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Exploring Feature Priorities and User Needs in Developing Virtual Study Assistants. 探索开发虚拟学习助手的功能优先级和用户需求。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-03-06 DOI: 10.2196/86945
Chi-Shan Tsai, HyunHae Lee, Warren Szewczyk, Julia K Palmer, Sophie Putnam, Sean A Munson, Jaimee L Heffner, Alexi Vasbinder, Amandalynne Paullada, Weichao Yuwen, Kerryn W Reding

This formative research explored health science researchers' perspectives on the development of an artificial intelligence-based virtual study assistant and identified 8 potential features and their priorities.

这项形成性研究探讨了健康科学研究人员对开发基于人工智能的虚拟学习助手的看法,并确定了8个潜在特征及其优先事项。
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引用次数: 0
Knowledge graphs based on meta-analysis papers improve the quality of case formulation: a mixed methods design. 基于元分析论文的知识图谱提高了案例表述的质量:一种混合方法设计。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-03-06 DOI: 10.2196/76808
Kenji Yokotani, Yasumitsu Jikihara, Kohei Koiwa

Background: Case formulation (CF) is a core skill for therapists; however, creating high-quality CF requires considerable time.

Objective: This study demonstrates that providing a knowledge graph based on the meta-analytic literature can enhance CF quality.

Methods: Five groups were established, including four large language model (LLM) groups and one human expert group, each generating 25 CFs based on 25 vignettes. The Control group with Claude Sonnet 3.7 produced 25 CFs. The Personalization group served as the control group with additional personalization prompts. The Knowledge Graph group employed an LLM that generated 25 CFs, which was provided with a meta-analysis Knowledge Graph. Further incorporation of additional personalization prompts then comprised the Knowledge Graph with Personalization group. Finally, the Expert Group consisted of 25 CFs generated by a human expert. These 125 CFs in total were evaluated for general quality (i.e., correctness, completeness, feasibility, and consistency) using a 7-point scale and 18 essential elements with binary scores (0 or 1) by another human expert. The CFs were also qualitatively analyzed.

Results: The Knowledge Graph and Knowledge Graph with Personalization groups scored significantly higher than the control group in terms of correctness, completeness, and feasibility. The Expert group scored significantly higher on consistency than the machine-generated groups. Additionally, there was no significant difference in the feasibility scores between the Knowledge Graph, Knowledge Graph with Personalization, and expert groups. The qualitative evaluation suggested that human CFs narrow the text to content that is easy for the client to read, whereas machine CFs are more likely to include expressions that are unnatural to the client.

Conclusions: These results indicate that providing knowledge graphs to novice therapists increases the correctness, completeness, and feasibility of CF. Providing experienced therapists with knowledge graphs is suggested to improve the quality of their CF and mental health services.

Clinicaltrial: None.

背景:案例制定(CF)是治疗师的核心技能;然而,创建高质量的CF需要大量的时间。目的:本研究表明,提供基于元分析文献的知识图谱可以提高CF质量。方法:建立5个小组,包括4个大型语言模型组(LLM)和1个人类专家组,每组基于25个小片段生成25个cf。使用Claude Sonnet 3.7的对照组产生25个CFs。Personalization组作为具有其他个性化提示的控制组。知识图谱组使用了一个法学硕士,生成了25个cf,并提供了一个元分析知识图谱。进一步整合额外的个性化提示,然后组成了个性化知识图谱组。最后,专家组由一名人类专家生成的25个cf组成。这125个cf的总体质量(即正确性、完整性、可行性和一致性)由另一位人类专家使用7分制和18个基本要素(二进制分数为0或1)进行评估。对CFs也进行了定性分析。结果:知识图谱组和个性化知识图谱组在正确性、完整性和可行性方面均显著高于对照组。专家组在一致性方面的得分明显高于机器生成组。此外,知识图谱、个性化知识图谱和专家组在可行性得分上没有显著差异。定性评估表明,人类的CFs将文本缩小到客户端易于阅读的内容,而机器CFs更有可能包含对客户端不自然的表达式。结论:向新手治疗师提供知识图谱可以提高CF的正确性、完整性和可行性,建议向经验丰富的治疗师提供知识图谱,以提高其CF和心理健康服务的质量。临床试验:没有。
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引用次数: 0
Assessment of Emerging Technologies to Support Individuals With At-Risk Alcohol Consumption: Pilot Controlled Investigation Study. 对支持高危饮酒个体的新兴技术的评估:试点对照调查研究
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-03-06 DOI: 10.2196/83592
Karl Andersson, Linda Handlin, Sanela Huskic Beslic, Rajna Knez, Afrouz Behboudi, Marie Wilhsson

Background: The Swedish National Board of Health and Welfare recently updated the national guidelines for at-risk consumption of alcohol. Nearly 30% of the Swedish population now falls under the at-risk category and should be provided with support.

Objective: This project aims to identify and evaluate efficient, scalable tools to support individuals with risk-prone alcohol consumption. The project seeks to explore innovative, accessible technologies that could be implemented in large-scale public health interventions.

Methods: A pilot-scale clinical study was conducted to assess the feasibility of using emerging technologies for this purpose. Eight healthy volunteers participated in controlled alcohol consumption while being monitored through 2 methods: an eye-scanning tool integrated into a standard mobile phone and saliva sampling for biomarkers such as serotonin and orexin.

Results: Eye-scanning parameters began to shift in some participants at approximately 0.4 to 0.5 per mille blood alcohol concentration, particularly in the form of impaired eye convergence. Furthermore, at around 0.5 per mille, participants encountered practical difficulties in managing the eye-scanning app. Salivary biomarkers did not show any clear correlation with alcohol intake, presumably due to the low number of participants. Beyond biological findings, the study also generated important procedural insights for designing a large-scale clinical study.

Conclusions: Eye scanning showed potential as a noninvasive and accessible method for detecting and monitoring moderate alcohol consumption effects, while serotonin and orexin biomarkers were not informative in this context. On the basis of these findings and procedural learnings, eye-scanning tools warrant further investigation in larger clinical studies aimed at developing scalable support for risk-prone alcohol consumption.

背景:瑞典国家健康和福利委员会最近更新了国家高危饮酒指南。近30%的瑞典人现在属于高危人群,应该得到支持。目的:本项目旨在确定和评估有效的、可扩展的工具,以支持有饮酒风险的个人。该项目旨在探索可在大规模公共卫生干预措施中实施的可获得的创新技术。方法:进行了一项中试规模的临床研究,以评估在此目的中使用新兴技术的可行性。8名健康志愿者参与了控制饮酒的研究,同时通过两种方法进行监测:一种是集成在标准手机中的眼睛扫描工具,另一种是唾液中血清素和食欲素等生物标志物的采样。结果:在一些参与者中,当血液酒精浓度约为每英里0.4至0.5时,眼睛扫描参数开始发生变化,尤其是在眼睛收敛受损的情况下。此外,在每英里0.5左右,参与者在管理眼睛扫描应用程序时遇到了实际困难。唾液生物标志物没有显示出与酒精摄入量有任何明确的相关性,可能是由于参与者人数少。除了生物学上的发现,这项研究还为设计大规模临床研究提供了重要的程序见解。结论:眼扫描作为一种检测和监测中度酒精消耗效应的无创、可及的方法具有潜力,而血清素和食欲素生物标志物在此背景下没有提供信息。在这些发现和程序学习的基础上,眼扫描工具值得在更大规模的临床研究中进一步调查,旨在为易患风险的酒精消费提供可扩展的支持。
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引用次数: 0
Transportation as a Barrier to Health Care Access Among Patients With Knee Arthritis: Cross-Sectional Study. 交通是膝关节关节炎患者获得医疗保健的障碍:横断面研究。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-03-06 DOI: 10.2196/91207
Erin Youn, James Chen

Unlabelled: This study uses the 2011-2017 National Health Interview Survey (NHIS) data to demonstrate that sociodemographic factors are associated with transportation delays among individuals with knee osteoarthritis.

未标记:本研究使用2011-2017年全国健康访谈调查(NHIS)数据来证明社会人口因素与膝关节骨关节炎患者的交通延误有关。
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引用次数: 0
Empowering Informal Caregivers of Persons With Early-Stage Dementia by Large Language Models: Mixed Methods Evaluation. 通过大语言模型赋予早期痴呆患者非正式照顾者权力:混合方法评估。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-03-05 DOI: 10.2196/79975
Huayu Zhou, Ziwei Zhu, Kyeung Mi Oh, Sungsoo Ray Hong
<p><strong>Background: </strong>Acquiring relevant knowledge and support is essential for informal caregivers of persons with early-stage dementia, including awareness, access, and use of comprehensive resources for both persons with dementia and caregiver support. With appropriate strategies and early-stage support, informal caregivers can play a vital role in enhancing the well-being of persons with dementia and potentially slowing their progression. While large language models (LLMs) can provide easy access to caregiving knowledge, the risks, perceived challenges, and ways to improve LLM-generated responses in practice remain underexplored.</p><p><strong>Objective: </strong>In this study, we aim to (1) examine the risks and perceived challenges of using a baseline ChatGPT-4o, an internet-accessible artificial intelligence model, for dementia caregiving support and (2) understand how an enhanced version of ChatGPT-4o, equipped with up-to-date dementia caregiving knowledge, can mitigate these risks and challenges.</p><p><strong>Methods: </strong>We compiled 32 representative questions from informal caregivers seeking guidance on early-stage dementia. We developed two ChatGPT-4o conditions: C1, the publicly available baseline model, and C2, an experimental version enhanced through prompt engineering and grounded in a conceptual framework-drawn from health science and gerontology literature-to empower caregivers of individuals with early-stage dementia. Using these conditions, we generated 64 responses (32 pairs) to the questions. Twelve experts evaluated them with validated tools assessing accuracy, reasoning, clarity, usefulness, trust, satisfaction, safety, harm, and relevance. A Mann-Whitney U test compared the conditions. After the survey, we conducted interviews to explore experts' perceived differences, remaining challenges, and design opportunities. Interviews were transcribed and analyzed using descriptive thematic analysis.</p><p><strong>Results: </strong>Responses in C2 showed significant improvements in 3 criteria-actionability, relevance, and perceived satisfaction-compared to C1. However, no significant differences were found in the remaining 5 criteria: response accuracy, the model's ability to understand the question, intelligibility, trustworthiness, response safety, and perceived harm. Qualitative analysis of interviews revealed two key insights: (1) differences between baseline and experimental responses and (2) possible reasons for these differences. Twelve experts evaluated wordiness, detail, empathy, satisfaction, accuracy, relevance, and bias. Both models were considered somewhat verbose, but the experimental model's responses were viewed as more detailed, relevant, and actionable. Accuracy appeared similar across models, yet participants reported greater satisfaction with the experimental model's outputs.</p><p><strong>Conclusions: </strong>Results indicate that both conditions generated responses perceived as reasonable an
背景:获得相关知识和支持对于早期痴呆症患者的非正式照护者至关重要,包括对痴呆症患者和照护者支持的全面资源的认识、获取和使用。通过适当的战略和早期支持,非正式护理人员可以在增进痴呆症患者的福祉和可能减缓其进展方面发挥至关重要的作用。虽然大型语言模型(llm)可以方便地访问护理知识,但风险、感知到的挑战以及在实践中改进llm生成的响应的方法仍未得到充分探索。目的:在本研究中,我们的目标是(1)检查使用基线chatgpt - 40(一种可访问互联网的人工智能模型)进行痴呆症护理支持的风险和感知挑战;(2)了解配备最新痴呆症护理知识的增强版chatgpt - 40如何减轻这些风险和挑战。方法:我们从寻求早期痴呆指导的非正式护理人员中收集了32个具有代表性的问题。我们开发了两个chatgpt - 40条件:C1,公开可用的基线模型,C2,通过快速工程增强的实验版本,并以健康科学和老年学文献为基础的概念框架为基础,以增强早期痴呆症患者的护理人员的能力。使用这些条件,我们生成了64个问题的回答(32对)。12位专家使用经过验证的工具对其进行评估,评估准确性、推理性、清晰度、有用性、信任、满意度、安全性、危害和相关性。一项曼-惠特尼测试比较了这两种情况。调查结束后,我们进行了访谈,以探讨专家的感知差异,剩下的挑战和设计机会。访谈记录和分析使用描述性专题分析。结果:与C1组相比,C2组的反应在可操作性、相关性和感知满意度3个标准上有显著改善。然而,在其余5个标准上没有发现显著差异:反应准确性、模型理解问题的能力、可理解性、可信度、反应安全性和感知伤害。访谈的定性分析揭示了两个关键的见解:(1)基线和实验反应之间的差异;(2)这些差异的可能原因。12位专家评估了冗长、细节、同理心、满意度、准确性、相关性和偏见。两种模型都被认为有些冗长,但实验模型的反应被认为更详细、相关和可操作。各模型的准确性似乎相似,但参与者对实验模型的输出更满意。结论:结果表明,两种情况下产生的反应被认为是合理的和可理解的。然而,实验模型在护理需求方面提供了更相关、更实用的指导,提供了与32个测试问题和可操作建议相一致的具体信息。与基线模型相比,这导致了更高的感知满意度。
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引用次数: 0
Health-Related Quality of Life Before and After Sobriety in Combination With an Adjunctive Journaling App in Patients With Alcohol-Related Liver Disease: Prospective Single-Arm Study. 酒精相关性肝病患者在清醒前后与健康相关的生活质量结合辅助日志应用程序:前瞻性单组研究
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-03-05 DOI: 10.2196/80421
Noriyo Yamashiki, Noriko Kudo, Kyoko Kawabata, Takako Fujimaki, Eiji Aramaki, Miki Murata, Shunichiro Ikeda, Hiroko Yoshii, Hisako Yamada, Makoto Naganuma
<p><strong>Background: </strong>Alcohol-related liver disease (ALD) is a global health concern, and harmful alcohol use negatively affects clinical outcomes and health-related quality of life (HRQOL). Previous studies have demonstrated impaired HRQOL in chronic liver disease, including ALD; however, evidence remains limited regarding whether hepatologist-delivered abstinence support in outpatient practice can improve HRQOL. Digital interventions such as smartphone journaling apps may support behavior change, but their effectiveness in hepatology-led care settings has not been well established.</p><p><strong>Objective: </strong>This study aimed to prospectively evaluate changes in HRQOL over time among patients with ALD receiving routine hepatologist-led abstinence support supplemented by a smartphone-based journaling app.</p><p><strong>Methods: </strong>This was a prospective single-arm observational study. Eligibility criteria included a diagnosis of ALD, outpatient follow-up in hepatology, advice to abstain from alcohol, and written informed consent; patients were excluded if they reported abstinence for >1 year, had no intention to reduce or abstain from alcohol, or declined medical follow-up. In total, 21 outpatients with ALD (mean age 51, SD 3 years; men: n=12, 57.1%) were enrolled from a gastroenterology and hepatology outpatient clinic between August 2021 and July 2023 (convenience sampling). Participants attended scheduled visits at 4, 8, 12, and 24 weeks and received brief abstinence counseling by hepatologists while using a journaling app. HRQOL was assessed using the Japanese version of the 36-Item Short Form Health Survey version 2 at entry, week 8, and week 24. Changes in subscale and summary scores were analyzed using paired t tests (2-sided α=.05) with 95% CIs; when normality assumptions were not met, Wilcoxon signed-rank tests were applied.</p><p><strong>Results: </strong>From entry to week 8, significant improvements were observed in physical functioning (mean difference [MD] +4.70, 95% CI 1.62-7.78; P=.005), role physical (MD +7.87, 95% CI 1.05-14.70; P=.02), general health (MD +5.82, 95% CI 1.74-9.88; P=.007), and role emotional (MD +7.85, 95% CI 0.29-15.41; P=.04). The Physical Component Summary score also improved (MD +4.78, 95% CI 1.22-8.34; P=.01). These findings were consistent in sensitivity analysis using the Wilcoxon signed-rank test. No significant changes were observed in mental or social HRQOL domains. In subgroup analyses, patients who maintained abstinence during the first 8 weeks (7/21, 33.3%) showed continued improvement in physical HRQOL up to 24 weeks, whereas those who continued drinking (11/21, 52.4%) did not exhibit meaningful change.</p><p><strong>Conclusions: </strong>In this exploratory observational study, hepatologist-led abstinence support supplemented by a smartphone-based journaling app was associated with improvements in physical HRQOL. Unlike previous studies that have focused on addiction speciali
背景:酒精相关性肝病(ALD)是一个全球性的健康问题,有害的酒精使用会对临床结果和健康相关生活质量(HRQOL)产生负面影响。先前的研究表明慢性肝病患者的HRQOL受损,包括ALD;然而,关于在门诊实践中肝病学家提供的禁欲支持是否可以改善HRQOL的证据仍然有限。智能手机日志应用程序等数字干预措施可能支持行为改变,但它们在肝病学主导的护理环境中的有效性尚未得到很好的证实。目的:本研究旨在前瞻性评估接受常规肝病学家主导的戒断支持并辅以智能手机日志应用程序的ALD患者HRQOL随时间的变化。方法:这是一项前瞻性单臂观察性研究。入选标准包括ALD诊断、肝病门诊随访、戒酒建议和书面知情同意;如果患者报告戒酒10 - 10年,无意减少或戒酒,或拒绝医疗随访,则排除。在2021年8月至2023年7月期间,共有21名ALD门诊患者(平均年龄51岁,SD 3岁;男性:n=12,占57.1%)从胃肠病学和肝病学门诊入选(方便抽样)。参与者在第4、8、12和24周参加预定的访问,并在使用日志应用程序时接受肝病学家的简短戒断咨询。HRQOL在进入、第8周和第24周使用日本版的36项简短健康调查版本2进行评估。采用配对t检验分析亚量表和总结评分的变化(双侧α= 0.05), ci为95%;当不满足正态性假设时,应用Wilcoxon符号秩检验。结果:从入组到第8周,在身体功能(平均差值[MD] +4.70, 95% CI 1.62-7.78; P= 0.005)、角色身体(MD +7.87, 95% CI 1.05-14.70; P= 0.02)、一般健康(MD +5.82, 95% CI 1.74-9.88; P= 0.007)和角色情绪(MD +7.85, 95% CI 0.29-15.41; P= 0.04)方面观察到显著改善。Physical Component Summary评分也有改善(MD +4.78, 95% CI 1.22-8.34; P= 0.01)。这些发现在使用Wilcoxon符号秩检验的敏感性分析中是一致的。在心理或社会HRQOL领域未观察到显著变化。在亚组分析中,在前8周保持戒酒的患者(7/21,33.3%)的身体HRQOL持续改善至24周,而继续饮酒的患者(11/21,52.4%)没有表现出有意义的变化。结论:在这项探索性观察研究中,肝病学家主导的戒酒支持辅以基于智能手机的日志应用程序与身体HRQOL的改善有关。与以往专注于成瘾专家主导干预的研究不同,本研究评估了肝病学家在常规门诊实践中提供的戒断支持,提供了对数字支持方法的真实评估。这些发现表明,在获得专业成瘾服务的机会有限的临床环境中,由肝病学家领导的数字支持的护理可能是一种可行的策略。
{"title":"Health-Related Quality of Life Before and After Sobriety in Combination With an Adjunctive Journaling App in Patients With Alcohol-Related Liver Disease: Prospective Single-Arm Study.","authors":"Noriyo Yamashiki, Noriko Kudo, Kyoko Kawabata, Takako Fujimaki, Eiji Aramaki, Miki Murata, Shunichiro Ikeda, Hiroko Yoshii, Hisako Yamada, Makoto Naganuma","doi":"10.2196/80421","DOIUrl":"10.2196/80421","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;Alcohol-related liver disease (ALD) is a global health concern, and harmful alcohol use negatively affects clinical outcomes and health-related quality of life (HRQOL). Previous studies have demonstrated impaired HRQOL in chronic liver disease, including ALD; however, evidence remains limited regarding whether hepatologist-delivered abstinence support in outpatient practice can improve HRQOL. Digital interventions such as smartphone journaling apps may support behavior change, but their effectiveness in hepatology-led care settings has not been well established.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;This study aimed to prospectively evaluate changes in HRQOL over time among patients with ALD receiving routine hepatologist-led abstinence support supplemented by a smartphone-based journaling app.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;This was a prospective single-arm observational study. Eligibility criteria included a diagnosis of ALD, outpatient follow-up in hepatology, advice to abstain from alcohol, and written informed consent; patients were excluded if they reported abstinence for &gt;1 year, had no intention to reduce or abstain from alcohol, or declined medical follow-up. In total, 21 outpatients with ALD (mean age 51, SD 3 years; men: n=12, 57.1%) were enrolled from a gastroenterology and hepatology outpatient clinic between August 2021 and July 2023 (convenience sampling). Participants attended scheduled visits at 4, 8, 12, and 24 weeks and received brief abstinence counseling by hepatologists while using a journaling app. HRQOL was assessed using the Japanese version of the 36-Item Short Form Health Survey version 2 at entry, week 8, and week 24. Changes in subscale and summary scores were analyzed using paired t tests (2-sided α=.05) with 95% CIs; when normality assumptions were not met, Wilcoxon signed-rank tests were applied.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;From entry to week 8, significant improvements were observed in physical functioning (mean difference [MD] +4.70, 95% CI 1.62-7.78; P=.005), role physical (MD +7.87, 95% CI 1.05-14.70; P=.02), general health (MD +5.82, 95% CI 1.74-9.88; P=.007), and role emotional (MD +7.85, 95% CI 0.29-15.41; P=.04). The Physical Component Summary score also improved (MD +4.78, 95% CI 1.22-8.34; P=.01). These findings were consistent in sensitivity analysis using the Wilcoxon signed-rank test. No significant changes were observed in mental or social HRQOL domains. In subgroup analyses, patients who maintained abstinence during the first 8 weeks (7/21, 33.3%) showed continued improvement in physical HRQOL up to 24 weeks, whereas those who continued drinking (11/21, 52.4%) did not exhibit meaningful change.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;In this exploratory observational study, hepatologist-led abstinence support supplemented by a smartphone-based journaling app was associated with improvements in physical HRQOL. Unlike previous studies that have focused on addiction speciali","PeriodicalId":14841,"journal":{"name":"JMIR Formative Research","volume":"10 ","pages":"e80421"},"PeriodicalIF":2.0,"publicationDate":"2026-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13003206/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147365206","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
Cross-Cultural Differences in Public Discourse on COVID-19 Vaccination in the United States and South Korea: Cross-Sectional Analysis Using Natural Language Processing. 美国和韩国COVID-19疫苗接种公共话语的跨文化差异:使用自然语言处理的横断面分析
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-03-05 DOI: 10.2196/84791
Sangpil Youm, Sou Hyun Jang, Haewoon Kwak, Jaeyoung Choi, Yong Jeong Yi
<p><strong>Background: </strong>The COVID-19 vaccine was introduced as a crucial tool to combat the pandemic. However, concerns about its effectiveness, side effects, and misinformation spread remain. Prior research largely relied on survey-based approaches with limited populations. To address these limitations, social media offers a broader, more naturalistic lens into public discourse on COVID-19 vaccination. Accordingly, our study leverages social media data to identify factors shaping vaccine-related information needs, perceptions, and communication dynamics.</p><p><strong>Objective: </strong>This study investigated public discourse about COVID-19 vaccines on community-driven question-and-answer sites in the United States (Quora; Quora, Inc) and South Korea (Naver Knowledge-iN; Naver Corp) to identify cross-national similarities and differences in vaccine-related information needs, sentiment patterns, and public perceptions over time.</p><p><strong>Methods: </strong>We analyzed publicly available COVID-19 vaccine-related questions and answers posted between June 27, 2020, and June 27, 2021, on 2 community-driven question-and-answer platforms: Quora (United States) and Naver Knowledge-iN (South Korea). After preprocessing and sample-size matching, the dataset included 3952 question-answer pairs per platform, with one community-selected (most upvoted) answer analyzed per question. Natural language processing (NLP) techniques were applied for topic classification and sentiment analysis. Questions were categorized using a hybrid topic modeling approach combining Latent Dirichlet Allocation (LDA) and Top2Vec, identifying 5 topics on Quora and 7 topics on Naver Knowledge-iN. Answer sentiments were classified using an ensemble of Bidirectional Encoder Representations from Transformers (BERT; Google LLC)- and Efficiently Learning an Encoder that Classifies Token Replacements Accurately (ELECTRA; Google LLC)-based transformer models, and temporal sentiment trends were examined using monthly aggregation.</p><p><strong>Results: </strong>Five shared information needs emerged, including effects of vaccines, variants, government policy, visiting overseas, and different vaccines, while South Korea uniquely exhibited vaccination appointments (711/3952, 18%) and school and education (513/3592, 13%). Negative sentiment predominated in US (Quora) answers across 4 of 5 topics, whereas positive sentiment exceeded 50% (498/790, 337/474, 367/592, 218/316, 348/553, 562/711, and 364/513) across all 7 topics on Naver Knowledge-iN. Temporally, US sentiment exhibited multiple positive-negative crossovers, whereas Korean sentiment stabilized toward positivity after February 2021, coinciding with the national vaccine rollout. Question-answer sentiment pairs showed contrasting interaction patterns, including negative-negative pairs dominated in the United States (eg, 504/978, 51.5% for different vaccines), while in South Korea, positive-positive and negative-positive pairs
背景:COVID-19疫苗是抗击大流行的一项重要工具。然而,对其有效性、副作用和错误信息传播的担忧仍然存在。先前的研究主要依赖于基于调查的方法和有限的人口。为了解决这些限制,社交媒体为有关COVID-19疫苗接种的公共话语提供了一个更广泛、更自然的视角。因此,我们的研究利用社交媒体数据来确定影响疫苗相关信息需求、认知和沟通动态的因素。目的:本研究调查了美国(Quora; Quora, Inc .)和韩国(Naver Knowledge-iN; Naver Corp .)社区驱动的问答网站上关于COVID-19疫苗的公众话语,以确定不同国家在疫苗相关信息需求、情绪模式和公众认知方面的异同。方法:我们分析了2020年6月27日至2021年6月27日期间在两个社区驱动的问答平台:Quora(美国)和Naver Knowledge-iN(韩国)上发布的公开的COVID-19疫苗相关问题和答案。经过预处理和样本量匹配,该数据集包括每个平台3952对问答,每个问题分析一个社区选择(最多投票)的答案。采用自然语言处理(NLP)技术进行主题分类和情感分析。使用结合潜在狄利克雷分配(Latent Dirichlet Allocation, LDA)和Top2Vec的混合主题建模方法对问题进行分类,确定了Quora上的5个主题和Naver Knowledge-iN上的7个主题。使用来自变压器(BERT;谷歌LLC)的双向编码器表示的集合对回答情绪进行分类-以及高效学习基于变压器模型的编码器,该编码器准确分类令牌替换(ELECTRA;谷歌LLC),并使用每月汇总检查时间情绪趋势。结果:出现了5个共享信息需求,包括疫苗的效果、变异、政府政策、海外访问和不同的疫苗,而韩国独特地展示了疫苗接种预约(711/3952,18%)和学校和教育(513/3592,13%)。在美国(Quora)的5个主题中,负面情绪占主导地位,而在Naver Knowledge-iN的所有7个主题中,正面情绪超过50%(498/790、337/474、367/592、218/316、348/553、562/711和364/513)。从时间上看,美国的情绪出现了多次正负交叉,而韩国的情绪则在2021年2月接种疫苗后趋于积极。在韩国,7个主题中,阳性-阳性和负阳性对占比超过63%(498/790、337/474、367/592、218/316、348/553、562/711和364/513),除变异外,7个主题中有6个主题以阳性-阳性对最为普遍。结论:受文化背景、对政府的信任和信息寻求环境的影响,两国公众对COVID-19疫苗和相关信息需求的看法存在差异。对两国社会问答数据的分析显示,信息需求是共同的,但情绪模式是不同的。这些发现强调了社交媒体数据对公共卫生研究的价值,以及制定特定于文化和平台的传播策略的必要性。
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引用次数: 0
Online Social Support - an Adjunct or Substitute for Traditional Social Support: Cross-Sectional Study. 在线社会支持——传统社会支持的辅助或替代:横断面研究。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-03-05 DOI: 10.2196/90751
Ruthie Liang, Ariel Pollock Star, Nofar Tsur, Moshe Shmueli, Norm O'Rourke

Background: In contrast to all previous generations, life today is lived both in-person and online. This creates both opportunities and risks to mental health and well-being. Social interaction is no longer geographically constrained, yet the anonymity and impersonality of social media create new problems. To quote Mike Tyson (July 2020), "Social media have made y'all way too comfortable with disrespecting people and not getting punched in the face for it."

Objective: This study set out to propose and test a hypothesized model to identify both direct and indirect predictors of life satisfaction. Independent or predictor variables included social media use, loneliness, and online and traditional social support.

Methods: From March 2024 to October 2024, a total of 112 adults in the United States were recruited online and proceeded to complete study questionnaires. Participants were aged 42.62 (SD 12.74) years on average, had completed an average of 15.46 (SD 3.25) years of education, and reported an average household income of US $67,005 (SD US $41,560) per year.

Results: Using path analysis, we found that social media use and online social support emerged as significant, indirect predictors of life satisfaction via loneliness and traditional in-person social support (P<.01). In total, 39% of variance in life satisfaction was explained by this path model (R2=0.39; P<.01).

Conclusions: Contrary to hypothesis, these findings support the rich get richer hypothesis regarding online social support, not the social compensation theory, that is, online social support appears to function as an adjunct to in-person support, not as a substitute. The results of this study need to be replicated with more diverse, larger samples, with responses collected over multiple time points.

背景:与前几代人相比,今天的生活既包括面对面的生活,也包括在线生活。这既为精神健康和福祉创造了机会,也带来了风险。社交互动不再受地域限制,但社交媒体的匿名性和非人格化带来了新的问题。引用迈克·泰森(2020年7月)的话:“社交媒体让你们对不尊重别人感到太舒服了,而且不会因此被打脸。”目的:本研究提出并测试了一个假设模型,以确定生活满意度的直接和间接预测因素。独立变量或预测变量包括社交媒体使用、孤独感、在线和传统社会支持。方法:从2024年3月到2024年10月,在美国共招募了112名成年人,并开始完成研究问卷。参与者的平均年龄为42.62岁(标准差12.74),平均完成教育年限为15.46年(标准差3.25),平均家庭年收入为67,005美元(标准差41,560美元)。结果:通过通径分析,我们发现社交媒体使用和网络社会支持通过孤独和传统的面对面社会支持成为生活满意度的显著间接预测因子(P2=0.39; p)。结论:与假设相反,这些发现支持关于网络社会支持的“富人越富”假设,而不是社会补偿理论,即网络社会支持似乎是面对面支持的辅助,而不是替代。这项研究的结果需要用更多样化、更大的样本来重复,并在多个时间点收集反馈。
{"title":"Online Social Support - an Adjunct or Substitute for Traditional Social Support: Cross-Sectional Study.","authors":"Ruthie Liang, Ariel Pollock Star, Nofar Tsur, Moshe Shmueli, Norm O'Rourke","doi":"10.2196/90751","DOIUrl":"10.2196/90751","url":null,"abstract":"<p><strong>Background: </strong>In contrast to all previous generations, life today is lived both in-person and online. This creates both opportunities and risks to mental health and well-being. Social interaction is no longer geographically constrained, yet the anonymity and impersonality of social media create new problems. To quote Mike Tyson (July 2020), \"Social media have made y'all way too comfortable with disrespecting people and not getting punched in the face for it.\"</p><p><strong>Objective: </strong>This study set out to propose and test a hypothesized model to identify both direct and indirect predictors of life satisfaction. Independent or predictor variables included social media use, loneliness, and online and traditional social support.</p><p><strong>Methods: </strong>From March 2024 to October 2024, a total of 112 adults in the United States were recruited online and proceeded to complete study questionnaires. Participants were aged 42.62 (SD 12.74) years on average, had completed an average of 15.46 (SD 3.25) years of education, and reported an average household income of US $67,005 (SD US $41,560) per year.</p><p><strong>Results: </strong>Using path analysis, we found that social media use and online social support emerged as significant, indirect predictors of life satisfaction via loneliness and traditional in-person social support (P<.01). In total, 39% of variance in life satisfaction was explained by this path model (R<sup>2</sup>=0.39; P<.01).</p><p><strong>Conclusions: </strong>Contrary to hypothesis, these findings support the rich get richer hypothesis regarding online social support, not the social compensation theory, that is, online social support appears to function as an adjunct to in-person support, not as a substitute. The results of this study need to be replicated with more diverse, larger samples, with responses collected over multiple time points.</p>","PeriodicalId":14841,"journal":{"name":"JMIR Formative Research","volume":"10 ","pages":"e90751"},"PeriodicalIF":2.0,"publicationDate":"2026-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13003209/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147365261","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
Process Evaluation of Interdisciplinary Experiences During the Development of a Serious Game About Radiotherapy for Children: Qualitative Interview Study. 儿童放射治疗严肃游戏开发过程中跨学科经验的过程评价:质性访谈研究。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-03-05 DOI: 10.2196/71454
Catarina Cederved, Jon Back, Gustaf Ljungman, Charlotte Ångström Brännström, Gunn Engvall

Background: It is considered advantageous to adopt an interdisciplinary approach when creating serious games in the sphere of health practice. However, different fields have reported that interdisciplinary work is challenging. Yet, the literature is scarce regarding how participants within health research have experienced collaborative research. In 2019 and 2020, total 3 teams collaborated to produce a serious game for children undergoing radiotherapy.

Objective: The aim of this study was to describe the experiences of collaborating within and between teams, during their participation in the development of a serious game about radiotherapy for children.

Methods: A qualitative design was used for gathering data through in depth interviews and a reflective thematic analysis was made. The collaboration included 15 people, 14 of them were asked to participate and 13 accepted. The teams included a game design team, a research team, and an expert team. The latter consisted of a play therapist, a pediatric nurse, and radiation oncology nurses.

Results: In total, 1 main theme and 4 subthemes were formulated. The main theme was a learning experience during the participatory process. The subthemes were: (1) new insights were established due to the collaboration, (2) discovering the mechanisms behind the design elements provided understanding of the game's complexity, (3) collaboration within teams and between teams needs time and takes time, and (4) confidence that the project was going to make a difference created engagement.

Conclusions: In conclusion, knowledge expansion arose on several levels during the time the participants were part of the project. Having time and building trust in team constellations are significant factors in achieving a productive, favorable and beneficial experience for participants. Furthermore, confidence in the usefulness of the end product could be a contributory factor for participants continuing to work and the understanding of the complexity of the evolving process. Based on the findings of the team members' individual experiences, we recommend other medical research teams to consider the following implications for practice before starting interdisciplinary design research: (1) establish who can bridge the fields and act to establish mutual understanding; (2) make time for frequent meetings to update on progress; and (3) be responsive, because when everybody feels connected to what needs to be done and feel safe it gets easier to work together.

背景:在健康实践领域制作严肃游戏时,采用跨学科方法被认为是有利的。然而,不同的领域报告说,跨学科的工作是具有挑战性的。然而,关于健康研究参与者如何经历合作研究的文献很少。2019年和2020年,共有3个团队合作为接受放射治疗的儿童制作了一款严肃的游戏。目的:本研究的目的是描述团队内部和团队之间的合作经验,在他们参与开发一个关于儿童放射治疗的严肃游戏。方法:采用定性设计,通过深度访谈收集资料,并进行反思性专题分析。这项合作包括15人,其中14人被要求参与,13人被接受。这些团队包括一个游戏设计团队、一个研究团队和一个专家团队。后者由一名游戏治疗师、一名儿科护士和一名放射肿瘤学护士组成。结果:共制定1个主旋律和4个副旋律。主题是参与过程中的学习经验。子主题是:(1)由于合作而产生新的见解;(2)发现设计元素背后的机制,从而理解游戏的复杂性;(3)团队内部和团队之间的合作需要时间,也需要时间;(4)对项目将产生影响的信心创造粘性。结论:总之,在参与者参与项目期间,知识扩展出现在几个层面上。在团队中投入时间和建立信任是为参与者获得富有成效、有利和有益体验的重要因素。此外,对最终产品有用性的信心可能是促进参与者继续工作和了解演变过程的复杂性的一个因素。根据团队成员个人经验的发现,我们建议其他医学研究团队在开始跨学科设计研究之前考虑以下实践意义:(1)确定谁可以弥合领域并采取行动建立相互理解;(2)留出时间,经常召开会议,通报进展情况;(3)积极响应,因为当每个人都感到与需要做的事情有联系并感到安全时,就会更容易一起工作。
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引用次数: 0
Automated Annotation of Pain Chronicity in Patients With Back Pain by Using Electronic Health Records: Retrospective Study. 使用电子健康记录自动标注背痛患者的疼痛慢性性:回顾性研究。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-03-05 DOI: 10.2196/63198
Simran Ajay Kanal, Jeannie Bailey, Jeffrey Lotz, Aaron Scheffler, Thomas Peterson

Background: Chronic back pain is a severe health condition with underlying biopsychosocial factors that make diagnosis difficult, and pain chronicity has been shown to be an important variable for studying patient outcomes. Due to the absence of standardized criteria, pain chronicity needs to be manually annotated by clinicians in electronic health records (EHRs), which is not only time consuming but also has the potential to introduce variability in analysis and interpretation among practitioners.

Objective: Pain chronicity is not typically recorded in EHRs and currently needs to be manually annotated by experts. Using a dataset from an interdisciplinary spine clinic consisting of 386 patients manually annotated for pain chronicity by clinical experts, this study has two objectives: (1) to examine the relationship between expert-annotated chronicity and social determinant variables present in EHRs and (2) to evaluate the feasibility of extracting pain chronicity from the EHR without expert annotation.

Methods: We used a supervised machine learning model, specifically univariate regression, to examine associations between clinician-annotated pain chronicity values and the structured variables present in EHRs. Next, we trained a random forest model to predict pain chronicity by using both structured and unstructured data extracted by clinical Text Analysis and Knowledge Extraction System, a natural language processing (NLP) tool. The features extracted included clinical keywords; duration of pain reported; and the International Classification of Diseases, Tenth Revision codes. The model was assessed using the Pearson correlation coefficient and mean absolute error (MAE).

Results: The study analyzed 386 patients (mean age 60.2 years, SD 16.1 years and median age 62.0 years, IQR 48.8-72.0 years) from the San Francisco Bay Area, with 62.7% (n=242) identifying as women. Our univariate regression analysis identified structured EHR variables associated with pain chronicity, which include pain severity before the last visit (P=.006), number of imaging orders (P=.006), number of visits to the neurology department (P=.01), and Medi-Cal insurance coverage (P=.03). Our random forest model using structured data showed a strong correlation of 0.887 (P<.001) with an MAE of 18.45 between predicted and observed chronicity, whereas our model that used the NLP tool to extract information from unstructured clinical notes and structured data showed a slightly higher correlation of 0.968 (P<.001) with an MAE of 10.87 between predicted and observed chronicity.

Conclusions: Our study indicates that pain chronicity from EHR data could be used to study more topics on larger datasets in the future without the need for manual annotation and that using NLP tools to automate prediction is feasible.

背景:慢性背痛是一种严重的健康状况,其潜在的生物心理社会因素使诊断困难,疼痛的慢性性已被证明是研究患者预后的一个重要变量。由于缺乏标准化的标准,慢性疼痛需要由临床医生在电子健康记录(EHRs)中手工注释,这不仅耗时,而且有可能在从业者之间的分析和解释中引入差异。目的:疼痛慢性性通常不记录在电子病历中,目前需要由专家手工注释。本研究使用跨学科脊柱诊所的数据集,包括386名由临床专家手工注释的疼痛慢性性患者,本研究有两个目标:(1)检查专家注释的慢性性与电子病历中存在的社会决定变量之间的关系;(2)评估从没有专家注释的电子病历中提取疼痛慢性性的可行性。方法:我们使用有监督的机器学习模型,特别是单变量回归,来检查临床医生注释的疼痛慢性值与电子病历中存在的结构化变量之间的关系。接下来,我们利用临床文本分析和知识提取系统(一种自然语言处理工具)提取的结构化和非结构化数据,训练随机森林模型来预测疼痛的慢性性。提取的特征包括临床关键词;报告的疼痛持续时间;以及国际疾病分类第十次修订代码。采用Pearson相关系数和平均绝对误差(MAE)对模型进行评估。结果:研究分析了旧金山湾区386例患者(平均年龄60.2岁,SD 16.1岁,中位年龄62.0岁,IQR 48.8-72.0岁),其中62.7% (n=242)为女性。我们的单变量回归分析确定了与疼痛慢性相关的结构化电子病历变量,包括上次就诊前的疼痛严重程度(P= 0.006)、影像学检查次数(P= 0.006)、神经科就诊次数(P= 0.01)和Medi-Cal保险覆盖率(P= 0.03)。结论:我们的研究表明,来自电子病历数据的疼痛慢性性可以在未来更大的数据集上用于研究更多的主题,而不需要人工注释,使用NLP工具自动预测是可行的。
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引用次数: 0
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