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Preferences for an Experience Sampling Method-Based Tool as an Adjunct to Usual Treatment in Patients With Problem Substance Use: Qualitative Study. 对经验抽样方法为基础的工具的偏好,作为问题物质使用患者常规治疗的辅助:定性研究。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-01-15 DOI: 10.2196/79510
Adam Kurilla, Natália Čavojská, Theresa Ikegwuonu, Marta Nemčíková, Julia Cc Schulte-Strathaus, Lotte Uyttebroek, Joanne R Beames, Dagmar Breznoščáková, Daniel Dančík, Michal Hajdúk, Anton Heretik, Ľubomíra Izáková, Zuzana Katreniaková, Inez Myin-Germeys, Ján Pečeňák, Ulrich Reininghaus, Anita Schick, Maria Wolters

Background: Mobile health tools that use the Experience Sampling Method (ESM) appear to be a promising tool to streamline and improve the treatment of substance use disorders. However, patient involvement in the development of these tools is uncommon, and research on the preferences of people being treated for substance use disorders has been scarce. In the scope of the European Union IMMERSE (Implementing Mobile Mental health Recording Strategy for Europe) consortium, an ESM-based tool for Digital Mobile Mental Health (DMMH) was first codeveloped and later tested in 4 European countries.

Objective: This study aimed to achieve an understanding of preferences for features of DMMH among mental health service users with problem substance use.

Methods: In 4 European countries, service users were recruited for a semistructured qualitative interview, which started with the presentation of a prototype of the DMMH. Data analysis was performed through directed qualitative content analysis.

Results: The analytical sample consisted of 12 (5 female, 6 male, and 1 nonbinary person) participants with problem substance use aged 18-50 years. There were 4 participants from Slovakia, 3 from Belgium, 4 from Germany, and 1 from Scotland. Patient preferences were classified into 7 categories: notifications, questions, user interface, functionality changes, visualizations, sharing data with clinicians, and sharing data with others. The proposed intensive notification schedule was deemed acceptable by service users as long as the questionnaire is short. Participants expressed a preference for open-text response options, Ecological Momentary Interventions, and options for individual customization of several elements of the tool. Data visualization was considered an important aid for communication with clinicians, with whom all participants wanted to share data obtained with DMMH. The possibility of sharing data with other people depended on the quality of the relationship with them.

Conclusions: In the development of ESM-based mobile health tools for people with problem substance use, their preferences for content, functionality, and appearance of the tools should be considered so they match patients' treatment needs.

背景:使用经验抽样方法(ESM)的移动卫生工具似乎是简化和改善物质使用障碍治疗的有前途的工具。然而,患者参与这些工具的开发并不常见,并且对正在接受药物使用障碍治疗的人的偏好的研究很少。在欧洲联盟实施欧洲流动精神卫生记录战略联盟的范围内,首先共同开发了一种基于esm的数字流动精神卫生(DMMH)工具,后来在4个欧洲国家进行了测试。目的:本研究旨在了解有问题物质使用的精神卫生服务使用者对DMMH特征的偏好。方法:在4个欧洲国家,招募了服务用户进行半结构化定性访谈,首先介绍了DMMH的原型。通过直接定性内容分析进行数据分析。结果:分析样本包括12名年龄在18-50岁的问题物质使用参与者(女性5人,男性6人,非二元人格1人)。斯洛伐克4人,比利时3人,德国4人,苏格兰1人。患者偏好分为7类:通知、问题、用户界面、功能变化、可视化、与临床医生共享数据以及与他人共享数据。只要问卷短,服务用户认为建议的密集通知时间表是可以接受的。参与者表达了对开放文本响应选项、生态瞬时干预和工具若干元素的个人定制选项的偏好。数据可视化被认为是与临床医生沟通的重要辅助手段,所有参与者都希望与临床医生共享从DMMH获得的数据。与他人共享数据的可能性取决于与他们关系的质量。结论:在为问题物质使用人群开发基于esm的移动健康工具时,应考虑他们对工具内容、功能和外观的偏好,以便与患者的治疗需求相匹配。
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引用次数: 0
Contribution of an Online Intervention to Developing Communities of Practice: Mixed Methods Evaluation of an Online Safety Hub to Address Harmful Online Content in Relation to Self-Harm and Suicide. 在线干预对发展实践社区的贡献:在线安全中心解决与自我伤害和自杀有关的有害在线内容的混合方法评估。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-01-14 DOI: 10.2196/72130
Arne Mueller, Gemma Hughes, Gregory Maniatopoulos

Background: Online harm affects many people and has been associated with self-harm and suicidal ideation. Although there is an emerging body of evidence that addressing adverse online experiences should be part of the support offered to people who are at risk of self-harm and suicide, there has been little guidance to date on how this support might be provided and how safe conversations can be had on the subject. A UK charity dedicated to offering emotional support to anyone experiencing mental discomfort, having difficulty coping, or being at risk of suicide developed a digital intervention, the Online Safety Hub (the Hub), to address this shortfall.

Objective: The study aimed to evaluate the impact of the Hub on practitioners (people who provide support) and people with lived experiences of suicide and self-harm and to determine what learning environment is best suited to increase and maintain learning in the context of the Hub.

Methods: A sequential explanatory mixed methods evaluation comprised a rapid literature review, data collected from people with lived experience (n=6) and practitioners through an analysis of the Hub's activity data, 2 surveys (survey 1: n=45; survey 2: n=368), interviews (n=9), and focus groups (n=7). Surveys were analyzed for descriptive purposes only, and the interview and focus group analyses comprised coding of data and thematic analysis. The study design was informed by a panel of people with lived experience of online harm resulting in either self-harm and/or suicidal ideation.

Results: Initially, the evaluation found limited uptake of the Hub. Engagement with the Hub was impeded by a lack of clarity on the part of practitioners as to whether they were the intended audience. The evaluation process prompted the charity to design and deliver webinars to facilitate uptake of the Hub. Practitioners who engaged with the Hub via webinars found the content useful and were able to consider incorporating their learning into practice. The webinars offered a more social learning experience than individual engagement with the Hub, providing a community of practice for people with common interests across diverse organizational settings. Opportunities for shared learning and the supportive nature of the community of practice were valued when learning about the sensitive and difficult topic of online harm in relation to self-harm and suicide. The Hub contributed to awareness-raising and shared learning.

Conclusions: Online resources alone may not be sufficient for an intervention to effectively raise awareness and change practice. Social learning facilitated through communities of practice can enhance engagement, uptake, and learning.

背景:网络伤害影响到许多人,并与自我伤害和自杀意念有关。尽管有越来越多的证据表明,解决不良的网络经历应该成为向有自残和自杀风险的人提供支持的一部分,但迄今为止,关于如何提供这种支持以及如何安全地就这个话题进行对话的指导很少。一家英国慈善机构致力于为任何经历精神不适、难以应对或有自杀风险的人提供情感支持,为了解决这一不足,他们开发了一种数字干预手段——在线安全中心(Hub)。目的:本研究旨在评估中心对从业人员(提供支持的人)和有自杀和自残生活经历的人的影响,并确定哪种学习环境最适合在中心的背景下增加和维持学习。方法:顺序解释性混合方法评估包括快速文献综述,从有生活经验的人(n=6)和通过分析中心活动数据收集的从业者中收集的数据,2项调查(调查1:n=45;调查2:n=368),访谈(n=9)和焦点小组(n=7)。调查的分析仅用于描述目的,访谈和焦点小组分析包括数据编码和专题分析。这项研究的设计是由一组有过网络伤害经历的人提供的,这些人要么会自残,要么会产生自杀念头。结果:最初,评估发现对Hub的吸收有限。由于从业者不清楚他们是否是目标受众,因此阻碍了与该中心的接触。评估过程促使慈善机构设计和举办网络研讨会,以促进对中心的吸收。通过网络研讨会参与Hub的从业者发现内容很有用,并且能够考虑将他们的学习融入实践。网络研讨会提供了比个人参与Hub更社会化的学习体验,为不同组织环境中有共同兴趣的人提供了一个实践社区。在了解与自我伤害和自杀相关的在线伤害这一敏感和困难的话题时,共享学习的机会和实践社区的支持性质受到重视。该中心有助于提高认识和共享学习。结论:在线资源本身可能不足以进行干预,以有效地提高认识和改变做法。通过实践社区促进的社会学习可以增强参与、吸收和学习。
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引用次数: 0
Evaluating the Efficacy of AI-Based Interactive Assessments Using Large Language Models for Depression Screening: Development and Usability Study. 使用大型语言模型评估基于人工智能的抑郁症筛查互动评估的有效性:开发和可用性研究。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-01-13 DOI: 10.2196/78401
Zheng Jin, Jiaxing Hu, Dandan Bi, Kaibin Zhao, Huan Yu

Background: The evolution of language models, particularly large language models, has introduced transformative potential for psychological assessment, challenging traditional rating scale methods that have dominated clinical practice for over a century.

Objective: This study aimed to develop and validate an automated assessment paradigm that integrates natural language processing with conventional measurement tools to assess depressive symptoms, exploring its feasibility as a novel approach in psychological evaluation.

Methods: A cohort of 115 participants, including 28 (24.3%) individuals diagnosed with depression, completed the Beck Depression Inventory Fast Screen via a custom ChatGPT interface (BDI-FS-GPT) and the Chinese version of the Patient Health Questionnaire-9 (PHQ-9). Statistical analyses included the Spearman correlation (PHQ-9 vs BDI-FS-GPT scores), Cohen κ (diagnostic agreement), and area under the curve (AUC) evaluation.

Results: Spearman analysis revealed a moderate correlation between PHQ-9 and BDI-FS-GPT scores. The Cohen κ indicated moderate diagnostic agreement between the PHQ-9 and the BDI-FS-GPT (κ=0.43; 76.5% agreement), substantial agreement between the BDI-FS-GPT and the clinical diagnosis (κ=0.72; 88.7% agreement), and moderate agreement between the PHQ-9 and the clinical diagnosis (κ=0.55; 71.4% agreement). The BDI-FS-GPT demonstrated excellent diagnostic accuracy (AUC=0.953) at a cutoff of 3, detecting 89.3% of participants with depression with an 11.5% false-positive rate compared to the PHQ-9 (AUC=0.859) at a cutoff of 5 (sensitivity=71.4%; false-positive rate=13.8%). Participants also reported significantly higher satisfaction with the automated assessment compared to the traditional scale (P=.02).

Conclusions: The automated assessment paradigm framework combines the interactivity and personalization of natural language processing-powered tools with the psychometric rigor of traditional scales, suggesting a preliminary feasibility paradigm for future psychological assessment. Its ability to enhance engagement while maintaining reliability and validity provides encouraging evidence, warranting validation in larger and more diverse studies as large language model technology advances.

International registered report identifier (irrid): RR2-10.1101/2024.07.19.24310543.

背景:语言模型的发展,特别是大型语言模型的发展,为心理评估带来了变革潜力,挑战了一个多世纪以来主导临床实践的传统评定量表方法。目的:本研究旨在开发和验证一种将自然语言处理与传统测量工具相结合的抑郁症状自动评估范式,探索其作为一种新的心理评估方法的可行性。方法:115名参与者,其中28名(24.3%)被诊断为抑郁症,通过自定义ChatGPT界面(BDI-FS-GPT)和中文版患者健康问卷-9 (PHQ-9)完成贝克抑郁量表快速筛选。统计分析包括Spearman相关性(PHQ-9与BDI-FS-GPT评分)、Cohen κ(诊断一致性)和曲线下面积(AUC)评估。结果:Spearman分析显示PHQ-9与BDI-FS-GPT评分有中度相关性。Cohen κ表明PHQ-9与BDI-FS-GPT的诊断一致(κ=0.43,一致性76.5%),BDI-FS-GPT与临床诊断一致(κ=0.72,一致性88.7%),PHQ-9与临床诊断一致(κ=0.55,一致性71.4%)。BDI-FS-GPT在截断值为3时显示出出色的诊断准确性(AUC=0.953),与PHQ-9 (AUC=0.859)在截断值为5时(灵敏度=71.4%,假阳性率=13.8%)相比,检测出89.3%的抑郁症参与者,假阳性率为11.5%。与传统量表相比,参与者对自动评估的满意度也显著提高(P= 0.02)。结论:自动评估范式框架将自然语言处理工具的交互性和个性化与传统量表的心理测量严谨性相结合,为未来的心理评估提供了初步的可行性范式。它在保持可靠性和有效性的同时增强参与度的能力提供了令人鼓舞的证据,保证随着大型语言模型技术的进步,在更大、更多样化的研究中得到验证。国际注册报告标识符(irrid): RR2-10.1101/2024.07.19.24310543。
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引用次数: 0
Survey Evaluation of the Role of Social Media and Social Support for Transgender, Nonbinary, and Intersex People: Observational Study. 社会媒体对跨性别、非二元性和双性人社会支持作用的调查评估:观察性研究。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-01-13 DOI: 10.2196/79614
Krishnan Nayar, Vivian C Iloabuchi, Juliana M Kling, Bithika Thompson, Christopher Dodoo, Robert Horsley
<p><strong>Background: </strong>Transgender and gender-diverse (TGD) people experience greater health disparities than their cisgender counterparts. Social determinants of health are linked to these health disparities in minority communities, including the TGD community. Lack of social support contributes significantly to these disparities for the TGD community.</p><p><strong>Objective: </strong>The aim of this study was to evaluate the role of social media and social support groups among TGD patients who attend a transgender clinic.</p><p><strong>Methods: </strong>A questionnaire was developed through an iterative process and emailed to TGD people attending a tertiary care TGD-focused clinic. The survey assessed social media use (platforms, duration, and adverse effects), social support groups (past participation and interest in current participation), and demographic characteristics (age, gender, race and ethnicity, educational level, religious affiliation, and income).</p><p><strong>Results: </strong>Our survey garnered 48 responses. Of these participants, 50% (n=24) identified as transfeminine or transgender women, 29.2% (n=14) identified as transmasculine or transgender men, 8.3% (n=4) identified as nonbinary, 2.1% (n=1) identified as genderfluid, and 10.4% (n=5) identified as another identity. Our respondents' average age was 35 (SD 15.6) years. Nearly 70% (n=31, 64.6%) reported at least monthly transphobia, and 35.4% (n=17) reported at least weekly transphobia. Primary social support was reported as coming from an in-person significant other or friend 49% (n=24) of the time and from social media or online friends 12.5% (n=6) of the time. Social media was used for the primary purpose of interacting with queer or TGD people by 65% (n=33) of respondents, and the most common sites used were Discord, Reddit, and Instagram. Among respondents who either were attending or had attended a gender identity-focused support group, 61% (14/23) reported them being beneficial. In total, 52% (25/48) had never attended a support group related to their gender identity, and 60% (15/23) were open to attending.</p><p><strong>Conclusions: </strong>This study found that social media is already being used by TGD people for the purpose of interacting with other queer and transgender people but also that there are risks associated with its use. Given this reality, counseling patients on social media use should focus on safety in use and honest discussions of both the risks and benefits associated with its use. Regarding social support groups focused on gender identity, many current or previous attendants reported that support groups were helpful for finding social support, especially early on in one's transition and when other avenues of support are not present. Additionally, many respondents who had never attended a support group were interested in attending for the perceived benefits of increased social support and interest in meeting other community members. Engag
背景:跨性别和性别多样化(TGD)的人比他们的顺性别同行经历更大的健康差异。健康的社会决定因素与少数民族社区,包括TGD社区的这些健康差异有关。缺乏社会支持在很大程度上导致了TGD社区的这些差异。目的:本研究的目的是评估社交媒体和社会支持团体在参加变性诊所的TGD患者中的作用。方法:通过迭代过程开发一份问卷,并通过电子邮件发送给参加三级保健TGD重点诊所的TGD患者。该调查评估了社交媒体的使用(平台、持续时间和负面影响)、社会支持团体(过去参与和对当前参与的兴趣)和人口特征(年龄、性别、种族和民族、教育水平、宗教信仰和收入)。结果:我们的调查获得了48份回复。在这些参与者中,50% (n=24)被确定为跨女性或跨性别女性,29.2% (n=14)被确定为跨男性或跨性别男性,8.3% (n=4)被确定为非二元性别,2.1% (n=1)被确定为性别流体,10.4% (n=5)被确定为其他身份。受访者的平均年龄为35岁(标准差15.6)。近70% (n=31, 64.6%)报告至少每月有跨性别恐惧症,35.4% (n=17)报告至少每周有跨性别恐惧症。据报道,主要的社会支持来自面对面的重要他人或朋友49% (n=24),来自社交媒体或在线朋友12.5% (n=6)。65% (n=33)的受访者使用社交媒体的主要目的是与酷儿或变性人互动,最常用的网站是Discord、Reddit和Instagram。在正在参加或曾经参加过以性别认同为中心的支持小组的受访者中,61%(14/23)的人表示他们是有益的。总共有52%(25/48)的人从未参加过与他们的性别认同有关的支持小组,60%(15/23)的人愿意参加。结论:这项研究发现,TGD人群已经在使用社交媒体与其他酷儿和变性人进行互动,但使用社交媒体也存在风险。鉴于这一现实,对患者使用社交媒体的咨询应侧重于使用安全性,并诚实地讨论与使用社交媒体相关的风险和益处。关于关注性别认同的社会支持小组,许多现任或以前的参与者报告说,支持小组有助于找到社会支持,特别是在一个人的过渡早期和其他支持途径不存在的时候。此外,许多从未参加过支持小组的受访者对参加支持小组感兴趣,因为他们认为可以增加社会支持,并有兴趣与其他社区成员会面。让TGD患者参与使用社交媒体和社会支持团体来获得性别认同,可能有助于提高对他们的支持,尽管使用社交媒体会带来仇恨和跨性别恐惧症的风险。
{"title":"Survey Evaluation of the Role of Social Media and Social Support for Transgender, Nonbinary, and Intersex People: Observational Study.","authors":"Krishnan Nayar, Vivian C Iloabuchi, Juliana M Kling, Bithika Thompson, Christopher Dodoo, Robert Horsley","doi":"10.2196/79614","DOIUrl":"10.2196/79614","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;Transgender and gender-diverse (TGD) people experience greater health disparities than their cisgender counterparts. Social determinants of health are linked to these health disparities in minority communities, including the TGD community. Lack of social support contributes significantly to these disparities for the TGD community.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;The aim of this study was to evaluate the role of social media and social support groups among TGD patients who attend a transgender clinic.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;A questionnaire was developed through an iterative process and emailed to TGD people attending a tertiary care TGD-focused clinic. The survey assessed social media use (platforms, duration, and adverse effects), social support groups (past participation and interest in current participation), and demographic characteristics (age, gender, race and ethnicity, educational level, religious affiliation, and income).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;Our survey garnered 48 responses. Of these participants, 50% (n=24) identified as transfeminine or transgender women, 29.2% (n=14) identified as transmasculine or transgender men, 8.3% (n=4) identified as nonbinary, 2.1% (n=1) identified as genderfluid, and 10.4% (n=5) identified as another identity. Our respondents' average age was 35 (SD 15.6) years. Nearly 70% (n=31, 64.6%) reported at least monthly transphobia, and 35.4% (n=17) reported at least weekly transphobia. Primary social support was reported as coming from an in-person significant other or friend 49% (n=24) of the time and from social media or online friends 12.5% (n=6) of the time. Social media was used for the primary purpose of interacting with queer or TGD people by 65% (n=33) of respondents, and the most common sites used were Discord, Reddit, and Instagram. Among respondents who either were attending or had attended a gender identity-focused support group, 61% (14/23) reported them being beneficial. In total, 52% (25/48) had never attended a support group related to their gender identity, and 60% (15/23) were open to attending.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;This study found that social media is already being used by TGD people for the purpose of interacting with other queer and transgender people but also that there are risks associated with its use. Given this reality, counseling patients on social media use should focus on safety in use and honest discussions of both the risks and benefits associated with its use. Regarding social support groups focused on gender identity, many current or previous attendants reported that support groups were helpful for finding social support, especially early on in one's transition and when other avenues of support are not present. Additionally, many respondents who had never attended a support group were interested in attending for the perceived benefits of increased social support and interest in meeting other community members. Engag","PeriodicalId":14841,"journal":{"name":"JMIR Formative Research","volume":"10 ","pages":"e79614"},"PeriodicalIF":2.0,"publicationDate":"2026-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12798915/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145966299","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
Exploring Perceived Changes to Mental Health When Restricting and Resuming Specific Adaptive Daily Actions: Longitudinal Qualitative Substudy Within a Randomized Controlled Trial. 当限制和恢复特定的适应性日常行为时,探索心理健康的感知变化:随机对照试验中的纵向定性亚研究。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-01-13 DOI: 10.2196/82986
Alana Fisher, Blake F Dear, Alison Dagnall, Heather D Hadjistavropoulos, Olav Nielssen, Lauren G Staples, Rony Kayrouz, Nickolai Titov
<p><strong>Background: </strong>Anxiety and depressive disorders are common and burdensome, yet many people prefer to self-manage and do not access treatment or fail to achieve meaningful improvement. Prior research indicates that the frequency of performing simple, everyday actions, namely "The Things You Do" (TYD; ie, healthy thinking, meaningful activities, having goals and plans, healthy routines, and social connection), is strongly associated with support mental health and well-being. This research has been primarily quantitative in nature, and so less is known about how people perceive and interpret changes in their mental health when engaging in or limiting these actions.</p><p><strong>Objective: </strong>This study aims to explore participants' perceptions of mental health changes and associated insights into what most impacts their mental health, during a randomized controlled trial involving the systematic restriction and followed by the resumption of the TYD actions.</p><p><strong>Methods: </strong>This longitudinal qualitative substudy analyzed weekly free-text comments from 70 healthy Australian adults (intervention group [IG] n=36; control group [CG] n=34). IG participants completed an 8-week randomized controlled trial comprising 3 phases: a 2-week baseline phase (Phase A), a 2-week behavior restriction phase during which they reduced the frequency of the TYD actions (Phase B), and a 4-week recovery or resumption phase during which they increased the frequency of the TYD actions back to usual levels (Phase C). CG participants were instructed to maintain usual habits and activities. The weekly free-text comments were related to what participants had noticed and learned about their mental health. These were thematically analyzed using framework methods to identify patterns in perceived changes, considering trial phase, group allocation, and participant characteristics.</p><p><strong>Results: </strong>Analyses identified five interrelated themes around what participants reportedly learned and what most impacted their mental health: (1) rhythms of daily life and routine, (2) harnessing internal psychological resources, (3) social support and interpersonal stressors, (4) staying active and enjoying yourself, and (5) environmental and external influences. In the IG, participants reported that behavioral restriction led to subjective disruptions across all 5 themes, precipitating declines in mood, energy, and stability; resumption fostered recovery, along with increased insights into oneself and mental health, coping strategies, and a sense of agency. Compared to the IG, the CG more often emphasized environmental and external influences.</p><p><strong>Conclusions: </strong>The findings reinforce the centrality of specific daily actions, namely the TYD, to people's subjective well-being and suggest an additional "macro-level" comprising environmental and external influences. Exposure to behavioral restriction and resumption/recovery served
背景:焦虑和抑郁障碍是常见和繁重的,但许多人更喜欢自我管理,不接受治疗或未能实现有意义的改善。先前的研究表明,执行简单的日常行动的频率,即“你做的事情”(TYD,即健康的思维,有意义的活动,有目标和计划,健康的日常活动和社会联系),与支持心理健康和福祉密切相关。这项研究本质上主要是定量的,因此人们在参与或限制这些行为时如何感知和解释他们心理健康的变化,我们所知甚少。目的:本研究旨在通过一项随机对照试验,探讨被试对心理健康变化的看法,以及对影响其心理健康的因素的相关见解,该试验包括系统限制和随后恢复的TYD行为。方法:本纵向定性亚研究分析了70名澳大利亚健康成年人每周的自由文本评论(干预组[IG] n=36;对照组[CG] n=34)。IG参与者完成了一项为期8周的随机对照试验,包括3个阶段:2周的基线阶段(a阶段),2周的行为限制阶段,在此期间他们减少了TYD行为的频率(B阶段),以及4周的恢复或恢复阶段,在此期间他们将TYD行为的频率增加到正常水平(C阶段)。CG参与者被要求保持正常的习惯和活动。每周的自由文本评论与参与者注意到和了解到的关于他们心理健康的内容有关。考虑到试验阶段、分组分配和参与者特征,使用框架方法对这些结果进行主题分析,以确定感知变化的模式。结果:分析确定了五个相互关联的主题,围绕参与者报告的学习内容和最影响他们心理健康的因素:(1)日常生活和常规节奏,(2)利用内部心理资源,(3)社会支持和人际压力源,(4)保持活跃和享受自己,以及(5)环境和外部影响。在IG中,参与者报告说,行为限制导致所有5个主题的主观干扰,导致情绪、精力和稳定性的下降;复工促进了康复,同时也增加了对自己和心理健康、应对策略和代理感的洞察力。与IG相比,CG更经常强调环境和外部影响。结论:研究结果强化了具体的日常行为(即TYD)对人们主观幸福感的中心地位,并提出了一个额外的“宏观层面”,包括环境和外部影响。接触行为限制和恢复/恢复有助于突出某些因素对心理健康的重要性,并似乎改善了人们对其心理健康的能动性和控制点的感觉。
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引用次数: 0
Expanding the Digital, Donor-Assisted Conception Tool to Empower Parental Telling and Talking (TELL Tool) Intervention to the Pregnant and Early Parenthood Periods: Findings From a Qualitative Study. 扩大数字,捐助者辅助受孕工具,以授权父母告诉和谈话(TELL工具)干预怀孕和早期父母时期:来自定性研究的结果。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-01-13 DOI: 10.2196/79024
Patricia E Hershberger, Kirby Adlam, Mary B Richardson, Alison L Miller, Chelsea Fortin, Martha Driessnack, Harold D Grotevant, Susan C Klock, Lauri A Pasch, Agatha M Gallo
<p><strong>Background: </strong>Many parents who use donor-assisted conception to form their families struggle with telling their children about how they came to be. To address this problem, we created the Tool to Empower Parental Telling and Talking (TELL Tool), a digital, psychoeducational, and decision-support intervention for parents with children aged 1 to 16 years. Recently, we completed a pilot randomized controlled trial of the TELL Tool that showed feasibility, acceptability, and promise. However, in its current version, the TELL Tool does not include content for pregnant, expecting, or new parents with children less than 1 year of age.</p><p><strong>Objective: </strong>The aim of this formative study was to understand the views of pregnant, expecting, and new parents who used donor-assisted conception to form their families, along with the views of practicing clinicians about disclosure to expand the TELL Tool for use during the pregnant and early parenthood periods in the United States.</p><p><strong>Methods: </strong>Using a qualitative descriptive approach, a purposive sample of 20 parents and 10 practicing clinicians was recruited using a multifaceted recruitment plan. Each participant completed an in-depth, semistructured interview over Zoom that was recorded, auto-transcribed, checked for accuracy, and subsequently analyzed for themes. The rigorous and accelerated data reduction technique was incorporated into the analytic plan.</p><p><strong>Results: </strong>Parents comprised pregnant (n=6) or new parents (n=15), as one parent was both pregnant and had a child less than 24 months of age. The 10 clinicians, consisting of an array of multidisciplinary health care professionals, were practicing in fertility/infertility (n=4), obstetrics and women's health (n=3), and reproductive or family health (n=3) settings. Four themes were identified from the analysis. In "Reasons for What Matters Most," all parents spoke in favor of disclosing to their children and shared their reasons, while clinicians reported the time limitations in clinical settings. In "Managing Emotions, Conflicts, and Needs," a myriad of emotions, including conflict, were entwined in the parents' experiences, and clinicians recognized parents' feelings and needs as well as their own. Within "Desired Content of a Digital Tool," participants provided invaluable feedback on what material and content would be helpful to both parents and clinicians. Participants voiced the design features that would resonate or be useful to them or their patients/clients in "Recommended Design and Usability Features."</p><p><strong>Conclusions: </strong>Findings illustrate the distinct needs and desires of parents-to-be, new parents, and clinicians about providing expanded content for the TELL Tool that is informed by current evidence and end users, ultimately advancing best practices in this area. Future plans include testing the TELL Tool tailored to this additional developmental period o
背景:许多使用捐赠者辅助受孕来组建家庭的父母都很难告诉孩子他们是怎么来的。为了解决这个问题,我们创建了“授权父母告诉和谈论工具”(TELL工具),这是一种针对1至16岁孩子的父母的数字化、心理教育和决策支持干预。最近,我们完成了TELL工具的随机对照试验,显示了可行性、可接受性和前景。然而,在其当前版本中,TELL工具不包括孕妇,孕妇或一岁以下儿童的新父母的内容。目的:本形成性研究的目的是了解孕妇、孕妇和使用供体辅助受孕组建家庭的新父母的观点,以及执业临床医生关于披露的观点,以扩大在美国怀孕和早期生育期间使用TELL工具。方法:采用定性描述方法,采用多方面招聘计划招募20名家长和10名执业临床医生。每个参与者都通过Zoom完成了一次深入的半结构化访谈,该访谈被记录下来,自动转录,检查准确性,随后分析主题。在分析方案中加入了严格的加速数据约简技术。结果:父母包括怀孕(n=6)或新父母(n=15),因为父母一方既怀孕又有一个不到24个月大的孩子。这10名临床医生由一系列多学科卫生保健专业人员组成,分别在生育/不孕症(n=4)、产科和妇女健康(n=3)以及生殖或家庭健康(n=3)部门执业。从分析中确定了四个主题。在“最重要的原因”中,所有的父母都赞成向孩子透露,并分享了他们的原因,而临床医生则报告了临床环境中的时间限制。在《管理情绪、冲突和需求》一书中,包括冲突在内的无数情绪与父母的经历交织在一起,临床医生认识到父母的感受和需求以及他们自己的感受和需求。在“数字工具的期望内容”中,参与者就哪些材料和内容对父母和临床医生都有帮助提供了宝贵的反馈。参与者在“推荐的设计和可用性功能”中表达了对他们或他们的病人/客户产生共鸣或有用的设计功能。结论:研究结果说明了准父母、新父母和临床医生的不同需求和愿望,即根据现有证据和最终用户的信息,为TELL工具提供扩展的内容,最终推进该领域的最佳实践。未来的计划包括测试针对这一额外的怀孕/早期生育发育阶段量身定制的TELL工具。
{"title":"Expanding the Digital, Donor-Assisted Conception Tool to Empower Parental Telling and Talking (TELL Tool) Intervention to the Pregnant and Early Parenthood Periods: Findings From a Qualitative Study.","authors":"Patricia E Hershberger, Kirby Adlam, Mary B Richardson, Alison L Miller, Chelsea Fortin, Martha Driessnack, Harold D Grotevant, Susan C Klock, Lauri A Pasch, Agatha M Gallo","doi":"10.2196/79024","DOIUrl":"10.2196/79024","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;Many parents who use donor-assisted conception to form their families struggle with telling their children about how they came to be. To address this problem, we created the Tool to Empower Parental Telling and Talking (TELL Tool), a digital, psychoeducational, and decision-support intervention for parents with children aged 1 to 16 years. Recently, we completed a pilot randomized controlled trial of the TELL Tool that showed feasibility, acceptability, and promise. However, in its current version, the TELL Tool does not include content for pregnant, expecting, or new parents with children less than 1 year of age.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Objective: &lt;/strong&gt;The aim of this formative study was to understand the views of pregnant, expecting, and new parents who used donor-assisted conception to form their families, along with the views of practicing clinicians about disclosure to expand the TELL Tool for use during the pregnant and early parenthood periods in the United States.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;Using a qualitative descriptive approach, a purposive sample of 20 parents and 10 practicing clinicians was recruited using a multifaceted recruitment plan. Each participant completed an in-depth, semistructured interview over Zoom that was recorded, auto-transcribed, checked for accuracy, and subsequently analyzed for themes. The rigorous and accelerated data reduction technique was incorporated into the analytic plan.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results: &lt;/strong&gt;Parents comprised pregnant (n=6) or new parents (n=15), as one parent was both pregnant and had a child less than 24 months of age. The 10 clinicians, consisting of an array of multidisciplinary health care professionals, were practicing in fertility/infertility (n=4), obstetrics and women's health (n=3), and reproductive or family health (n=3) settings. Four themes were identified from the analysis. In \"Reasons for What Matters Most,\" all parents spoke in favor of disclosing to their children and shared their reasons, while clinicians reported the time limitations in clinical settings. In \"Managing Emotions, Conflicts, and Needs,\" a myriad of emotions, including conflict, were entwined in the parents' experiences, and clinicians recognized parents' feelings and needs as well as their own. Within \"Desired Content of a Digital Tool,\" participants provided invaluable feedback on what material and content would be helpful to both parents and clinicians. Participants voiced the design features that would resonate or be useful to them or their patients/clients in \"Recommended Design and Usability Features.\"&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions: &lt;/strong&gt;Findings illustrate the distinct needs and desires of parents-to-be, new parents, and clinicians about providing expanded content for the TELL Tool that is informed by current evidence and end users, ultimately advancing best practices in this area. Future plans include testing the TELL Tool tailored to this additional developmental period o","PeriodicalId":14841,"journal":{"name":"JMIR Formative Research","volume":"10 ","pages":"e79024"},"PeriodicalIF":2.0,"publicationDate":"2026-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12798919/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145966276","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
Exploring the Acceptability, Appropriateness, and Utility of a Digital Single-Session Intervention (Project SOLVE-NZ) for Adolescent Mental Health in New Zealand: Interview Study Among Students and Teachers. 探索数字单次干预(项目SOLVE-NZ)对新西兰青少年心理健康的可接受性、适当性和效用:对学生和教师的访谈研究。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-01-13 DOI: 10.2196/81259
Morgan Taylor Blind, Nicola Starkey, Amy Bird, Hoana McMillan
<p><strong>Background: </strong>Globally, we face a significant treatment gap in mental health care, with extensive wait times, exorbitant prices, and concerns about appropriateness for non-Western clients. Digital single-session interventions (SSIs) may offer a promising alternative. SSIs target particular mechanisms that underlie broad-ranging psychopathology, including deficits in problem-solving skills.</p><p><strong>Objective: </strong>Developed in the United States, Project SOLVE is a digital SSI that teaches problem-solving skills to adolescents. This study evaluated the acceptability, appropriateness, and utility of an adapted version, Project SOLVE-NZ, among rangatahi (young people) in Aotearoa New Zealand. Additionally, we evaluated a comparable online activity, Project Success-NZ, as a potential active control condition in a future randomized controlled trial of Project SOLVE-NZ.</p><p><strong>Methods: </strong>A sample of school students and teachers completed Project SOLVE-NZ and Project Success-NZ. Feedback on the interventions was collected through focus groups and semistructured interviews. Interviews were recorded, transcribed, and analyzed using reflexive thematic analysis.</p><p><strong>Results: </strong>In total, 12 students (aged between 13 and 14 years; female students: n=6, 50%) participated in a focus group, and 8 teachers (teaching experience: mean 8.75, SD 7.96 years; female teachers: n=5, 62.5%) participated in individual interviews. Participants endorsed the sociocultural relevance of Project SOLVE-NZ and Project Success-NZ to rangatahi in Aotearoa New Zealand and viewed all existing adaptations favorably. Participants felt that the interventions would be valuable to a wide range of rangatahi, helping to fill gaps in students' learning and providing benefits to mental health. Participants also believed that the interventions may be particularly relevant for youths experiencing economic hardship. Interestingly, most participants had no preference for either Project SOLVE-NZ or Project Success-NZ, and they believed that both interventions could provide ongoing support to rangatahi throughout the school year. Teachers provided some suggestions on increasing student engagement with the interventions, namely, through increased cultural and gender representation, visual and literacy aids, whakawhanaungatanga (relationship building), and teacher guidance. Overall, interviews revealed that both interventions were perceived as acceptable, appropriate, and useful for rangatahi in New Zealand and highlighted further adaptations that could be made prior to a randomized controlled trial of Project SOLVE-NZ across schools nationwide.</p><p><strong>Conclusions: </strong>Digital SSIs show promise in addressing the mental health treatment gap for adolescents. Both Project SOLVE-NZ and Project Success-NZ were well-received by students and teachers in Aotearoa New Zealand and may provide benefits to youth mental health. We make the follo
背景:在全球范围内,我们在精神卫生保健方面面临着巨大的治疗差距,包括漫长的等待时间、高昂的价格,以及对非西方客户是否合适的担忧。数字单次会话干预(ssi)可能提供一个有希望的替代方案。ssi针对的是广泛的精神病理背后的特定机制,包括解决问题能力的缺陷。目的:在美国开发的SOLVE项目是一个向青少年传授解决问题技能的数字SSI。本研究评估了一个改编版本Project SOLVE-NZ的可接受性、适当性和实用性,该版本在新西兰奥特罗阿的rangatahi(年轻人)中使用。此外,我们评估了一个类似的在线活动,项目成功-新西兰,作为一个潜在的主动控制条件,在未来的随机对照试验项目解决-新西兰。方法:对完成SOLVE-NZ项目和Success-NZ项目的学生和教师进行抽样调查。通过焦点小组和半结构化访谈收集有关干预措施的反馈。访谈记录,转录,并使用反身性主题分析进行分析。结果:共有12名学生(13 ~ 14岁,女学生6名,占50%)参加了焦点小组,8名教师(教学经验:平均8.75年,标准差7.96年,女教师5名,占62.5%)参加了个别访谈。与会者赞同“解决项目-新西兰”和“成功项目-新西兰”在新西兰奥特罗阿的社会文化相关性,并对所有现有的适应都持积极态度。与会者认为,这些干预措施对各种各样的rangatahi都很有价值,有助于填补学生学习方面的空白,并有利于心理健康。与会者亦认为,这些干预措施对经济困难的青年尤其重要。有趣的是,大多数参与者对“解决计划”和“成功计划”都没有偏好,他们认为这两种干预措施都可以在整个学年中为rangatahi提供持续的支持。教师们提供了一些关于提高学生参与干预的建议,即通过增加文化和性别代表性、视觉和识字辅助、whakawhanaungatanga(建立关系)和教师指导。总的来说,访谈显示,这两种干预措施对于新西兰的rangatahi来说都是可以接受的、适当的和有用的,并强调了在全国学校随机对照试验Project SOLVE-NZ之前可以做出进一步的调整。结论:数字ssi有望解决青少年心理健康治疗缺口。Project SOLVE-NZ和Project Success-NZ都受到新西兰奥特罗阿学生和教师的好评,可能对青少年的心理健康有益。我们对其他有意为年轻人设计数字ssi或类似工具的人提出以下建议:让rangatahi和相关利益相关者参与设计过程,考虑如何实施干预,确保干预适应一系列认知能力,并确保干预反映当今rangatahi的多样性。
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引用次数: 0
Developing a Customizable Texting Intervention for Diabetes Self-Management: Participatory Design Approach. 开发可定制的短信干预糖尿病自我管理:参与式设计方法。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-01-13 DOI: 10.2196/83144
Stephanie A Robinson, Popy Shell, Linda Am, Courtney L Bilodeau, Howard S Gordon, Constance R Uphold, Varsha G Vimalananda, Sarah L Cutrona, Timothy P Hogan, Bridget Smith, Stephanie L Shimada

Background: Uncontrolled diabetes contributes to serious comorbidities and mortality. Effective self-management can improve outcomes, though barriers such as limited education and support often prevent patients from engaging in such behaviors. Automated texting systems show promise to deliver diabetes self-management education as they are accessible and scalable. Furthermore, customizing these systems may further enhance patient engagement compared to standard, one-size-fits-all approaches. However, such customization is more resource-intensive, and it remains unclear whether the added effort meaningfully enhances diabetes self-management and outcomes.

Objective: This study aimed to describe the development of 2 versions of an automated texting system intervention for diabetes self-management: (1) a standard, education-only intervention (Diabetes Self-Management Support; DSMS) and (2) an interactive, customizable intervention (Diabetes Self-Management Support + Interactive and Customizable Messages; DSMS+).

Methods: Two versions of an automated texting system intervention were developed using a participatory design approach that incorporated input from veterans and expert clinicians. Message content was refined through feedback from a multidisciplinary team, veteran coinvestigators, national surveys, interviews, clinical expert panel reviews, and beta testing. Surveys were mailed to 1000 potential participants, oversampling rural, low-income, minority, and female participants. Respondents rated message relevance and provided preferences for content, timing, and frequency. Interviews provided customization preferences. A clinical expert panel reviewed all messages for safety and appropriateness. Beta testing informed final refinements.

Results: Ninety-two surveys were completed (9.2% response rate). Respondents rated 62% of the messages as personally relevant and 61% confidence-enhancing. Interviews with 23 respondents revealed a preference for 1-2 texts per day, emphasizing topics such as healthy eating and weight management. The clinical expert panel reviewed 536 messages, flagging 81 for revision. Beta testing confirmed feasibility and informed refinements to clarity and timing. The 2 resulting interventions were built in the US Department of Veterans Affairs' automated texting system, Annie.

Conclusions: Two text messaging interventions, DSMS and DSMS+, were developed to support diabetes self-management among US veterans. DSMS delivers standard educational content, while DSMS+ incorporates interactive features and personalization. The subsequent clinical trial will assess whether customization enhances engagement and improves diabetes outcomes, providing insights into the potential of tailored mobile health interventions for chronic disease management.

背景:未控制的糖尿病会导致严重的合并症和死亡率。有效的自我管理可以改善结果,尽管诸如有限的教育和支持等障碍通常会阻止患者参与此类行为。自动短信系统由于易于使用和可扩展,有望提供糖尿病自我管理教育。此外,与标准的、一刀切的方法相比,定制这些系统可以进一步提高患者的参与度。然而,这种定制需要更多的资源,目前尚不清楚额外的努力是否有意义地提高了糖尿病的自我管理和结果。目的:本研究旨在描述糖尿病自我管理自动短信系统干预的两个版本的开发:(1)标准的,仅教育的干预(糖尿病自我管理支持;DSMS)和(2)交互式的,可定制的干预(糖尿病自我管理支持+交互式和可定制的消息;DSMS+)。方法:采用参与式设计方法开发了两个版本的自动短信系统干预,其中包括退伍军人和专家临床医生的输入。信息内容通过来自多学科团队、资深合作研究者、国家调查、访谈、临床专家小组评论和beta测试的反馈进行完善。调查问卷邮寄给1000名潜在参与者,对农村、低收入、少数民族和女性参与者进行了抽样调查。受访者对信息的相关性进行评级,并提供对内容、时间和频率的偏好。访谈提供了定制偏好。临床专家小组审查了所有信息的安全性和适当性。Beta测试通知了最终的改进。结果:共完成92项调查,回复率为9.2%。受访者认为62%的信息与个人相关,61%的信息增强了信心。对23名受访者的采访显示,他们更喜欢每天发1-2条短信,强调健康饮食和体重管理等话题。临床专家小组审查了536条信息,其中81条需要修改。Beta测试确认了可行性,并告知了清晰度和时间的改进。由此产生的两个干预是在美国退伍军人事务部的自动短信系统Annie中建立的。结论:开发了两种短信干预措施,DSMS和DSMS+,以支持美国退伍军人糖尿病自我管理。DSMS提供标准的教育内容,而DSMS+结合了互动功能和个性化。随后的临床试验将评估定制化是否能提高参与度并改善糖尿病结局,从而深入了解定制化移动健康干预慢性病管理的潜力。
{"title":"Developing a Customizable Texting Intervention for Diabetes Self-Management: Participatory Design Approach.","authors":"Stephanie A Robinson, Popy Shell, Linda Am, Courtney L Bilodeau, Howard S Gordon, Constance R Uphold, Varsha G Vimalananda, Sarah L Cutrona, Timothy P Hogan, Bridget Smith, Stephanie L Shimada","doi":"10.2196/83144","DOIUrl":"10.2196/83144","url":null,"abstract":"<p><strong>Background: </strong>Uncontrolled diabetes contributes to serious comorbidities and mortality. Effective self-management can improve outcomes, though barriers such as limited education and support often prevent patients from engaging in such behaviors. Automated texting systems show promise to deliver diabetes self-management education as they are accessible and scalable. Furthermore, customizing these systems may further enhance patient engagement compared to standard, one-size-fits-all approaches. However, such customization is more resource-intensive, and it remains unclear whether the added effort meaningfully enhances diabetes self-management and outcomes.</p><p><strong>Objective: </strong>This study aimed to describe the development of 2 versions of an automated texting system intervention for diabetes self-management: (1) a standard, education-only intervention (Diabetes Self-Management Support; DSMS) and (2) an interactive, customizable intervention (Diabetes Self-Management Support + Interactive and Customizable Messages; DSMS+).</p><p><strong>Methods: </strong>Two versions of an automated texting system intervention were developed using a participatory design approach that incorporated input from veterans and expert clinicians. Message content was refined through feedback from a multidisciplinary team, veteran coinvestigators, national surveys, interviews, clinical expert panel reviews, and beta testing. Surveys were mailed to 1000 potential participants, oversampling rural, low-income, minority, and female participants. Respondents rated message relevance and provided preferences for content, timing, and frequency. Interviews provided customization preferences. A clinical expert panel reviewed all messages for safety and appropriateness. Beta testing informed final refinements.</p><p><strong>Results: </strong>Ninety-two surveys were completed (9.2% response rate). Respondents rated 62% of the messages as personally relevant and 61% confidence-enhancing. Interviews with 23 respondents revealed a preference for 1-2 texts per day, emphasizing topics such as healthy eating and weight management. The clinical expert panel reviewed 536 messages, flagging 81 for revision. Beta testing confirmed feasibility and informed refinements to clarity and timing. The 2 resulting interventions were built in the US Department of Veterans Affairs' automated texting system, Annie.</p><p><strong>Conclusions: </strong>Two text messaging interventions, DSMS and DSMS+, were developed to support diabetes self-management among US veterans. DSMS delivers standard educational content, while DSMS+ incorporates interactive features and personalization. The subsequent clinical trial will assess whether customization enhances engagement and improves diabetes outcomes, providing insights into the potential of tailored mobile health interventions for chronic disease management.</p>","PeriodicalId":14841,"journal":{"name":"JMIR Formative Research","volume":"10 ","pages":"e83144"},"PeriodicalIF":2.0,"publicationDate":"2026-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12848483/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145959483","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
Acceptability of and Implementation Supports for Video Directly Observed Treatment to Enhance Methadone Dosing Flexibility in a Multisite Opioid Treatment Program: Qualitative Rapid Needs Assessment Study. 视频直接观察治疗在多地点阿片类药物治疗项目中增强美沙酮给药灵活性的可接受性和实施支持:定性快速需求评估研究
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-01-12 DOI: 10.2196/84162
Judith I Tsui, Elizabeth J Austin, Julia A Dunn, Alexander J Gojic, Elenore P Bhatraju, James Darnton, Paul Grekin, Sean Soth, Steve Woolworth, Emily C Williams, Kevin A Hallgren

Background: Methadone is a first-line treatment for opioid use disorder, which is delivered in federally regulated opioid treatment programs (OTPs). Federal policies require directly observed dosing of methadone followed by graduated provision of nonobserved doses to take at home (ie, "take-home" dosing) after demonstrated stability is achieved. Policy changes since the COVID-19 pandemic have greatly expanded take-home dosing. Video directly observed treatment (video DOT) is an approach in which patients submit videos of themselves taking medications, which are asynchronously reviewed to verify adherence.

Objective: In preparation for an implementation trial evaluating the adoption of video DOT in OTP settings, we conducted a rapid needs assessment with multidisciplinary stakeholders to assess acceptability, perceived benefits, and needed support for video DOT to monitor take-home methadone dosing.

Methods: In our rapid needs assessment, we explored perspectives of multidisciplinary stakeholders (N=20) at 3 clinical sites within a single OTP in western Washington state. Trained qualitative researchers took ethnographic field notes during meetings with organizational leadership and in-person site visits with clinical and administrative staff. Field notes were analyzed via a team-based rapid assessment process using coding templates informed by the Consolidated Framework for Implementation Research. Summaries of qualitative data were iteratively reviewed by the study team and further confirmed with site stakeholders.

Results: Stakeholders included leadership (n=6, 30%), medical providers (n=4, 20%), substance use disorder counselors (n=7, 35%), and clinic managers and support staff (n=3, 15%). Stakeholders perceived that video DOT could lessen the barriers patients face, including travel burden (eg, time and cost) and stigma. They also identified that video DOT could have important impacts on early care retention, given expansions of take-home dosing. However, stakeholders anticipated an added burden for clinical staff and emphasized the need for implementation supports that would limit burden, such as additional staff support for video submission review and clear communication pathways when video submissions require additional clinical input.

Conclusions: A rapid needs assessment of OTP sites for a future implementation study suggested that stakeholders saw potential benefits for patients receiving video DOT, but there were concerns that this would add to their work burden. Learnings informed the subsequent tailoring of clinical use cases and implementation supports.

背景:美沙酮是阿片类药物使用障碍的一线治疗方法,在联邦监管的阿片类药物治疗计划(OTPs)中提供。联邦政策要求美沙酮的直接观察剂量,然后在达到证明的稳定性后,逐步提供在家服用的非观察剂量(即“带回家”剂量)。自COVID-19大流行以来的政策变化大大扩大了带回家的剂量。视频直接观察治疗(Video direct observed treatment,简称Video DOT)是一种患者提交自己服药的视频的方法,这些视频会被异步审查以验证依从性。目的:为了准备一项评估视频DOT在OTP环境中采用的实施试验,我们与多学科利益相关者进行了快速需求评估,以评估视频DOT监测美沙酮带回家剂量的可接受性、感知效益和所需支持。方法:在我们的快速需求评估中,我们在华盛顿州西部一个OTP的3个临床站点探索了多学科利益相关者(N=20)的观点。训练有素的定性研究人员在与组织领导的会议和与临床和行政人员的实地考察中记录了民族志实地笔记。实地记录通过基于团队的快速评估过程进行分析,使用由实施研究综合框架提供的编码模板。研究小组反复审查定性数据的摘要,并与现场利益相关者进一步确认。结果:利益相关者包括领导(n=6, 30%)、医疗提供者(n=4, 20%)、物质使用障碍咨询师(n=7, 35%)和诊所管理人员和支持人员(n=3, 15%)。利益相关者认为视频DOT可以减少患者面临的障碍,包括旅行负担(如时间和费用)和耻辱。他们还发现,鉴于带回家剂量的扩大,视频DOT可能对早期护理的保留产生重要影响。然而,利益攸关方预计临床工作人员的负担会增加,并强调需要实施支持,以限制负担,例如,在视频提交需要额外临床投入时,为视频提交审查提供额外的工作人员支持,并明确沟通途径。结论:对未来实施研究的OTP站点的快速需求评估表明,利益相关者看到了接受视频DOT的患者的潜在利益,但也有人担心这会增加他们的工作负担。学习为后续的临床用例裁剪和实现支持提供了信息。
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引用次数: 0
Evaluating Spanish Translations of Emergency Department Discharge Instructions by a Large Language Model: Tool Validation and Reliability Study. 用大语言模型评估急诊科出院指示的西班牙语翻译:工具验证和可靠性研究。
IF 2 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-01-12 DOI: 10.2196/79676
Jossie A Carreras Tartak, Ryan Cl Brewster, Daniela Arango Isaza, Antonio Berumen Martinez, Ana Grafals, Phanidhar Adusumilli, Ted Fitzgerald, Roger Orcutt, Larry A Nathanson, Adrian D Haimovich

When given a sample of 100 emergency department discharge instructions, Claude Sonnet, a large language model, produced accurate Spanish translations as evaluated by Spanish-speaking physicians and medical interpreters.

当提供100份急诊科出院说明的样本时,Claude Sonnet,一个大型语言模型,根据讲西班牙语的医生和医疗口译员的评估,产生了准确的西班牙语翻译。
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引用次数: 0
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