from patient and public involvement consultants, therapists, and a transdisciplinary co-design team. The Double Diamond process was facilitated through 24 transdisciplinary workshops. These were supported by the following methods: identifying implementation barriers through desk research of SloMo's evidence and qualitative interviews with experts by experience (n=2); redefining user needs; iteratively developing solutions through user testing sessions with service user consultants (n=32); and validating the minimum viable product through think-aloud testing sessions with therapist (n=10) and service user (n=11) consultants.</p><p><strong>Results: </strong>Users wanted a form of cognitive behavioral therapy for psychosis that was usable, trustworthy, enjoyable, personalized, normalizing, and memorable. The redesign, therefore, included a minimalist user interface, more diverse lived experience vignette content, enhanced agency over data, greater representation of protected characteristics and their intersectionality, and intuitive navigation. Feedback from a purposively sampled patient and therapist sample validated the redesign as it was associated with a strong user experience, particularly in relation to usability and usefulness.</p><p><strong>Conclusions: </strong>The study produced a redesign of the SloMo software optimized for real-world use, whilst retaining fidelity to the therapeutic content of the previous version. Through an inclusive, human-centered approach, the optimized design of SloMo addresses barriers to adoption by reducing complexity and fostering accessibility. This study underscores the value of integrating lived experience involvement into digital therapeutics to support scalable, equitable, and sustainable mental health
背景:尽管数字治疗有望为精神病提供可扩展的干预措施,但将其从临床试验转化为常规护理仍具有挑战性。SloMo是一种基于证据、数字支持的精神病认知行为疗法,包括一个基于网络的治疗平台和移动应用程序。该疗法鼓励患者暂时放慢速度,解决引发偏执的快速思维习惯。SloMo已收到NICE早期价值评估建议,用于国家卫生服务,以解决其在现实世界中使用的证据差距,并且正在进行实施研究。目的:本研究旨在通过解决首次发布的局限性、降低技术复杂性和改善用户体验来优化SloMo软件的实现,以增加公平的结果。方法:采用包容性、以人为本的设计方法对SloMo进行优化设计。重新设计旨在降低技术的复杂性,并改善不同患者和治疗师的用户体验。双钻石框架构建了反复的重新设计,整合了来自患者和公众参与顾问、治疗师和跨学科合作设计团队的见解。通过24个跨学科讲习班促进了双钻石进程。这些研究得到以下方法的支持:通过对SloMo证据的案头研究和经验专家的定性访谈来确定实施障碍(n=2);重新定义用户需求;通过与服务用户顾问进行用户测试,反复开发解决方案(n=32);并通过与治疗师(n=10)和服务用户(n=11)咨询师的有声思考测试会话来验证最小可行产品。结果:用户想要一种可用的、值得信赖的、愉快的、个性化的、正常化的、难忘的精神病认知行为疗法。因此,重新设计包括极简主义的用户界面,更多样化的生活体验内容,增强的数据代理,更多的受保护特征及其交叉性的代表,以及直观的导航。从有目的的患者和治疗师样本中获得的反馈验证了重新设计,因为它与强大的用户体验有关,特别是在可用性和有用性方面。结论:该研究对SloMo软件进行了重新设计,优化了现实世界的使用,同时保留了对以前版本治疗内容的保真度。通过包容性的、以人为本的方法,SloMo的优化设计通过降低复杂性和促进可访问性来解决采用障碍。这项研究强调了将生活体验融入数字治疗的价值,以支持可扩展、公平和可持续的精神卫生保健解决方案。
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引用次数: 0
Dynamic Indicators of Adherence and Retention in Adults Using a Digital Mental Health App: Longitudinal Observational Analysis From the Brighten Study. 使用数字心理健康应用程序的成人依从性和保留率的动态指标:来自照亮研究的纵向观察分析。
IF 3 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-12-22 DOI: 10.2196/69464
Dylan Hamitouche, Youcef Barkat, Deven Parekh, Eva Hammer, David Benrimoh

Background: Making optimal use of mobile health technologies requires the validation of digital biomarkers, which in turn demands high levels of participant adherence and retention. However, current remote digital health studies have high attrition rates and low participant adherence, which may introduce bias and limit the generalizability of their findings.

Objective: This study aimed to identify longitudinal indicators of participant retention and adherence, which may serve to develop strategies to improve data collection in digital health studies and improve understanding of how study cohorts are shaped by participant withdrawal and nonadherence.

Methods: We performed secondary analyses on the Brighten study, which consisted of 2 remote, smartphone-based randomized controlled trials evaluating mobile apps for depression treatment, enrolling 2193 participants in total. Participants were asked, after baseline assessment, to complete 7 digital questionnaires regularly. We assessed adherence to digital questionnaires, engagement (postbaseline participation), and retention rates (the proportion of participants who continued completing questionnaires over time) as outcomes. We investigated the relationship between these outcomes and both static measures (eg, demographics and average questionnaire scores) and dynamic measures (eg, changes in questionnaire scores over time).

Results: The study included 2201 participants, of whom 1093 completed at least 1 nonbaseline questionnaire, with a median completion rate of 37.6% (IQR 15.5%-67.9%). We found significantly higher adherence rates in participants who were less depressed on average over the course of the study (t752=-5.63; P<.001) and in those who perceived clinical improvement (t744=3.78; P=.001). There were significant demographic differences in adherence and engagement, including differences by gender, race, education, income, and income satisfaction. Participants who were more depressed at baseline were more likely to withdraw before completing any nonbaseline questionnaire (t1917=-2.53; P=.01). However, participants who showed improvement in depressive symptoms during the study showed better adherence (Mann-Whitney U=127,084; P<.001) and retention (hazard ratio 0.78, 95% CI 0.67-0.91; P=.002), despite showing greater depressive symptoms at baseline.

Conclusions: We show that participants' clinical trajectory of depressive symptoms, as well as their perception of improvement, are important indicators of engagement, adherence, and retention. Expanding knowledge regarding these longitudinal indicators may improve interpretation of outcomes and help build strategies to improve retention and adherence in future clinical trials.

背景:优化移动医疗技术的使用需要数字生物标志物的验证,这反过来又要求参与者的高水平依从性和保留率。然而,目前的远程数字健康研究具有高流失率和低参与者依从性,这可能会引入偏见并限制其研究结果的可推广性。目的:本研究旨在确定参与者保留和依从性的纵向指标,这可能有助于制定改进数字健康研究数据收集的策略,并提高对参与者退出和不依从性如何影响研究队列的理解。方法:我们对“照亮”研究进行了二次分析,该研究包括两项基于智能手机的远程随机对照试验,评估移动应用程序治疗抑郁症的效果,总共招募了2193名参与者。在基线评估之后,参与者被要求定期完成7份电子问卷。我们评估了数字问卷的依从性、参与度(基线后参与)和保留率(随着时间的推移继续完成问卷的参与者比例)作为结果。我们调查了这些结果与静态测量(如人口统计和平均问卷得分)和动态测量(如问卷得分随时间的变化)之间的关系。结果:研究纳入2201名参与者,其中1093人完成了至少1份非基线问卷,中位完成率为37.6% (IQR为15.5%-67.9%)。我们发现,在研究过程中,平均抑郁程度较低的参与者的依从率显著更高(t752=-5.63);结论:我们表明,参与者的抑郁症状的临床轨迹,以及他们对改善的感知,是参与、依从性和保留的重要指标。扩大对这些纵向指标的了解可能会改善对结果的解释,并有助于制定策略,以提高未来临床试验中的保留和依从性。
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引用次数: 0
Bridging Policy and Practice in Telemedicine Follow-Up Identification: Multicenter Mixed Methods Study in Beijing. 北京远程医疗随访识别的衔接政策与实践:多中心混合方法研究。
IF 3 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-12-19 DOI: 10.2196/75964
Yanli Lyu, Xi Li, Huixian Li, Mingyu Gu, Xuedong Xu, Yipei Wang, Changxiao Jin
<p><strong>Background: </strong>Telemedicine services have been developing rapidly worldwide. Following the 2018 policy enabling telemedicine for follow-up patients, this service model has gradually gained popularity in China. However, little has been done to understand the policy's implementation across different types of medical institutions or to evaluate its effectiveness.</p><p><strong>Objective: </strong>This study aims to (1) investigate the patient eligibility assessment process in various types of institutions for telemedicine services in Beijing, (2) elucidate institutions' rationale for adopting such approaches, (3) analyze discrepancies between policy and practice, and (4) provide references for the development of telemedicine services.</p><p><strong>Methods: </strong>This mixed methods study involved 36 medical institutions in Beijing, determined based on placing in the top 20% for both service volume and service quality in 2023. The study was conducted in 2 phases. First, quantitative analyses were conducted based on the questionnaires collected from each institution's contact to gather information about the assessment process and patient prerequisites. Subsequently, qualitative analyses were conducted through thematic analysis of 36 semistructured interviews with each institution's contact to acquire their considerations of this practice.</p><p><strong>Results: </strong>These 36 institutions contributed 968,786 telemedicine visits, representing 89.5% of the total service volume in Beijing. In practice, each of the visits underwent a 2-stage eligibility assessment before the physician officially accepted the patient's request. In the first stage, for assessment approaches, 86.2% (25/29) of the nonprofit, tertiary hospitals and 14.3% (1/7) of the private, for-profit institutions automatically assessed patient eligibility, while others did it manually. The assessment was based on the scope of previous visit location, diagnosis of previous visits, and visit interval. For the scope of visit location, 22 hospitals required prior visits to the same institution. For diagnosis, 7 hospitals required patients to have an identical diagnosis. For visit intervals, 11 hospitals required it to be within 6 months. The second stage assessment was conducted by physicians. Compared with policy requirements, nonprofit hospitals had stricter requirements for the scope of visit locations. The main reasons for these discrepancies included distrust in the medical outcomes from other institutions (19/26, 73.1%) and difficulties in handling interinstitutional medical disputes (18/26, 69.2%). In addition, 61.1% (22/36) of the institutions indicated that terminations of telemedicine services were primarily due to the patient's conditions.</p><p><strong>Conclusions: </strong>This pioneering multicenter, mixed methods study delineated the patient eligibility assessment process for telemedicine services in Beijing. Discrepancies were identified between real-world
背景:远程医疗服务在世界范围内发展迅速。随着2018年政策允许远程医疗随访患者,这种服务模式在中国逐渐普及。然而,了解该政策在不同类型医疗机构中的执行情况或评估其有效性的工作却很少。目的:本研究旨在(1)了解北京市各类机构对远程医疗服务的患者资格评估过程,(2)阐明机构采用这种方法的理由,(3)分析政策与实践的差异,(4)为远程医疗服务的发展提供参考。方法:采用混合方法研究北京市36家医疗机构,以2023年服务量和服务质量均进入前20%的医疗机构为研究对象。本研究分两个阶段进行。首先,通过从各机构联系人处收集的问卷进行定量分析,收集评估过程和患者先决条件的信息。随后,通过对与每个机构的联系人进行的36次半结构化访谈的专题分析进行定性分析,以获得他们对这种做法的考虑。结果:36家机构的远程医疗访问量为968,786次,占北京市总服务量的89.5%。在实践中,在医生正式接受患者的请求之前,每次就诊都要进行2阶段的资格评估。在第一阶段,对于评估方法,86.2%(25/29)的非营利性三级医院和14.3%(1/7)的私营营利性机构自动评估患者资格,而其他机构则手动评估。评估基于既往就诊地点、既往就诊诊断和就诊间隔的范围。就访问地点范围而言,22家医院要求事先访问同一家机构。在诊断方面,7家医院要求患者有相同的诊断。对于就诊间隔,11家医院要求在6个月内。第二阶段的评估由医生进行。与政策要求相比,非营利性医院对就诊地点范围的要求更为严格。造成这些差异的主要原因是不信任其他机构的医疗结果(19/26,73.1%)和处理机构间医疗纠纷困难(18/26,69.2%)。此外,61.1%(22/36)的机构表示,终止远程医疗服务主要是由于患者的病情。结论:这项开创性的多中心、混合方法研究描述了北京远程医疗服务的患者资格评估过程。确定了现实世界实践与监管先决条件之间的差异。造成这些差异的关键因素包括政策的模糊性和不同机构类型的优先事项不同。我们的研究结果建议提高政策清晰度,放宽对新患者的监管,加强对远程医疗服务的监管,以提高远程医疗的质量和可及性。
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引用次数: 0
Investigating How Clinicians Form Trust in an AI-Based Mental Health Model: Qualitative Case Study. 调查临床医生如何在基于人工智能的心理健康模型中形成信任:定性案例研究。
IF 3 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-12-19 DOI: 10.2196/79658
Anthony Kelly, Niharika Bhardwaj, Trine Theresa Holmberg Sainte-Marie, Pepijn Van de Ven, Ruth Melia, John Eustis Williams, Kim Mathiasen, Amalie Søgaard Nielsen

Background: Trust in artificial intelligence (AI) remains a critical barrier to the adoption of AI in mental health care. This study explores the formation of trust in an AI mental health model and its human-computer interface among clinicians at a web-based mental health clinic in the Region of Southern Denmark with national coverage.

Objective: This study aims to explore clinicians' perspectives on how trust is built in the context of an AI-supported mental health screening model and to identify the factors that influence this process.

Methods: This was a qualitative case study using semistructured interviews with clinicians involved in the pilot of a mental health AI model. Thematic analysis was used to identify key factors contributing to trust formation.

Results: Clinicians' initial attitudes toward AI were shaped by prior positive experiences with AI and their perception of AI's potential to reduce cognitive load in routine screening. Trust development followed a sequential pattern resembling a "trust journey": (1) sense-making, (2) risk appraisal, and (3) conditional decision to rely. Trust formation was supported by the explainability of the model, particularly through (1) visualization of confidence and uncertainty through violin plots, aligning with the clinicians' expectations of decision ambiguity; (2) feature attribution for and against predictions, which mirrored clinical reasoning; and (3) use of pseudo-sumscores in the AI model, which increased interpretability by presenting explanations in familiar clinical formats. Trust was contextually bounded to low-risk clinical scenarios, such as preinterview patient screening, and contingent on safety protocols (eg, suicide risk flagging). The use of both structured and unstructured patient data was seen as key to expanding trust into more complex clinical contexts. Participants also expressed a need for ongoing evaluation data to reinforce and maintain trust.

Conclusions: Clinicians' trust in AI tools is contextually and sequentially constructed, influenced by both model performance and alignment with clinical reasoning. Interpretability features were essential in establishing intrinsic trust, particularly when presented in ways that resonate with clinical norms. For broader acceptance and responsible deployment, trust must be supported by rigorous evaluation data and the inclusion of clinically relevant data types in model design.

背景:对人工智能(AI)的信任仍然是人工智能在精神卫生保健中应用的关键障碍。本研究探讨了在丹麦南部地区一个覆盖全国的基于网络的心理健康诊所,临床医生对人工智能心理健康模型及其人机界面的信任形成。目的:本研究旨在探讨临床医生在人工智能支持的心理健康筛查模型背景下如何建立信任的观点,并确定影响这一过程的因素。方法:这是一项定性案例研究,使用半结构化访谈与参与心理健康人工智能模型试点的临床医生进行访谈。专题分析用于确定促进信任形成的关键因素。结果:临床医生对人工智能的最初态度是由先前使用人工智能的积极经历和他们对人工智能在常规筛查中减少认知负荷的潜力的看法所决定的。信任发展遵循类似于“信任之旅”的顺序模式:(1)意义制定,(2)风险评估,(3)有条件的依赖决策。模型的可解释性支持了信任的形成,特别是通过(1)小提琴情节对信心和不确定性的可视化,与临床医生对决策模糊性的期望一致;(2)支持和反对预测的特征归因,反映了临床推理;(3)在人工智能模型中使用伪积分,通过以熟悉的临床格式呈现解释来提高可解释性。信任在情境上局限于低风险的临床场景,如访谈前的患者筛查,并取决于安全协议(如自杀风险标记)。结构化和非结构化患者数据的使用被视为将信任扩展到更复杂的临床环境的关键。与会者还表示需要持续的评估数据,以加强和维持信任。结论:临床医生对人工智能工具的信任是根据情境和顺序构建的,受模型性能和与临床推理的一致性的影响。可解释性特征对于建立内在信任至关重要,特别是当以与临床规范产生共鸣的方式呈现时。为了更广泛的接受和负责任的部署,信任必须得到严格的评估数据和在模型设计中纳入临床相关数据类型的支持。
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引用次数: 0
Organizational Readiness for Change in the Era of Smart Hospital Wards: Qualitative Study of Health Care Workers' Insights. 智能医院病房时代的组织变革准备:卫生保健工作者见解的定性研究。
IF 3 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-12-18 DOI: 10.2196/81932
Hui Wen Lim, Jennifer Sumner, Abigail Ang, Camille Keck, Emily Hwee Hoon Chew, Alexander Wenjun Yip

Background: Technology is rapidly reshaping conventional hospital environments into smart spaces, enhancing care, improving clinical workflows, and reducing workloads. However, successful implementation depends not only on the effectiveness of the technology but also on organizational readiness for change.

Objective: This study aimed to identify the key enablers and barriers to readiness for change for a smart hospital ward initiative.

Methods: We conducted a qualitative study to gauge organizational readiness for change for a smart ward initiative. Using purposive sampling, we captured diverse views from clinicians, IT staff, operational support staff, and health care redesign staff. Data were coded deductively under 3 key domains in Weiner's theory of organizational readiness: change efficacy, change commitment, and contextual factors. Subthemes were derived inductively under each domain.

Results: We interviewed 19 participants, including clinicians and support staff. Six subthemes emerged: (1) perceived valence and feasibility; (2) transparency and trust in management; (3) shared understanding and readiness to act; (4) resources, training, and staff capability; (5) innovation culture; and (6) past experiences. Participants viewed the initiative as valuable and were motivated to change, citing that the institution's innovation culture was a key enabler. However, there were key barriers, including unclear timelines, inconsistent training, limited resources, and a lack of infrastructure to support innovation. Concerns about overreliance on technology were also prominent, with staff wary of its impact on clinical judgment and system reliability.

Conclusions: Enabling readiness for the smart ward initiative requires transparent communication of timelines and project awareness, particularly for ground staff, the development of training frameworks, and adequate prioritization of innovation. Alleviating commonly reported technology concerns, such as overreliance, loss of human touch, and system reliability, will also be key to adoption and sustainability.

背景:技术正在迅速将传统医院环境重塑为智能空间,加强护理,改善临床工作流程,并减少工作量。然而,成功的实施不仅取决于技术的有效性,还取决于组织对变化的准备程度。目的:本研究旨在确定智能医院病房变革准备就绪的关键促成因素和障碍。方法:我们进行了一项定性研究,以衡量组织对智能病房计划变化的准备程度。通过有目的的抽样,我们收集了来自临床医生、IT人员、运营支持人员和医疗保健重新设计人员的不同观点。数据在Weiner组织准备理论的三个关键领域:变革效能、变革承诺和情境因素下进行演绎编码。在每个域下归纳派生出子主题。结果:我们采访了19名参与者,包括临床医生和支持人员。出现了六个子主题:(1)感知效价和可行性;(2)透明度和对管理层的信任;(3)共同的理解和行动意愿;(四)资源、培训和人员能力;(5)创新文化;(6)过往经历。与会者认为这一举措很有价值,并有动力做出改变,指出该机构的创新文化是一个关键的推动因素。然而,存在一些关键的障碍,包括时间表不明确、培训不一致、资源有限以及缺乏支持创新的基础设施。对过度依赖技术的担忧也很突出,工作人员担心其对临床判断和系统可靠性的影响。结论:为智能病房计划做好准备,需要对时间表和项目意识进行透明的沟通,特别是对地勤人员,培训框架的制定,以及充分的创新优先级。减轻通常报道的技术问题,如过度依赖、失去人的接触和系统可靠性,也将是采用和可持续性的关键。
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引用次数: 0
Perceptions of User-Generated Content as a Source of Health Messages in Smoking Cessation Mobile Interventions: Focus Group Study. 用户生成内容作为戒烟移动干预中健康信息来源的认知:焦点小组研究。
IF 3 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-12-17 DOI: 10.2196/76804
Michael Wakeman, Lydia Tesfaye, Tim Gregory, Erin Leahy, Gunnar Baskin, Greg Gruse, Brandon Kendrick, Sherine El-Toukhy

Background: Health messages are integral to smoking cessation interventions. Common approaches to health message development include expert-crafted messages and audience-generated messages, which produce messages that can be monotonic, didactic, and limited in number. We introduce an alternative approach to health message development that relies on user-generated content available on open-content platforms as a source of health messages.

Objective: We examined the acceptability of user-generated content curated from Twitter (subsequently rebranded X) as a source of health support messages in a newly developed smoking cessation mobile intervention called Quit Journey and the optimal timing and frequency with which health messages can be deployed to support app users in real time.

Methods: A total of 12 semistructured focus groups were held with 38 young adults with low socioeconomic status who smoked cigarettes, wanted to quit, and were aged 18 to 29 years. Focus groups were held virtually on GoTo Meeting, audio recorded, and transcribed verbatim. Deductive thematic analysis was used, with themes based on 5 constructs from the second unified theory of acceptance and use of technology (ie, effort expectancy, facilitating conditions, hedonic motivation, performance expectancy, and social influence) and negative, neutral, and positive sentiment.

Results: Participants perceived user-generated content positively (56/108, 51.9% of the quotes) and focused on their perceived usefulness (37/108, 34.3% of the quotes). User-generated content was perceived as authentic, nonrepetitive support from people with similar real-life experiences. Negative or sarcastic user-generated content elicited negative reactions from participants. Participants preferred receiving 3 or fewer daily messages, ideally before cravings. Suggestions focused on the need to screen user-generated content before its inclusion in the app library and allow app users to customize message frequency and timing.

Conclusions: User-generated content was deemed an acceptable source of health messages. This content can improve the efficacy and effectiveness of smoking cessation interventions by increasing their pool of unique messages that may be better received and more persuasive than expert-curated content. User-generated content can be used to curate health messages for all medical conditions and behaviors with relevant publicly available online content for integration in behavioral interventions given its high volume, brevity, and narrative-like nature. Future research is needed to investigate the effects of user-generated content on health behaviors and identify the theoretical mechanisms for these effects.

背景:健康信息是戒烟干预措施的组成部分。健康信息开发的常见方法包括专家编写的信息和受众生成的信息,后者产生的信息可能单调、说教,而且数量有限。我们介绍了一种健康信息开发的替代方法,该方法依赖于开放内容平台上可用的用户生成内容作为健康信息的来源。目的:我们研究了在新开发的戒烟移动干预中,Twitter(随后更名为X)作为健康支持信息来源的用户生成内容的可接受性,以及健康信息可以部署到实时支持应用程序用户的最佳时间和频率。方法:对38名年龄在18 ~ 29岁、社会经济地位低、吸烟、想戒烟的年轻人进行了12个半结构化的焦点小组研究。焦点小组在GoTo会议上举行,录音,并逐字抄录。采用演绎主题分析,主题基于第二种技术接受和使用统一理论中的5个构念(即努力期望、便利条件、享乐动机、绩效期望和社会影响)以及消极、中性和积极情绪。结果:参与者对用户生成内容的看法是积极的(56/108,51.9%的引用),并关注其感知的有用性(37/108,34.3%的引用)。用户生成的内容被认为是来自有相似现实经历的人的真实的、不重复的支持。负面或讽刺的用户生成的内容引起了参与者的负面反应。参与者更喜欢每天收到3条或更少的信息,最好是在渴望之前。建议的重点是,在将用户生成的内容纳入应用程序库之前,需要对其进行筛选,并允许应用程序用户自定义消息频率和时间。结论:用户生成的内容被认为是可接受的健康信息来源。这些内容可以提高戒烟干预措施的功效和效果,因为它们增加了独特的信息,这些信息可能比专家策划的内容更容易被接受,更有说服力。用户生成的内容可用于为所有医疗状况和行为策划健康信息,并提供相关的公开在线内容,以便将其整合到行为干预中,因为这些内容容量大、篇幅短、具有叙事性。未来的研究需要调查用户生成内容对健康行为的影响,并确定这些影响的理论机制。
{"title":"Perceptions of User-Generated Content as a Source of Health Messages in Smoking Cessation Mobile Interventions: Focus Group Study.","authors":"Michael Wakeman, Lydia Tesfaye, Tim Gregory, Erin Leahy, Gunnar Baskin, Greg Gruse, Brandon Kendrick, Sherine El-Toukhy","doi":"10.2196/76804","DOIUrl":"10.2196/76804","url":null,"abstract":"<p><strong>Background: </strong>Health messages are integral to smoking cessation interventions. Common approaches to health message development include expert-crafted messages and audience-generated messages, which produce messages that can be monotonic, didactic, and limited in number. We introduce an alternative approach to health message development that relies on user-generated content available on open-content platforms as a source of health messages.</p><p><strong>Objective: </strong>We examined the acceptability of user-generated content curated from Twitter (subsequently rebranded X) as a source of health support messages in a newly developed smoking cessation mobile intervention called Quit Journey and the optimal timing and frequency with which health messages can be deployed to support app users in real time.</p><p><strong>Methods: </strong>A total of 12 semistructured focus groups were held with 38 young adults with low socioeconomic status who smoked cigarettes, wanted to quit, and were aged 18 to 29 years. Focus groups were held virtually on GoTo Meeting, audio recorded, and transcribed verbatim. Deductive thematic analysis was used, with themes based on 5 constructs from the second unified theory of acceptance and use of technology (ie, effort expectancy, facilitating conditions, hedonic motivation, performance expectancy, and social influence) and negative, neutral, and positive sentiment.</p><p><strong>Results: </strong>Participants perceived user-generated content positively (56/108, 51.9% of the quotes) and focused on their perceived usefulness (37/108, 34.3% of the quotes). User-generated content was perceived as authentic, nonrepetitive support from people with similar real-life experiences. Negative or sarcastic user-generated content elicited negative reactions from participants. Participants preferred receiving 3 or fewer daily messages, ideally before cravings. Suggestions focused on the need to screen user-generated content before its inclusion in the app library and allow app users to customize message frequency and timing.</p><p><strong>Conclusions: </strong>User-generated content was deemed an acceptable source of health messages. This content can improve the efficacy and effectiveness of smoking cessation interventions by increasing their pool of unique messages that may be better received and more persuasive than expert-curated content. User-generated content can be used to curate health messages for all medical conditions and behaviors with relevant publicly available online content for integration in behavioral interventions given its high volume, brevity, and narrative-like nature. Future research is needed to investigate the effects of user-generated content on health behaviors and identify the theoretical mechanisms for these effects.</p>","PeriodicalId":36351,"journal":{"name":"JMIR Human Factors","volume":"12 ","pages":"e76804"},"PeriodicalIF":3.0,"publicationDate":"2025-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12711135/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145776117","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
Use of the ME-BYO Index, a Mobile Health App, During an Online Strength Training Program in Adults: Fidelity, Feasibility, and Acceptability Study. 在成人在线力量训练计划中使用移动健康应用ME-BYO指数:保真度、可行性和可接受性研究
IF 3 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-12-16 DOI: 10.2196/63123
Yoshinobu Saito, Naoki Kikuchi, Kaname Watanabe, Sho Nakamura, Hiroto Narimatsu
<p><strong>Background: </strong>Although various apps have been developed to support health behaviors, they are mostly commercial, possibly limiting the number of users. The ME-BYO index was developed by Kanagawa Prefecture in 2019 to comprehensively and numerically measure and visualize an individual's current health status and future disease risk by quantifying data. The ME-BYO index is free of charge, so it can be made available to as many prefectural residents as possible for health promotion. Effective online strength training programs are being developed that, when combined with ME-BYO index measurements, will help with both exercise habits and health management.</p><p><strong>Objective: </strong>In this study, we aimed to validate the fidelity, feasibility, and acceptability of self-measurement using the ME-BYO index during the implementation of an online strength training program.</p><p><strong>Methods: </strong>Participants were 23 adults aged 40 years or older who did not regularly perform muscle strengthening exercises. The strength training program was performed twice a week for 8 weeks (16 sessions in total), and the ME-BYO index was explained to the participants so that they could self-measure the ME-BYO index with a smartphone on the day of the strength training program, before its implementation. The ME-BYO index during the study period was continuously collected from the app, and the ME-BYO index adherence rate was calculated. Questionnaires were used to assess the feasibility (difficulty of measurement and motivation to improve lifestyle) and acceptability (intention to maintain measurement and appropriate frequency of measurement) of implementing and continuing the ME-BYO index measurements. Changes in the ME-BYO index between the first and second halves of the program period, examination of items strongly related to changes in the ME-BYO index, and a comparison of physical fitness and health outcomes before and after the program period were conducted.</p><p><strong>Results: </strong>The mean ME-BYO index adherence rate during the strength training program was 89.4% (SD 17%). Regarding acceptability, the participants were highly motivated to continue measuring the ME-BYO index (77%), and the appropriate frequency of measurement was once a week and twice a week (31% and 31%, respectively). Panel data analysis of the self-measured ME-BYO index showed no significant change in the ME-BYO index score; however, it increased to a higher score. Examination of the items that increased the overall score indicated that systolic blood pressure, mental resilience, and Mini-Cog scores were the relevant factors. The pre- and postprogram measurements showed no significant changes in items other than physical fitness.</p><p><strong>Conclusions: </strong>The fidelity, feasibility, and acceptability of measuring the ME-BYO index during a regular online strength training program were high, suggesting that self-measurement of the ME-BYO index could
背景:虽然已经开发了各种应用程序来支持健康行为,但它们大多是商业性的,可能限制了用户的数量。ME-BYO指数由神奈川县于2019年开发,旨在通过量化数据全面、数字化地衡量和可视化个人目前的健康状况和未来的疾病风险。ME-BYO指数是免费的,因此可以向尽可能多的县居民提供,以促进健康。有效的在线力量训练项目正在开发中,当与ME-BYO指数测量相结合时,将有助于锻炼习惯和健康管理。目的:在本研究中,我们旨在验证ME-BYO指数在实施在线力量训练计划过程中自我测量的保真度、可行性和可接受性。方法:参与者是23名年龄在40岁或以上的成年人,他们不经常进行肌肉强化锻炼。力量训练计划每周进行两次,共进行8周(共16次),并向参与者解释ME-BYO指数,以便他们在力量训练计划实施前用智能手机自行测量ME-BYO指数。在app中连续收集研究期间的ME-BYO指数,并计算ME-BYO指数依从率。采用问卷法评估ME-BYO指数测量实施和持续的可行性(测量难度和改善生活方式的动机)和可接受性(维持测量的意愿和适当的测量频率)。对项目前半期和后半期ME-BYO指数的变化、对与ME-BYO指数变化密切相关的项目的检查以及项目前后体质和健康结果的比较进行了研究。结果:力量训练期间ME-BYO指数的平均依从率为89.4% (SD为17%)。在可接受性方面,参与者有很高的动机继续测量ME-BYO指数(77%),适当的测量频率为每周一次和每周两次(分别为31%和31%)。自测ME-BYO指数面板数据分析显示,ME-BYO指数得分无显著变化;然而,它增加到更高的分数。对提高总分的项目的检查表明,收缩压、心理弹性和Mini-Cog评分是相关因素。节目前和节目后的测量结果显示,除了身体素质外,其他项目没有显著变化。结论:在常规网络力量训练项目中测量ME-BYO指数具有较高的保真度、可行性和可接受性,提示自我测量ME-BYO指数可用于实施和维持健康行为。这些发现表明,ME-BYO指数可以被推荐为一款基本的健康应用。
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引用次数: 0
Multiple Large Language Models' Performance on the Chinese Medical Licensing Examination: Quantitative Comparative Study. 多种大语言模型在中医执业资格考试中的表现:定量比较研究。
IF 3 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-12-16 DOI: 10.2196/77978
Yanyu Diao, Mengyuan Wu, Jingwen Xu, Yifeng Pan
<p><strong>Background: </strong>ChatGPT excels in natural language tasks, but its performance in the Chinese National Medical Licensing Examination (NMLE) and Chinese medical education remains underexplored. Meanwhile, Chinese corpus-based large language models (LLMs) such as ERNIE Bot, Tongyi Qianwen, Doubao, and DeepSeek have emerged, yet their effectiveness in the NMLE awaits systematic evaluation.</p><p><strong>Objective: </strong>This study aimed to quantitatively compare the performance of 6 LLMs (GPT-3.5, GPT-4, ERNIE Bot, Tongyi Qianwen, Doubao, and DeepSeek) in answering NMLE questions from 2018 to 2024 and analyze their feasibility as supplementary tools in Chinese medical education.</p><p><strong>Methods: </strong>We selected questions from the 4 content units of the NMLE's General Written test (2018-2024), preprocessed image- and table-based content into standardized text, and input the questions into each model. We evaluated the accuracy, comprehensiveness, and logical coherence of the responses, with quantitative comparison centered on scores and accuracy rates against the official answer keys (passing score: 360/600).</p><p><strong>Results: </strong>GPT-4 outperformed GPT-3.5 across all units, achieving average accuracies of 66.57% (SD 3.21%; unit 1), 69.05% (SD 2.87%; unit 2), 71.71% (SD 2.53%; unit 3), and 80.67% (SD 2.19%; unit 4), with consistent scores above the passing threshold. Among the Chinese models, DeepSeek demonstrated the highest overall performance, with an average score of 454.8 (SD 17.3) and average accuracies of 73.2% (unit 1, SD 2.89%) and 71.5% (unit 3, SD 2.64%), as well as average accuracies of 70.3% (unit 2, SD 3.02%) and 78.2% (unit 4, SD 2.47%). ERNIE Bot (mean score 442.3, SD 19.6; unit 1 accuracy =70.8%, SD 3.01%; unit 2 accuracy =68.7%, SD 3.15%; unit 3 accuracy =69.1%, SD 2.93%; unit 4 accuracy =68.3%, SD 2.76%), Tongyi Qianwen (mean score 426.5, SD 21.4; unit 1 accuracy =67.4%, SD 3.22%; unit 2 accuracy =65.9%, SD 3.31%; unit 3 accuracy =66.2%, SD 3.08%; unit 4 accuracy =67.2%, SD 2.89%), and Doubao (mean score 413.7, SD 23.1; unit 1 accuracy =65.2%, SD 3.45%; unit 2 accuracy =63.8%, SD 3.52%; unit 3 accuracy =64.1%, SD 3.27%; unit 4 accuracy =62.8%, SD 3.11%) all exceeded the passing score. DeepSeek's overall average accuracy (75.8%, SD 2.73%) was significantly higher than those of the other Chinese models (χ²₁=11.4, P=.001 vs ERNIE Bot; χ²₁=28.7, P<.001 vs Tongyi Qianwen; χ²₁=45.3, P<.001 vs Doubao). GPT-4's overall average accuracy (77.0%, SD 2.58%) was slightly higher than that of DeepSeek but not statistically significant (χ²₁=2.2, P=.14), while both outperformed GPT-3.5 (overall accuracy =68.5%, SD 3.67%; χ²₁=89.8, P<.001 for GPT-4 vs GPT-3.5; χ²₁=76.3, P<.001 for DeepSeek vs GPT-3.5).</p><p><strong>Conclusions: </strong>GPT-4 and Chinese-developed LLMs such as DeepSeek show potential as supplementary tools in Chinese medical education given their solid performance on the NMLE. However, further
背景:ChatGPT在自然语言任务中表现优异,但在中国国家医师执业资格考试(NMLE)和中国医学教育中的表现仍有待探索。与此同时,基于中文语料库的大型语言模型(llm)如ERNIE Bot、同义字文、豆包和DeepSeek已经出现,但它们在NMLE中的有效性有待系统评估。目的:本研究旨在定量比较2018 - 2024年6款法学硕士(GPT-3.5、GPT-4、ERNIE Bot、同医千文、豆宝、DeepSeek)在NMLE答题中的表现,分析其作为中国医学教育辅助工具的可行性。方法:从NMLE普通笔试(2018-2024)的4个内容单元中选取问题,将基于图像和表格的内容预处理为标准化文本,并将问题输入到每个模型中。我们对回答的准确性、全面性和逻辑连贯性进行了评估,并对官方答案的得分和准确率进行了定量比较(通过分数:360/600)。结果:GPT-4在所有单元中均优于GPT-3.5,平均准确率分别为66.57% (SD 3.21%;单元1)、69.05% (SD 2.87%;单元2)、71.71% (SD 2.53%;单元3)和80.67% (SD 2.19%;单元4),均高于合格阈值。在中文模型中,DeepSeek表现出最高的综合性能,平均得分为454.8 (SD 17.3),平均准确率为73.2%(单元1,SD 2.89%)和71.5%(单元3,SD 2.64%),平均准确率为70.3%(单元2,SD 3.02%)和78.2%(单元4,SD 2.47%)。厄尼Bot(平均得分442.3,SD 19.6;单位1精度= 70.8%,SD 3.01%;单位2精度= 68.7%,SD 3.15%;第三单元精度= 69.1%,SD 2.93%;单位4精度= 68.3%,SD 2.76%),统一任命(平均得分426.5,标准差21.4;单位1精度= 67.4%,SD 3.22%;单位2精度= 65.9%,SD 3.31%;第三单元精度= 66.2%,SD 3.08%;单位4精度= 67.2%,SD 2.89%),和Doubao(平均得分413.7,标准差23.1;单位1精度= 65.2%,SD 3.45%;单位2精度= 63.8%,SD 3.52%;第三单元精度= 64.1%,SD 3.27%;单元4准确度=62.8%,标准差3.11%)均超过及格。DeepSeek的总体平均准确率(75.8%,SD 2.73%)显著高于其他中国模型(χ²₁=11.4,P= 0.001 vs ERNIE Bot; χ²₁=28.7,P)。结论:GPT-4和中国开发的llm(如DeepSeek)在NMLE上表现出色,显示出作为中国医学教育补充工具的潜力。然而,复杂的推理、多模态处理和动态知识更新需要进一步优化,人类医学专业知识仍然是临床实践和教育的核心。
{"title":"Multiple Large Language Models' Performance on the Chinese Medical Licensing Examination: Quantitative Comparative Study.","authors":"Yanyu Diao, Mengyuan Wu, Jingwen Xu, Yifeng Pan","doi":"10.2196/77978","DOIUrl":"10.2196/77978","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;ChatGPT excels in natural language tasks, but its performance in the Chinese National Medical Licensing Examination (NMLE) and Chinese medical education remains underexplored. Meanwhile, Chinese corpus-based large language models (LLMs) such as ERNIE Bot, Tongyi Qianwen, Doubao, and DeepSeek have emerged, yet their effectiveness in the NMLE awaits systematic evaluation.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;This study aimed to quantitatively compare the performance of 6 LLMs (GPT-3.5, GPT-4, ERNIE Bot, Tongyi Qianwen, Doubao, and DeepSeek) in answering NMLE questions from 2018 to 2024 and analyze their feasibility as supplementary tools in Chinese medical education.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;We selected questions from the 4 content units of the NMLE's General Written test (2018-2024), preprocessed image- and table-based content into standardized text, and input the questions into each model. We evaluated the accuracy, comprehensiveness, and logical coherence of the responses, with quantitative comparison centered on scores and accuracy rates against the official answer keys (passing score: 360/600).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;GPT-4 outperformed GPT-3.5 across all units, achieving average accuracies of 66.57% (SD 3.21%; unit 1), 69.05% (SD 2.87%; unit 2), 71.71% (SD 2.53%; unit 3), and 80.67% (SD 2.19%; unit 4), with consistent scores above the passing threshold. Among the Chinese models, DeepSeek demonstrated the highest overall performance, with an average score of 454.8 (SD 17.3) and average accuracies of 73.2% (unit 1, SD 2.89%) and 71.5% (unit 3, SD 2.64%), as well as average accuracies of 70.3% (unit 2, SD 3.02%) and 78.2% (unit 4, SD 2.47%). ERNIE Bot (mean score 442.3, SD 19.6; unit 1 accuracy =70.8%, SD 3.01%; unit 2 accuracy =68.7%, SD 3.15%; unit 3 accuracy =69.1%, SD 2.93%; unit 4 accuracy =68.3%, SD 2.76%), Tongyi Qianwen (mean score 426.5, SD 21.4; unit 1 accuracy =67.4%, SD 3.22%; unit 2 accuracy =65.9%, SD 3.31%; unit 3 accuracy =66.2%, SD 3.08%; unit 4 accuracy =67.2%, SD 2.89%), and Doubao (mean score 413.7, SD 23.1; unit 1 accuracy =65.2%, SD 3.45%; unit 2 accuracy =63.8%, SD 3.52%; unit 3 accuracy =64.1%, SD 3.27%; unit 4 accuracy =62.8%, SD 3.11%) all exceeded the passing score. DeepSeek's overall average accuracy (75.8%, SD 2.73%) was significantly higher than those of the other Chinese models (χ²₁=11.4, P=.001 vs ERNIE Bot; χ²₁=28.7, P&lt;.001 vs Tongyi Qianwen; χ²₁=45.3, P&lt;.001 vs Doubao). GPT-4's overall average accuracy (77.0%, SD 2.58%) was slightly higher than that of DeepSeek but not statistically significant (χ²₁=2.2, P=.14), while both outperformed GPT-3.5 (overall accuracy =68.5%, SD 3.67%; χ²₁=89.8, P&lt;.001 for GPT-4 vs GPT-3.5; χ²₁=76.3, P&lt;.001 for DeepSeek vs GPT-3.5).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;GPT-4 and Chinese-developed LLMs such as DeepSeek show potential as supplementary tools in Chinese medical education given their solid performance on the NMLE. However, further ","PeriodicalId":36351,"journal":{"name":"JMIR Human Factors","volume":"12 ","pages":"e77978"},"PeriodicalIF":3.0,"publicationDate":"2025-12-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12707437/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145769344","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
Enhancing Safety in Clinical Practice: Cross-Sectional, Within-Subjects, Simulated-Use Compliance Study Using BD PosiFlush SafeScrub. 增强临床实践中的安全性:一项使用BD PosiFlush™SafeScrub的横断面、受试者内、模拟使用依从性研究。
IF 3 Q2 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-12-15 DOI: 10.2196/78967
Kyle De Boer, John Simpson, Purnima Sharma, Trevor J Steele

Background: Needleless access devices are essential for intravenous therapy but can be a source of contamination and catheter-related bloodstream infections (CRBSIs) if not disinfected properly. The BD PosiFlush SafeScrub (Becton, Dickinson and Company) is designed to support aseptic nontouch technique (ANTT) by incorporating a built-in reminder to "scrub-the-hub" before flushing. This feature can help improve compliance with disinfection practices and may reduce the risk of microbial contamination.

Objective: This study aimed to evaluate compliance with scrubbing before flushing using the BD PosiFlush SafeScrub in a simulated clinical environment compared with standard disinfection and flushing practices (alcohol swabs and prefilled saline syringes).

Methods: A cross-sectional, within-subjects, simulated-use compliance study was conducted with health care professionals familiarized with BD PosiFlush SafeScrub (a prefilled BD PosiFlush Syringe with an integrated disinfecting unit). Compliance was defined according to the disinfection procedure specified for each scenario; participants were considered compliant with standard practice if they followed their own institutional policy (ranging from 5 to 30 seconds or based on stroke counts), while compliance with BD PosiFlush SafeScrub required scrubbing for at least 10 seconds with a minimum of 8 clockwise and 8 counterclockwise rotations, in accordance with the instructions for use (IFU). Compliance with disinfection was monitored and recorded for both the BD PosiFlush SafeScrub and standard disinfection and flushing practice.

Results: Compliance with catheter hub disinfection was assessed among 60 participants for BD PosiFlush SafeScrub and 57 participants for standard practice. During preaccess procedures (Flush 1), BD PosiFlush SafeScrub achieved 46% compliance versus 21% with standard practice, representing an absolute improvement of 25% and a 119% relative improvement (P<.001). During the postmedication procedure (Flush 2), compliance was 22% with BD PosiFlush SafeScrub compared with 13% for standard practice, corresponding to a 9% absolute improvement and 69% relative improvement, although not statistically significant (P=.12). Overall, the compliance rate was 34% (81/240 interactions) in the BD PosiFlush SafeScrub group compared with 17% (39/228 interactions) in the standard practice group, representing an absolute improvement of 17% and a relative improvement of 100% (P<.001).

Conclusions: The BD PosiFlush SafeScrub, with its integrated disinfection unit, yielded approximately double the scrub-the-hub compliance (34%) before flushing compared to the standard practice of alcohol pads and prefilled saline syringes (17%), supporting its role in facilitating adherence to ANTT, which may reduce microbial growth.

背景:无针接触装置是静脉治疗必不可少的,但如果消毒不当,可能成为污染源和导管相关性血流感染(CRBSIs)。BD PosiFlush™SafeScrub旨在支持无菌非接触技术(ANTT®),在冲洗前包含内置提醒“擦洗中心”。这一特性有助于提高消毒操作的合规性,并可能降低微生物污染的风险。目的:本研究的目的是评估在模拟临床环境中使用BD PosiFlush SafeScrub冲洗前擦洗的依从性,并与标准消毒和冲洗方法(酒精拭子和预充盐水注射器)进行比较。方法:在熟悉BD PosiFlush SafeScrub(带集成消毒单元的预充BD PosiFlush注射器)的医疗保健专业人员中进行了一项横断面、受试者内部、模拟使用依从性研究。根据每种情况指定的消毒程序定义合规性,如果参与者遵循自己的机构政策(范围从5-30秒或基于中风计数),则认为符合标准做法,而符合BD PosiFlush SafeScrub要求洗涤至少10秒,至少顺时针旋转8次和逆时针旋转8次,根据IFU。监测和记录了BD PosiFlush安全擦洗和标准消毒和冲洗操作的消毒依从性。结果:60名BD PosiFlush SafeScrub参与者和57名标准实践参与者对导管中心消毒的依从性进行了评估。在访问前程序(冲洗1)中,BD PosiFlush SafeScrub达到46%的依从性,而标准实践为21%,代表绝对改善25%,相对改善119% (P < 0.001)。在给药后程序(冲洗2)中,BD PosiFlush SafeScrub的依从性为22%,而标准实践的依从性为13%,对应于9%的绝对改善和69%的相对改善,尽管没有统计学意义(P = .12)。总体而言,BD PosiFlush SafeScrub组的依从率为34%(240次相互作用中有81次),而标准实践组的依从率为17%(228次相互作用中有39次),绝对改善为17%,相对改善为100% (P < 0.001)。结论:与酒精垫和预充盐水注射器的标准做法(17%)相比,带有集成消毒单元的BD PosiFlush safesscrub在冲洗前的擦洗中心依从性(34%)约为两倍,支持其在促进对ANTT®的依从性方面的作用,这可能会减少微生物的生长。临床试验:
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引用次数: 0
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JMIR Human Factors
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