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Multimodal Transformer-Based Electrocardiogram Analysis for Cardiovascular Comorbidity Detection: Model Development and Validation Study. 基于多模态变压器的心血管共病检测心电图分析:模型开发与验证研究。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-01-02 DOI: 10.2196/80815
Zi Yang, Xiaojuan Wang, Jianlin Wang, Qi Guang, Xueqian Ding, Hao Liu, Yunpeng Xu, Jing Zhao, Ming Bai

Background: Cardiovascular diseases remain the leading global cause of mortality, yet traditional electrocardiogram (ECG) interpretation shows subjective variability and limited sensitivity to complex pathologies.

Objective: This study aims to address these challenges by proposing the Cardiovascular Multimodal Prediction Network (CaMPNet), a transformer-based multimodal architecture that integrates raw 12-lead ECG waveforms, 9-structured machine-measured ECG features, and demographic data (age and sex) through cross-attention fusion.

Methods: The model was trained on 384,877 records from the Medical Information Mart for Intensive Care IV - Electrocardiogram Matched Subset database and evaluated across 12 cardiovascular disease labels. To further assess temporal robustness, a temporal external validation was performed using the most recent 10% of the data, withheld chronologically from model development.

Results: On the internal test set, the model achieved a mean area under the curve (AUC) of 0.845 (SD 0.04) and area under the precision-recall curve of 0.489, outperforming the residual networks-ECG baseline (AUC=0.848 but F1-score=0.152) and all single-modality variants. Subgroup analyses demonstrated consistent performance across demographics (male AUC= 0.846 vs female=0.843; youngest quartile 0.884 vs oldest 0.811). CaMPNet retained moderate discriminative ability in temporal external validation with a mean AUC of 0.715 (SD 0.03) and area under the precision-recall curve of 0.298, although performance declined due to temporal distribution shifts. Despite this, major disease categories, such as atrial fibrillation, heart failure, and normal rhythm, maintained high AUCs (>0.84). Attention-based visualization revealed clinically interpretable patterns (eg, ST-segment elevations in ST-segment elevation myocardial infarction), and ablation experiments verified the model's tolerance to missing structured inputs.

Conclusions: CaMPNet demonstrates robust and interpretable multimodal ECG-based diagnosis, offering a scalable framework for comorbidity screening and continual learning under real-world temporal dynamics.

背景:心血管疾病仍然是全球死亡的主要原因,但传统的心电图(ECG)解释显示主观变异性和对复杂病理的有限敏感性。目的:本研究旨在通过提出心血管多模态预测网络(CaMPNet)来解决这些挑战,这是一种基于变压器的多模态架构,通过交叉注意融合集成了原始的12导联ECG波形、9结构化机器测量的ECG特征和人口统计数据(年龄和性别)。方法:该模型在重症监护医学信息市场-心电图匹配子集数据库中的384,877条记录上进行训练,并在12种心血管疾病标签上进行评估。为了进一步评估时间稳健性,使用最近10%的数据进行时间外部验证,按时间顺序从模型开发中保留。结果:在内部测试集上,该模型的平均曲线下面积(AUC)为0.845 (SD 0.04),精确召回率曲线下面积为0.489,优于残差网络- ecg基线(AUC=0.848, F1-score=0.152)和所有单模态变量。亚组分析显示了不同人口统计数据的一致表现(男性AUC= 0.846 vs女性=0.843;最年轻四分位数0.884 vs最年长的0.811)。CaMPNet在时间外部验证中保持了中等的判别能力,平均AUC为0.715 (SD为0.03),精确召回率曲线下面积为0.298,但性能因时间分布的变化而下降。尽管如此,主要疾病类别,如心房颤动、心力衰竭和正常心律,仍保持较高的auc(>0.84)。基于注意力的可视化显示了临床可解释的模式(例如,st段抬高型心肌梗死的st段抬高),消融实验验证了该模型对缺失结构化输入的耐受性。结论:CaMPNet展示了稳健且可解释的基于多模态心电图的诊断,为合并症筛查和现实世界时间动态下的持续学习提供了可扩展的框架。
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引用次数: 0
Characterization of Post-Viral Infection Behaviors Among Patients With Long COVID: Prospective, Observational, Longitudinal Cohort Analyses of Fitbit Data and Patient-Reported Outcomes. 长冠肺炎患者病毒感染后行为特征:Fitbit数据和患者报告结果的前瞻性、观察性、纵向队列分析
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-12-31 DOI: 10.2196/77644
Tianmai M Zhang, Sydney P Sharp, John D Scott, Douglas Taren, Jane C Samaniego, Elizabeth R Unger, Jeanne Bertolli, Jin-Mann S Lin, Christian B Ramers, Job G Godino
<p><strong>Background: </strong>Long COVID encompasses a range of health problems that can be highly debilitating. While some research has relied on self-reported measures of symptoms and functioning, few studies have characterized symptoms in relation to behaviors and physiology measured objectively through wearable devices.</p><p><strong>Objective: </strong>The primary aim of this study was to identify longitudinal patterns in physical activity, physiology, and patient-reported outcomes (PROs) among patients with long COVID at a Federally Qualified Health Center in the United States. The secondary aim was to identify meaningful subgroups or phenotypes within this cohort and examine how PROs and symptoms overlay with physical activity characteristics.</p><p><strong>Methods: </strong>This was a prospective, observational, longitudinal cohort study recruiting a subset of low-income patients enrolled in the Long COVID and Fatiguing Illness Recovery Program. From March 2022 to May 2023, a total of 172 patients with long COVID or myalgic encephalomyelitis/chronic fatigue syndrome were given Fitbit Charge 5 (Fitbit Inc) devices and instructed to wear them continuously for up to a year. Patients completed PRO questionnaires (PROMIS-29 [Patient-Reported Outcomes Measurement Information System-29] and symptom questionnaires, etc) at baseline, 3, and 6 months. Inclusion in longitudinal analysis required at least 20 hours of valid wear data per day for a minimum of 7 days. The World Health Organization guideline on moderate to vigorous physical activity (MVPA) was used to differentiate MPVA-active and MVPA-inactive patients. Linear mixed effects regression was performed to assess longitudinal associations between physical activity levels and PROs.</p><p><strong>Results: </strong>Among 172 patients, 80.2% (n=138) were female, 75.6% (n=130) were White, 45.3% (n=78) were unemployed, and 94.8% (n=163) had estimated annual income below US $50,000. Of these patients, 82 (47.7%) met valid wear criteria, providing 50.5 days of Fitbit data on average. At baseline, MVPA-inactive patients (n=41) reported statistically more severe problems regarding physical function, fatigue, and dyspnea than MVPA-active patients (n=41) on both continuous and categorical scales, with P<.05 from both Student t tests (2-tailed) and chi-squared tests. Longitudinal analysis found that MVPA-inactive patients showed a decreased ability to participate in social roles (estimated group difference=-4.21 T-score points over 3 months, 95% CI -6.64 to -1.78, P<.001) and a higher intensity of sleep symptoms (estimated group difference=2.06 severity score points over 3 months, 95% CI 0.40 to 3.71, P=.02) over time.</p><p><strong>Conclusions: </strong>This study showed that patients with long COVID could remain MVPA-active despite experiencing symptoms. These findings provide insights into the relationship between PROs, physical activity, and long COVID, which suggests the importance of considering
背景:长冠状病毒病包括一系列可能非常令人虚弱的健康问题。虽然一些研究依赖于自我报告的症状和功能测量,但很少有研究通过可穿戴设备客观测量与行为和生理相关的症状。目的:本研究的主要目的是确定美国联邦合格医疗中心长COVID患者的身体活动、生理和患者报告结果(PROs)的纵向模式。次要目的是在该队列中确定有意义的亚组或表型,并检查PROs和症状如何与身体活动特征重叠。方法:这是一项前瞻性、观察性、纵向队列研究,招募了一组参加长期COVID和疲劳性疾病康复计划的低收入患者。从2022年3月至2023年5月,共有172名患有长冠状病毒或肌痛性脑脊髓炎/慢性疲劳综合征的患者使用Fitbit Charge 5 (Fitbit Inc .)设备,并指导他们连续佩戴长达一年。患者分别在基线、3、6个月完成PRO问卷(promise -29[患者报告结果测量信息系统-29]和症状问卷等)。纳入纵向分析需要每天至少20小时的有效磨损数据,持续至少7天。采用世界卫生组织关于中度至剧烈体育活动(MVPA)的指南来区分mpva活跃和MVPA不活跃的患者。采用线性混合效应回归来评估体力活动水平与PROs之间的纵向关联。结果:172例患者中,80.2% (n=138)为女性,75.6% (n=130)为白人,45.3% (n=78)为无业人员,94.8% (n=163)年收入低于5万美元。在这些患者中,82例(47.7%)符合有效磨损标准,平均提供50.5天的Fitbit数据。在基线时,在连续和分类量表上,mvpa不活跃患者(n=41)报告的身体功能、疲劳和呼吸困难问题在统计上比mvpa活跃患者(n=41)更严重。结论:本研究表明,长COVID患者尽管出现症状,但仍可以保持mvpa活跃。这些发现为pro、身体活动和长COVID之间的关系提供了见解,这表明在制定治疗计划时考虑个人活动概况的重要性,特别是在低收入人群中。考虑到其探索性和局限性,包括高流失率和缺失数据,本研究的发现应被解释为假设生成。
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引用次数: 0
Health Care Utilization in Patients With Atopic Dermatitis Experiencing Topical Steroid Withdrawal: Observational Cross-Sectional Social Media Questionnaire Study. 特应性皮炎患者的医疗保健利用经历局部类固醇戒断:观察性横断面社会媒体问卷研究
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-12-31 DOI: 10.2196/85183
Alexander Shayesteh, Maja Af Klinteberg, Sophie Vrang, Gunnthorunn Sigurdardottir, MariHelen Sandström Falk, Mikael Alsterholm
<p><strong>Background: </strong>Topical steroid withdrawal (TSW) is a controversial skin condition among health care providers due to a lack of evidence, but it has an impactful and growing presence on social media. There are few previous reports of health care utilization for symptoms attributed to TSW.</p><p><strong>Objective: </strong>This study aims to investigate health care utilization and requests as well as information sources for TSW among patients with atopic dermatitis (AD).</p><p><strong>Methods: </strong>This observational cross-sectional study used a questionnaire aimed at adults with AD, experiencing symptoms they attribute to TSW. The questionnaire was posted as a link, free to share with others, in a Swedish TSW-themed Facebook group and remained accessible for 4 weeks. Descriptive statistics and topical text analysis on open-ended items were used to present and interpret the results.</p><p><strong>Results: </strong>The participants (n=82) reported dermatologists (n=41, 50%), general practitioners (n=40, 49%), and practitioners of complementary and alternative medicine (CAM; n=32, 39%) as the most frequent health care contacts for TSW. However, among participants with ongoing symptoms attributed to TSW (n=68), ongoing health care contacts with general practitioners, dermatologists, and practitioners of CAM were reported by only 10% (n=7), 22% (n=15), and 13% (n=11), respectively. For symptoms attributed to AD, the frequencies of health care provider contacts were higher. Almost all participants had sought help from a general practitioner (n=81, 99%) or a dermatologist (n=76, 93%) at some point, and many had also consulted a practitioner of CAM (n=59, 72%). Among those with ongoing symptoms attributed to AD, 43% (n=26) had an ongoing contact with a dermatologist. Participant-requested help and support from health care providers included understanding and confirmation of TSW impairments (n=45, 56%), treatment of symptoms (n=26, 32%), and increased awareness and information about TSW from health care providers (n=21, 26%). The most common TSW information sources were Facebook (n=78, 96%), websites (n=75, 93%), and Instagram (n=45, 56%), but YouTube (n=11, 14%), podcasts (n=7, 10%), and TikTok (n=5, 6%) were also reported.</p><p><strong>Conclusions: </strong>This study investigates health care utilization patterns related to TSW. The results indicate that the participants received insufficient support from health care providers for symptoms they attributed to TSW. The participants initiated and maintained health care provider contacts for symptoms attributed to AD to a greater extent than for TSW and sought information and support for TSW elsewhere. Targeted interventions to overcome this could be educational efforts for general practitioners and dermatologists about the current scientific knowledge of TSW as well as the TSW discourse on social media. In addition, health care providers need to engage and contribute to evidence-based
背景:由于缺乏证据,局部类固醇戒断(TSW)在医疗保健提供者中是一种有争议的皮肤病,但它在社交媒体上的影响力越来越大。以前很少有关于TSW症状的医疗保健利用的报道。目的:了解特应性皮炎(AD)患者对TSW的医疗保健利用、需求及信息来源。方法:这项观察性横断面研究使用了一份问卷,针对患有AD的成人,他们认为这些症状是TSW引起的。调查问卷以链接的形式发布在瑞典tsw主题的Facebook群中,可以免费与他人分享,并在四周内保持可访问性。使用描述性统计和开放式项目的主题文本分析来呈现和解释结果。结果:参与者(n=82)报告皮肤科医生(n= 41,50%),全科医生(n= 40,49%)和补充和替代医学医生(n= 32,39%)是TSW最常见的医疗保健接触者。然而,在持续出现TSW症状的参与者(n=68)中,分别报告与全科医生、皮肤科医生和CAM医生进行卫生保健接触的人数分别为10% (n=7)、22% (n=15)和13% (n=11)。对于归因于AD的症状,与卫生保健提供者接触的频率更高。几乎所有的参与者都曾向全科医生(n= 81,99%)或皮肤科医生(n= 76,93%)寻求过帮助,许多人还咨询过CAM的医生(n= 59,72%)。在持续出现AD症状的患者中,43% (n=26)与皮肤科医生有持续接触。参与者要求卫生保健提供者提供的帮助和支持包括了解和确认TSW损伤(n=45, 56%),治疗症状(n=26, 32%),以及提高卫生保健提供者对TSW的认识和信息(n=21, 26%)。最常见的TSW信息源是Facebook (n= 78,96%)、网站(n= 75,93%)和Instagram (n= 45,56%),但YouTube (n= 11,14%)、播客(n= 7,10%)和TikTok (n= 5,6%)也有报道。结论:本研究探讨与身心健康相关的医疗保健利用模式。结果表明,参与者没有得到足够的支持,从卫生保健提供者的症状,他们归咎于TSW。与TSW相比,由于AD引起的症状,参与者开始并保持与医疗保健提供者的联系,并在其他地方寻求TSW的信息和支持。有针对性的干预措施可以克服这一点,对全科医生和皮肤科医生进行有关TSW当前科学知识以及社交媒体上TSW话语的教育努力。此外,卫生保健提供者需要在相关的社交媒体平台上参与并促进有关TSW的循证内容,以防止有关局部糖皮质激素的错误信息传播。
{"title":"Health Care Utilization in Patients With Atopic Dermatitis Experiencing Topical Steroid Withdrawal: Observational Cross-Sectional Social Media Questionnaire Study.","authors":"Alexander Shayesteh, Maja Af Klinteberg, Sophie Vrang, Gunnthorunn Sigurdardottir, MariHelen Sandström Falk, Mikael Alsterholm","doi":"10.2196/85183","DOIUrl":"10.2196/85183","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;Topical steroid withdrawal (TSW) is a controversial skin condition among health care providers due to a lack of evidence, but it has an impactful and growing presence on social media. There are few previous reports of health care utilization for symptoms attributed to TSW.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;This study aims to investigate health care utilization and requests as well as information sources for TSW among patients with atopic dermatitis (AD).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;This observational cross-sectional study used a questionnaire aimed at adults with AD, experiencing symptoms they attribute to TSW. The questionnaire was posted as a link, free to share with others, in a Swedish TSW-themed Facebook group and remained accessible for 4 weeks. Descriptive statistics and topical text analysis on open-ended items were used to present and interpret the results.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;The participants (n=82) reported dermatologists (n=41, 50%), general practitioners (n=40, 49%), and practitioners of complementary and alternative medicine (CAM; n=32, 39%) as the most frequent health care contacts for TSW. However, among participants with ongoing symptoms attributed to TSW (n=68), ongoing health care contacts with general practitioners, dermatologists, and practitioners of CAM were reported by only 10% (n=7), 22% (n=15), and 13% (n=11), respectively. For symptoms attributed to AD, the frequencies of health care provider contacts were higher. Almost all participants had sought help from a general practitioner (n=81, 99%) or a dermatologist (n=76, 93%) at some point, and many had also consulted a practitioner of CAM (n=59, 72%). Among those with ongoing symptoms attributed to AD, 43% (n=26) had an ongoing contact with a dermatologist. Participant-requested help and support from health care providers included understanding and confirmation of TSW impairments (n=45, 56%), treatment of symptoms (n=26, 32%), and increased awareness and information about TSW from health care providers (n=21, 26%). The most common TSW information sources were Facebook (n=78, 96%), websites (n=75, 93%), and Instagram (n=45, 56%), but YouTube (n=11, 14%), podcasts (n=7, 10%), and TikTok (n=5, 6%) were also reported.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;This study investigates health care utilization patterns related to TSW. The results indicate that the participants received insufficient support from health care providers for symptoms they attributed to TSW. The participants initiated and maintained health care provider contacts for symptoms attributed to AD to a greater extent than for TSW and sought information and support for TSW elsewhere. Targeted interventions to overcome this could be educational efforts for general practitioners and dermatologists about the current scientific knowledge of TSW as well as the TSW discourse on social media. In addition, health care providers need to engage and contribute to evidence-based ","PeriodicalId":14841,"journal":{"name":"JMIR Formative Research","volume":"9 ","pages":"e85183"},"PeriodicalIF":2.0,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12755344/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145878339","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
Impact of Cross-Sectoral Video Consultation on Perceived Care Coordination and Information Satisfaction in Cancer Care: Randomized Controlled Trial. 跨部门视像会诊对癌症照护认知协调及资讯满意度的影响:随机对照试验。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-12-31 DOI: 10.2196/76910
Fereshteh Baygi, Theis Bitz Trabjerg, Lars Henrik Jensen, Maria Munch Storsveen, Sonja Wehberg, Jens Søndergaard, Dorte Gilså Hansen

Background: Enhancing care coordination and sharing information in cancer care improves patient experiences by promoting clarity and satisfaction.

Objective: This study aims to assess the impact of cross-sectoral video consultation on patient perceptions of care coordination and satisfaction with received information compared to usual care.

Methods: This study presents secondary outcomes on patient perceptions of care coordination and satisfaction with received information from a 7-month follow-up of the Partnership Project. In this randomized controlled trial, patients with cancer were allocated to either an intervention group receiving cross-sectoral video consultation (oncologist, general practitioner, and patient) or a control group receiving usual care. Patients' perceptions of care coordination and information quality were assessed using the Australian Cancer Care Coordination Questionnaire (CCCQ) and the European Organisation for Research and Treatment of Cancer Quality of Life Information Questionnaire 25 at baseline and 7 months. Changes over time between groups were analyzed using generalized estimating equations.

Results: Of the 278 participants randomized (1:1), only 80 (28.8%) patients received the intervention due to technical and administrative issues. A total of 210 (75.5%) patients completed the baseline questionnaire, while 118 (42.4%) responded at 7 months. No significant differences were observed in the changes over time between the intervention and control groups in any outcome. The estimated differences in the change in score from baseline to 7 months were as follows: for the total CCCQ score, 1.11 (95% CI -2.32 to 4.53; P=.53); for the overall European Organisation for Research and Treatment of Cancer Quality of Life Information Questionnaire 25 score, 1.49 (95% CI -2.98 to 5.96; P=.51); for the CCCQ communication subscale, -1.49 (95% CI -1.33 to 4.31; P=.30); and for the navigation subscale, -0.03 (95% CI -1.52 to 1.46; P=.97).

Conclusions: Our findings indicate no statistically significant improvement in patients' reported care coordination or satisfaction with received information over 7 months. Technical issues with the video setup reduced fidelity rates and follow-up participation. Further research is needed to optimize the structure and content of cross-sectoral video consultations to better support patients' perceived outcomes.

Trial registration: ClinicalTrials.gov NCT02716168; https://clinicaltrials.gov/study/NCT02716168.

背景:在癌症治疗中加强护理协调和信息共享,通过提高清晰度和满意度来改善患者体验。目的:本研究旨在评估与常规护理相比,跨部门视频会诊对患者对护理协调和接收信息满意度的影响。方法:本研究从7个月的伙伴关系项目随访中获得患者对护理协调的感知和对接收信息的满意度的次要结果。在这项随机对照试验中,癌症患者被分配到接受跨部门视频咨询的干预组(肿瘤科医生、全科医生和患者)或接受常规护理的对照组。在基线和7个月时,使用澳大利亚癌症护理协调问卷(CCCQ)和欧洲癌症研究和治疗组织生活质量信息问卷25来评估患者对护理协调和信息质量的看法。使用广义估计方程分析各组间随时间的变化。结果:在278名随机(1:1)参与者中,由于技术和管理问题,只有80名(28.8%)患者接受了干预。共有210名(75.5%)患者完成了基线问卷,118名(42.4%)患者在7个月时回复了问卷。在任何结果上,干预组和对照组之间没有观察到随时间变化的显著差异。从基线到7个月评分变化的估计差异如下:CCCQ总评分为1.11 (95% CI -2.32 ~ 4.53; P= 0.53);欧洲癌症研究与治疗组织总体生活质量信息问卷25分,1.49 (95% CI -2.98 ~ 5.96; P= 0.51);CCCQ通信子量表为-1.49 (95% CI为-1.33 ~ 4.31;P= 0.30);导航子量表为-0.03 (95% CI为-1.52至1.46;P= 0.97)。结论:我们的研究结果表明,在7个月的时间里,患者报告的护理协调或对收到的信息的满意度没有统计学上的显著改善。视频设置的技术问题降低了保真率和后续参与。需要进一步研究优化跨部门视频会诊的结构和内容,以更好地支持患者的感知结果。试验注册:ClinicalTrials.gov NCT02716168;https://clinicaltrials.gov/study/NCT02716168。
{"title":"Impact of Cross-Sectoral Video Consultation on Perceived Care Coordination and Information Satisfaction in Cancer Care: Randomized Controlled Trial.","authors":"Fereshteh Baygi, Theis Bitz Trabjerg, Lars Henrik Jensen, Maria Munch Storsveen, Sonja Wehberg, Jens Søndergaard, Dorte Gilså Hansen","doi":"10.2196/76910","DOIUrl":"https://doi.org/10.2196/76910","url":null,"abstract":"<p><strong>Background: </strong>Enhancing care coordination and sharing information in cancer care improves patient experiences by promoting clarity and satisfaction.</p><p><strong>Objective: </strong>This study aims to assess the impact of cross-sectoral video consultation on patient perceptions of care coordination and satisfaction with received information compared to usual care.</p><p><strong>Methods: </strong>This study presents secondary outcomes on patient perceptions of care coordination and satisfaction with received information from a 7-month follow-up of the Partnership Project. In this randomized controlled trial, patients with cancer were allocated to either an intervention group receiving cross-sectoral video consultation (oncologist, general practitioner, and patient) or a control group receiving usual care. Patients' perceptions of care coordination and information quality were assessed using the Australian Cancer Care Coordination Questionnaire (CCCQ) and the European Organisation for Research and Treatment of Cancer Quality of Life Information Questionnaire 25 at baseline and 7 months. Changes over time between groups were analyzed using generalized estimating equations.</p><p><strong>Results: </strong>Of the 278 participants randomized (1:1), only 80 (28.8%) patients received the intervention due to technical and administrative issues. A total of 210 (75.5%) patients completed the baseline questionnaire, while 118 (42.4%) responded at 7 months. No significant differences were observed in the changes over time between the intervention and control groups in any outcome. The estimated differences in the change in score from baseline to 7 months were as follows: for the total CCCQ score, 1.11 (95% CI -2.32 to 4.53; P=.53); for the overall European Organisation for Research and Treatment of Cancer Quality of Life Information Questionnaire 25 score, 1.49 (95% CI -2.98 to 5.96; P=.51); for the CCCQ communication subscale, -1.49 (95% CI -1.33 to 4.31; P=.30); and for the navigation subscale, -0.03 (95% CI -1.52 to 1.46; P=.97).</p><p><strong>Conclusions: </strong>Our findings indicate no statistically significant improvement in patients' reported care coordination or satisfaction with received information over 7 months. Technical issues with the video setup reduced fidelity rates and follow-up participation. Further research is needed to optimize the structure and content of cross-sectoral video consultations to better support patients' perceived outcomes.</p><p><strong>Trial registration: </strong>ClinicalTrials.gov NCT02716168; https://clinicaltrials.gov/study/NCT02716168.</p>","PeriodicalId":14841,"journal":{"name":"JMIR Formative Research","volume":"9 ","pages":"e76910"},"PeriodicalIF":2.0,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145878327","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Ghana Heart Initiative Training for Cardiac Arrest Management Among Health Care Professionals: Outcomes Evaluation Study (2019-2024). 加纳心脏倡议培训在卫生保健专业人员心脏骤停管理:结果评估研究(2019-2024)。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-12-31 DOI: 10.2196/75536
Alfred Doku, Lawrence Sena Tuglo, Chiedozie Osuoji, Juliette Edzeame, Marisa Broni, David Danso Mainoo, Alberta Ewuziwaa Acquah, Kwatetso Honny, Ron J G Peters, Charles Agyemang

Background: Health care professionals must stay updated with the latest guidelines for basic life support (BLS) and advanced cardiac life support (ACLS) to effectively assist patients during cardiac emergencies. Since its launch in 2018, the Ghana Heart Initiative has significantly enhanced the skills and knowledge of health care professionals in managing cardiovascular diseases, including cardiac emergencies.

Objective: This study aims to assess the knowledge and skills of BLS and ACLS among health care professionals immediately after training in Ghana.

Methods: This cross-sectional, training-based study involved 541 and 302 health care professionals trained in BLS and ACLS, respectively. Among them, 229 BLS and 124 ACLS-trained participants completed the questionnaires immediately after the training, and their data were included in the final analysis. Knowledge was assessed using a standardized questionnaire and an instructor-led skills evaluation based on the updated 2018 and 2020 American Heart Association guidelines for cardiopulmonary resuscitation and emergency cardiovascular care.

Results: This study shows that 74.6% (171/229) of the health care professionals had adequate knowledge and skills in BLS. Those working in tertiary health care facilities were 80% less likely (adjusted odds ratio [AOR] 0.20, 95% CI 0.07-0.59; P=.003) to have adequate BLS knowledge and skills than those in primary health care facilities. Health care professionals from regions such as Volta and Oti were 4.94 times more likely to have adequate BLS knowledge and skills compared to those from Bono East (AOR 4.94, 95% CI 1.17-20.80; P=.03). Over 73.3% (91/124) of health care professionals had adequate knowledge and skills in ACLS. Males were 7.05 times more likely (AOR 7.05, 95% CI 2.69-18.46; P<.001) than females to possess adequate ACLS knowledge and skills.

Conclusions: Given an opportunity to learn and practice, health care professionals in Ghana attain adequate knowledge and skills in BLS and ACLS.

背景:医疗保健专业人员必须及时更新基本生命支持(BLS)和高级心脏生命支持(ACLS)的最新指南,以有效地帮助心脏紧急情况下的患者。自2018年启动以来,加纳心脏倡议大大提高了卫生保健专业人员在管理心血管疾病(包括心脏紧急情况)方面的技能和知识。目的:本研究旨在评估加纳卫生保健专业人员在培训后立即使用BLS和ACLS的知识和技能。方法:这项以培训为基础的横断面研究分别涉及541名和302名接受过BLS和ACLS培训的卫生保健专业人员。其中,经BLS培训的229名和经acls培训的124名参与者在培训结束后立即完成了问卷调查,其数据纳入最终分析。根据更新的2018年和2020年美国心脏协会心肺复苏和紧急心血管护理指南,使用标准化问卷和讲师指导的技能评估来评估知识。结果:74.6%(171/229)的卫生保健专业人员具备足够的BLS知识和技能。在三级卫生保健机构工作的人员比在初级卫生保健机构工作的人员掌握足够的劳工统计局知识和技能的可能性低80%(调整后的优势比[AOR] 0.20, 95% CI 0.07-0.59; P= 0.003)。来自Volta和Oti等地区的卫生保健专业人员拥有足够的BLS知识和技能的可能性是Bono East地区的4.94倍(AOR 4.94, 95% CI 1.17-20.80; P= 0.03)。超过73.3%(91/124)的医护人员具备足够的ACLS知识和技能。男性的可能性是7.05倍(AOR 7.05, 95% CI 2.69-18.46);结论:如果有机会学习和实践,加纳的卫生保健专业人员在BLS和ACLS方面获得了足够的知识和技能。
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引用次数: 0
Reach, Engagement, and Acceptability of a Subclinical Telehealth Service for Spanish-Speaking Adults: Retrospective Mixed Methods Pilot Study. 西班牙语成人亚临床远程医疗服务的覆盖面、参与度和可接受性:回顾性混合方法试点研究。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-12-31 DOI: 10.2196/80026
Marvyn R Arévalo Avalos, Julio Fu, Adrian Aguilera, Luis Suarez

Background: There is a gap in mental health care among Latino/x and Spanish-speaking communities, and the care that is available is often difficult to access, lacks cultural nuance, and results in low engagement and satisfaction.

Objective: The study aimed to evaluate the reach, adoption, and acceptability of digital Spanish-language psychosocial and emotional wellness services among Latino/x adults offered by the digital health company Sanarai.

Methods: Data included in this study were collected between August 2020 and September 2024 by Sanarai as part of its ongoing services. Quantitative data sources included individual customers' appointment data, individual session payment data, and customer satisfaction data. Qualitative data were obtained from transcribed notes of telephone or video-based user interviews conducted by Sanarai staff between August 2020 and May 2024.

Results: Between August 2020 and September 2024, Sanarai served 6163 users (n=3662, 59.42% women participants) across all 50 US states, with the highest concentration of participants in Texas and California. Results showed 94% (n=5793) of users scheduled a first appointment within 1 week, with 43% (n=2650) doing so within 1 day. Over 62.60% (n=3858) of participants engaged in two or more sessions, attending an average of 8.94 (SD 13) sessions over 110 days (SD 169). The platform delivered a total of 36,858 appointments, including individual and couples sessions. Only 22.47% (n=1385) of users responded to a customer satisfaction survey for a total of 2287 distinct responses; among this subgroup, session satisfaction was high with an average satisfaction rating of 4.88 out of 5.0 (SD 0.49) and a Net Promoter Score of +85. Nearly all responses (n=2174, 95.06%) expressed intent to schedule another session, but these results should be interpreted with caution, given the low response rate. Qualitative interviews with 30 users (n=21, 70% women) revealed a diverse user base. Many users reported prior mental health service experiences, while one-third were new to care. Participants cited cost, cultural fit, language access, and convenience as key reasons for choosing Sanarai over local services. Users highlighted the platform's affordability, scheduling flexibility, and provider professionalism as central to their positive experiences.

Conclusions: These findings underscore the value of culturally responsive, accessible online mental health care for Spanish-speaking communities.

背景:拉丁裔/x和西班牙语社区在精神卫生保健方面存在差距,现有的护理往往难以获得,缺乏文化差异,导致参与度和满意度低。目的:本研究旨在评估数字健康公司Sanarai提供的拉丁裔/x成人数字西班牙语社会心理和情感健康服务的覆盖范围、采用情况和可接受性。方法:纳入本研究的数据由Sanarai在2020年8月至2024年9月期间收集,作为其持续服务的一部分。定量数据源包括个人客户预约数据、个人会话支付数据和客户满意度数据。定性数据来自Sanarai工作人员在2020年8月至2024年5月期间进行的电话或视频用户访谈的转录记录。结果:在2020年8月至2024年9月期间,Sanarai在美国50个州服务了6163名用户(n=3662,女性参与者占59.42%),其中德克萨斯州和加利福尼亚州的参与者最为集中。结果显示,94% (n=5793)的用户在1周内安排了首次预约,43% (n=2650)的用户在1天内安排了首次预约。超过62.60% (n=3858)的参与者参加了两次或两次以上的会议,在110天内平均参加了8.94次(SD 13)会议(SD 169)。该平台共提供了36,858次预约,包括个人和夫妻会议。在2287个不同的回复中,只有22.47% (n=1385)的用户回应了客户满意度调查;在这个亚组中,会话满意度很高,平均满意度为4.88分(满分5.0分)(标准差0.49),净推荐值为+85。几乎所有的应答(n=2174, 95.06%)都表示打算安排另一个会话,但考虑到低应答率,这些结果应该谨慎解释。对30名用户(n= 21,70%为女性)的定性访谈揭示了多样化的用户基础。许多用户报告了以前的心理健康服务经历,而三分之一的人是第一次接受治疗。参与者认为,成本、文化契合度、语言获取和便利性是选择Sanarai而不是当地服务的主要原因。用户强调该平台的可负担性、调度灵活性和提供商的专业性是他们积极体验的核心。结论:这些发现强调了西班牙语社区文化响应性、可访问的在线精神卫生保健的价值。
{"title":"Reach, Engagement, and Acceptability of a Subclinical Telehealth Service for Spanish-Speaking Adults: Retrospective Mixed Methods Pilot Study.","authors":"Marvyn R Arévalo Avalos, Julio Fu, Adrian Aguilera, Luis Suarez","doi":"10.2196/80026","DOIUrl":"10.2196/80026","url":null,"abstract":"<p><strong>Background: </strong>There is a gap in mental health care among Latino/x and Spanish-speaking communities, and the care that is available is often difficult to access, lacks cultural nuance, and results in low engagement and satisfaction.</p><p><strong>Objective: </strong>The study aimed to evaluate the reach, adoption, and acceptability of digital Spanish-language psychosocial and emotional wellness services among Latino/x adults offered by the digital health company Sanarai.</p><p><strong>Methods: </strong>Data included in this study were collected between August 2020 and September 2024 by Sanarai as part of its ongoing services. Quantitative data sources included individual customers' appointment data, individual session payment data, and customer satisfaction data. Qualitative data were obtained from transcribed notes of telephone or video-based user interviews conducted by Sanarai staff between August 2020 and May 2024.</p><p><strong>Results: </strong>Between August 2020 and September 2024, Sanarai served 6163 users (n=3662, 59.42% women participants) across all 50 US states, with the highest concentration of participants in Texas and California. Results showed 94% (n=5793) of users scheduled a first appointment within 1 week, with 43% (n=2650) doing so within 1 day. Over 62.60% (n=3858) of participants engaged in two or more sessions, attending an average of 8.94 (SD 13) sessions over 110 days (SD 169). The platform delivered a total of 36,858 appointments, including individual and couples sessions. Only 22.47% (n=1385) of users responded to a customer satisfaction survey for a total of 2287 distinct responses; among this subgroup, session satisfaction was high with an average satisfaction rating of 4.88 out of 5.0 (SD 0.49) and a Net Promoter Score of +85. Nearly all responses (n=2174, 95.06%) expressed intent to schedule another session, but these results should be interpreted with caution, given the low response rate. Qualitative interviews with 30 users (n=21, 70% women) revealed a diverse user base. Many users reported prior mental health service experiences, while one-third were new to care. Participants cited cost, cultural fit, language access, and convenience as key reasons for choosing Sanarai over local services. Users highlighted the platform's affordability, scheduling flexibility, and provider professionalism as central to their positive experiences.</p><p><strong>Conclusions: </strong>These findings underscore the value of culturally responsive, accessible online mental health care for Spanish-speaking communities.</p>","PeriodicalId":14841,"journal":{"name":"JMIR Formative Research","volume":"9 ","pages":"e80026"},"PeriodicalIF":2.0,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12755293/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145878404","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
Prescribing Experiences, Potentials, and Challenges of Digital Health Applications in the Field of Hormones and Metabolism: Cross-Sectional Survey Study of Health Care Providers in Germany. 激素和代谢领域数字健康应用的处方经验、潜力和挑战:德国卫生保健提供者的横断面调查研究。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-12-31 DOI: 10.2196/77792
Melanie Mäder, Dirk Müller-Wieland, Tobias Wiesner, Tonio Schoenfelder, Carsta Militzer-Horstmann, Ria Heinrich, Mareike Geisler, Dennis Häckl
<p><strong>Background: </strong>In 2020, the global prevalence of overweight and obesity was approximately 42%. One of the most common associated conditions is type 2 diabetes mellitus, which had a global prevalence of around 10.5% in 2021. Digital health applications (DiHA), which can be prescribed as certified medical devices in Germany, have been shown to effectively support disease management in patients with overweight and diabetes mellitus. However, little is known about DiHA-prescribing behavior of health care providers (HCPs) specializing in hormones and metabolism or about potential barriers to prescribing these applications.</p><p><strong>Objective: </strong>This study aimed to assess HCPs' experience with and willingness to prescribe DiHA in the field of hormones and metabolism. In addition, it sought to examine the patient-relevant health care effects that HCPs perceive as potentially achievable or have already observed with DiHA use, as well as the barriers they perceive to prescribing these applications.</p><p><strong>Methods: </strong>An online questionnaire was developed based on preliminary studies and a literature review consisting of 86 items covering 6 key areas: experience and willingness to prescribe, health care effects, barriers, scientific evidence, digital affinity, and sociodemographics. The anonymous survey was distributed via the German Diabetes Association to 6035 HCPs in Germany between August 2 and October 9, 2024. Descriptive analyses, as well as correlation and regression analyses, were conducted.</p><p><strong>Results: </strong>A total of 350 HCPs participated in the survey (response rate=5.8%). Although the low response rate may limit generalizability, the findings provide insights into prescribing behavior within this specialty. More than half (187/350, 53.4%) had never prescribed any of the 54 DiHA available at the time of the survey, with 47.6% (89/187) citing a lack of experience as the primary reason. Among those who had prescribed a DiHA (163/350, 46.6%), the majority (139/163, 85.3%) had prescribed 1 of the 8 DiHA available for obesity or diabetes mellitus. Looking ahead, 42.9% (149/348) of all surveyed HCPs stated that they were either very unlikely (83/348, 23.9%) or somewhat unlikely (66/348, 19%) to prescribe these DiHA in the next 12 months. The greatest perceived benefits of DiHA were improvements in self-management, health literacy, and adherence. The main barriers to prescribing DiHA in the field of hormones and metabolism included inadequate reimbursement for ancillary medical services, poor compatibility with existing practice software, and a lack of digital affinity or motivation among patients.</p><p><strong>Conclusions: </strong>DiHA have not yet been fully integrated into standard health care. To improve prescribing, we recommend integrating DiHA into medical guidelines, ensuring proper reimbursement, and involving HCPs in the pricing and health-economic evaluation of DiHA. The recommendati
背景:2020年,全球超重和肥胖患病率约为42%。最常见的相关疾病之一是2型糖尿病,2021年全球患病率约为10.5%。数字健康应用程序(DiHA)在德国可作为经认证的医疗设备开处方,已被证明可有效支持超重和糖尿病患者的疾病管理。然而,关于专门从事激素和代谢的卫生保健提供者(HCPs)的diha处方行为或处方这些应用的潜在障碍所知甚少。目的:本研究旨在评估HCPs在激素和代谢领域使用DiHA的经验和意愿。此外,它还试图检查卫生保健专业人员认为使用DiHA可能实现或已经观察到的与患者相关的卫生保健效果,以及他们认为处方这些应用的障碍。方法:在初步研究和文献综述的基础上,编制了一份在线问卷,包括86个项目,涵盖6个关键领域:处方经验和意愿、卫生保健效果、障碍、科学证据、数字亲和力和社会人口统计学。这项匿名调查于2024年8月2日至10月9日期间通过德国糖尿病协会向德国6035名HCPs分发。进行描述性分析、相关分析和回归分析。结果:共有350名HCPs参与调查,应答率为5.8%。虽然低反应率可能会限制普遍性,但研究结果为该专业的处方行为提供了见解。超过一半(187/350,53.4%)的人在调查时从未开过54种DiHA中的任何一种,47.6%(89/187)的人认为缺乏经验是主要原因。在处方DiHA的患者中(163/350,46.6%),大多数(139/163,85.3%)处方了8种可用于肥胖或糖尿病的DiHA中的1种。展望未来,42.9%(149/348)的受访医务人员表示,他们在未来12个月内非常不可能(83/348,23.9%)或有点不可能(66/348,19%)开具这些DiHA。DiHA最大的好处是自我管理、健康素养和依从性的改善。在激素和代谢领域开DiHA处方的主要障碍包括辅助医疗服务报销不足,与现有实践软件兼容性差,以及患者缺乏数字亲和力或动机。结论:DiHA尚未完全纳入标准卫生保健。为了改善处方,我们建议将DiHA纳入医疗指南,确保适当的报销,并让卫生专业人员参与DiHA的定价和卫生经济评估。应考虑概述的建议,以最大限度地发挥DiHA的潜力,提高HCPs的接受度,为卫生政策提供有价值的见解,以加强DiHA的整合、报销和使用。
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引用次数: 0
Using a Proactive Telecare System to Support Independence, Health, and Well-Being in Older Adults: Feasibility Randomized Controlled Trial. 使用主动远程医疗系统支持老年人的独立性、健康和幸福感:可行性随机对照试验。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-12-31 DOI: 10.2196/82152
Lauren Fothergill, Yvonne Latham, Niall Hayes, Carol Holland
<p><strong>Background: </strong>Proactive telecare offers services designed to reduce the occurrence of emergency situations by delivering proactive outbound calls and follow-ups and providing information and advice. By engaging regularly with users, proactive telecare may foster social connections with older adults and enable the detection of changes in needs. Telecare systems that promote active participation among older adults may also foster feelings of autonomy and self-management.</p><p><strong>Objective: </strong>This study aimed to (1) explore the acceptability and feasibility of delivering and evaluating a proactive telecare intervention to community-dwelling older adults prior to a potential effectiveness trial and (2) evaluate the proposed eligibility criteria and estimate the potential effect size of the impact of the intervention on health and well-being outcomes to inform sample size calculations for a future trial.</p><p><strong>Methods: </strong>An 8-week randomized pre-post feasibility study was conducted. Using a mixed methods approach, questionnaires and semistructured interviews were used to explore the feasibility and acceptability of the study. The proactive telecare system encouraged users to press an OK button once a day to confirm their well-being. If they did not respond, participants received a well-being check, and emergency contacts were notified if required. Outcomes associated with independence, health, and well-being were measured using standardized questionnaires, including health-related quality of life, mental health, and loneliness.</p><p><strong>Results: </strong>Thirty older adults were recruited, with 13 randomized into the intervention group and 17 into the control group. The mean (SD) age of the participants was 75.4 (5.2) years; 66.7% (20/30) of the participants recruited had more than one health condition. This study achieved high retention rates (30/33, 90.9%); however, the expression of interest rate was low (52/295, 17.6%), indicating that changes to recruitment strategies are required. Effect sizes for all quantitative outcomes were small (approximately 0.2). Participants demonstrated high acceptance of the intervention, with the primary benefit cited as providing reassurance and promoting autonomy. Proactive engagement encouraged self-regulation and allowed users to control the level of support received. Those who were socially isolated reported feeling less lonely because of having additional social contact. Most participants felt the intervention would be particularly beneficial if they were experiencing poor health that significantly affected their daily activities, suggesting it may be more suited to those with limited independence. Some participants expressed anxiety about using the technology, primarily due to a lack of understanding and uncertainty in their perceived need for the device.</p><p><strong>Conclusions: </strong>This proactive telecare system is feasible to deliver within a cohort
背景:主动远程保健提供旨在减少紧急情况发生的服务,提供主动的外呼和后续行动以及提供信息和咨询。通过定期与用户接触,主动远程医疗可以促进与老年人的社会联系,并能够发现需求的变化。促进老年人积极参与的远程医疗系统也可能培养自主和自我管理的感觉。目的:本研究旨在(1)探索在潜在有效性试验之前向社区居住的老年人提供和评估主动远程医疗干预的可接受性和可行性;(2)评估拟议的资格标准,并估计干预对健康和福祉结果影响的潜在效应大小,为未来试验的样本量计算提供信息。方法:进行为期8周的随机前后可行性研究。采用混合方法,问卷调查和半结构化访谈来探讨研究的可行性和可接受性。主动远程医疗系统鼓励用户每天按一次OK键来确认他们的健康状况。如果他们没有回应,参与者会收到健康检查,如果需要,会通知紧急联系人。使用标准化问卷测量与独立性、健康和幸福感相关的结果,包括与健康相关的生活质量、心理健康和孤独感。结果:招募了30名老年人,其中13名随机分为干预组,17名随机分为对照组。参与者的平均(SD)年龄为75.4(5.2)岁;66.7%(20/30)的参与者有一种以上的健康状况。本研究获得了较高的保留率(30/33,90.9%);然而,利率的表达较低(52/295,17.6%),表明需要改变招聘策略。所有定量结果的效应值都很小(约为0.2)。参与者表现出对干预的高度接受度,主要的好处是提供了保证和促进了自主性。主动参与鼓励自我调节,并允许用户控制所获得的支持水平。那些被社会孤立的人报告说,由于有了额外的社会接触,他们感到不那么孤独。大多数参与者认为,如果他们的健康状况不佳,严重影响了他们的日常活动,这种干预将特别有益,这表明它可能更适合那些独立性有限的人。一些参与者表达了对使用该技术的焦虑,主要是由于缺乏理解和不确定他们对该设备的感知需求。结论:这种主动远程医疗系统是可行的,提供了一个队列的老年人生活在社区。但是,需要改变征聘方法和执行情况,以确保在今后的有效性试验中可接受性和达到目标数字。
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引用次数: 0
Quality Assessment of Shock Videos on Video Sharing Platforms: Cross-Sectional Study. 视频分享平台冲击视频质量评估:横断面研究
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-12-30 DOI: 10.2196/76715
Wenxin Wang, Luping Cheng, Xia Hu, Chuanliang Pan

Background: As a highly lethal circulatory failure syndrome, the pathophysiological mechanisms of shock can lead to multiple organ dysfunction syndrome (MODS), which significantly increases the demand for intensive care and the length of hospitalization. There is therefore an urgent need for the public to be informed about health-related issues. In recent years, videos have become a significant medium for health education, and this study aimed to evaluate shock-related videos on video sharing platforms.

Objective: The objective of this study is to identify the top 100 videos related to impact on TikTok, Bilibili, and Xiaohongshu. These videos will then be assessed in terms of their effectiveness and credibility. Following this evaluation, relevant recommendations will be provided.

Methods: The study included a search for videos related to shock on the three video-sharing platforms: TikTok, Bilibili, and Xiaohongshu. The Global Quality Score (GQS) and mDISCERN tools were used to evaluate the credibility and quality of the videos, in addition to employing the Patient Education Materials Evaluation Tool for Audiovisual Content (PEMAT-A/V). Finally, the video was evaluated by examining disease definitions, clinical manifestations, risk factors, assessment, management, and outcomes.

Results: A total of 244 videos (TikTok:87, Bilibili:80, Xiaohongshu:77)were retrieved from the three platforms. The overall video quality was found to be moderately low. The majority of videos were uploaded by health advocates (n=102, 41.8%) and health professionals (n=98, 40.1%). The individual video sources of the GQS were of lower quality (1-3), the mDISCERN scores were moderate (2-4), and the quality of individual users is higher than that of organizational users. The PEMAT A/V scores were as follows: in the overall comprehensibility evaluation, 91% (220) videos of the scores were above 70%; in the actionability evaluation, 65% (157) videos of the scores were below 70%. It should be noted that the actionability scores for different video sources were generally low. In 172 videos (70.4%), the definition of shock and its clinical manifestations were explained in detail, while in 137 videos (56.1%), the definition of shock and its clinical manifestations were also clearly explained. The majority of videos provided a relatively comprehensive explanation of the definition of shock and its clinical signs and symptoms.

Conclusions: Our study have demonstrated that the content and information quality of shock videos is unsatisfactory, as a general rule. This underscores the necessity for pertinent regulatory bodies to oversee the caliber of health-related videos, and for content creators to enhance the quality of their content.

背景:休克作为一种高致死率的循环衰竭综合征,其病理生理机制可导致多器官功能障碍综合征(MODS),显著增加重症监护需求和住院时间。因此,迫切需要让公众了解与健康有关的问题。近年来,视频已成为健康教育的重要媒介,本研究旨在评估视频分享平台上与休克相关的视频。目的:本研究的目的是确定在抖音、哔哩哔哩和小红书上影响最大的100个视频。然后将对这些录像的有效性和可信性进行评估。在此评估之后,将提出相关建议。方法:研究包括在三个视频分享平台:抖音、哔哩哔哩和小红书上搜索与休克相关的视频。除了使用患者教育材料视听内容评估工具(PEMAT-A/V)外,还使用全球质量评分(GQS)和mDISCERN工具来评估视频的可信度和质量。最后,通过检查疾病定义、临床表现、危险因素、评估、管理和结果对视频进行评估。结果:三个平台共检索视频244个,其中抖音87个,哔哩哔哩80个,小红书77个。整体视频质量一般较低。上传视频的主要是健康倡导者(n=102, 41.8%)和卫生专业人员(n=98, 40.1%)。GQS的个人视频源质量较低(1-3),mDISCERN得分中等(2-4),个人用户的质量高于组织用户。PEMAT的A/V得分情况如下:在整体可理解性评价中,91%(220个)的视频得分在70%以上;在可操作性评价中,65%(157)的视频得分低于70%。应该指出的是,不同视频源的可操作性得分普遍较低。172个视频(70.4%)对休克的定义及其临床表现进行了详细的解释,137个视频(56.1%)对休克的定义及其临床表现进行了明确的解释。大多数视频对休克的定义及其临床体征和症状提供了相对全面的解释。结论:我们的研究表明,一般情况下,震惊视频的内容和信息质量令人不满意。这强调了相关监管机构监督与健康相关视频质量的必要性,以及内容创作者提高其内容质量的必要性。
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引用次数: 0
Feasibility and Usability of an mHealth App (mLab+) to Guide Users Through HIV and Syphilis Self-Testing: Pilot Randomized Controlled Trial. 移动健康应用程序(mLab+)指导用户进行艾滋病毒和梅毒自我检测的可行性和可用性:试点随机对照试验。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-12-30 DOI: 10.2196/72955
Maeve Brin, Thomas F Scherr, Janejira Chaiyasit, Jianfang Liu, Maura Abbott, Robert Garofalo, Lisa M Kuhns, Tess Sky, Ian Esliker, Rebecca Schnall

Background: HIV self-testing is an important strategy in the US Ending the HIV Epidemic initiative. To facilitate uptake of self-testing, we developed the mLab app, which complements existing self-test options to support the potential for higher uptake of the HIV self-test. Syphilis, a sexually transmitted infection with currently rising prevalence and overlap in risk profiles with HIV, could similarly benefit from the advantages of companion diagnostic mobile apps such as mLab. Due to the success of the mLab app in promoting HIV self-testing during a randomized controlled trial and the scientific evidence of need for at-home syphilis testing, our team developed the mLab+ app, which supports both HIV and syphilis testing through an image processing algorithm that incorporates a duplex HIV and syphilis point-of-care test.

Objective: We conducted a pilot study to assess the feasibility and usability of the mLab+ app for HIV and syphilis testing.

Methods: We recruited participants who were assigned male sex at birth and reported sex with another man. Participants came to the Nurse Practitioner Group clinic for baseline and follow-up visits. Participants rated the usability of the app using the Health Information Technology Usability Evaluation Scale and the Post-Study System Usability Questionnaire at their 3-month follow-up visit. The primary outcome was the number of participants who were able to self-administer the DPP HIV-Syphilis test with the assistance of the mLab+ app. Feasibility was measured through recruitment pace, retention over 3 months, app usability, and paradata.

Results: Of the 20 participants, 19 identified as male and 1 identified as nonbinary. Most participants (n=16) were able to complete the DPP HIV-Syphilis test with facilitation support from the mLab+ app. The average duration of an app session, from after authentication until log-out or abandonment, was 30 minutes and 33 seconds (SD 21 minutes and 40 seconds). Apart from the 27% (13/48) of sessions that were 5 minutes or less, the distribution of session durations was approximately normal. Users spent the longest time viewing testing screens (ie, timer screens, initial testing screen, test guided walkthroughs, test results, and picture and result upload). The overall mean scores on the Post-Study System Usability Questionnaire (2.65, SD 1.06) and Health Information Technology Usability Evaluation Scale (3.62, SD 1.07) indicated medium to high usability. The retention rate for the 3-month trial was 80% (16/20).

Conclusions: The findings support the use of the mLab+ app as a tool for assisting consumers in self-testing for HIV and syphilis. The limitations of the study design warrant further examination outside of clinic settings to better understand the utility of these tools for improving consumer health outcomes.

背景:艾滋病毒自我检测是美国结束艾滋病毒流行倡议的一项重要战略。为了促进自检的接受,我们开发了mLab应用程序,它补充了现有的自检选项,以支持更高的艾滋病毒自检接受率。梅毒是一种性传播感染,目前发病率不断上升,其风险与艾滋病毒有重叠,同样也可以从mLab等配套诊断移动应用程序的优势中受益。由于mLab应用程序在随机对照试验中促进艾滋病毒自我检测的成功以及需要在家进行梅毒检测的科学证据,我们的团队开发了mLab+应用程序,该应用程序通过包含双重艾滋病毒和梅毒护理点检测的图像处理算法支持艾滋病毒和梅毒检测。目的:我们进行了一项初步研究,以评估mLab+应用程序用于HIV和梅毒检测的可行性和可用性。方法:我们招募了出生时被指定为男性并报告与另一名男性发生过性关系的参与者。参与者来到执业护士小组诊所进行基线和随访。参与者在三个月的随访中使用健康信息技术可用性评估量表和研究后系统可用性问卷对应用程序的可用性进行评分。主要结果是能够在mLab+应用程序的帮助下自行进行DPP hiv -梅毒检测的参与者数量。可行性通过招募速度、3个月以上的保留率、应用程序可用性和para来衡量。结果:在20名参与者中,19名确定为男性,1名确定为非二元性别。大多数参与者(n=16)能够在mLab+应用程序的协助支持下完成DPP hiv -梅毒测试。从认证后到退出或放弃,应用程序会话的平均持续时间为30分33秒(SD为21分40秒)。除了27%(13/48)的会话为5分钟或更短,会话持续时间的分布大致为正态分布。用户花费最长的时间观看测试屏幕(即计时器屏幕、初始测试屏幕、测试指导演练、测试结果、图片和结果上传)。研究后系统可用性问卷(2.65,SD 1.06)和健康信息技术可用性评估量表(3.62,SD 1.07)的总体平均得分为中高可用性。3个月的保留率为80%(16/20)。结论:研究结果支持使用mLab+应用程序作为帮助消费者自我检测艾滋病毒和梅毒的工具。由于研究设计的局限性,需要在临床环境之外进行进一步的检查,以更好地了解这些工具在改善消费者健康结果方面的效用。
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引用次数: 0
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