eHealth/mHealth/digital health

  • 文章类型: Journal Article
    目的:移动健康(mHealth)干预措施可能是促进儿科人群健康行为的有效策略,但是他们在实施阶段的成功被证明具有挑战性。本文的目的是提供使用以人为中心的设计(HCD)方法以最大程度地发挥实施潜力的蓝图,通过分享一个年轻人的例子-,家庭-,和临床医生参与创建旨在促进医疗保健过渡准备的mHealth干预措施的过程。
    方法:遵循与三个咨询委员会合作的HCD方法,我们分两个阶段对13~15岁的患者及其护理人员进行了半结构化访谈.在第一阶段,参与者描述了过渡过程中的挑战,并产生了关于格式的想法,内容,以及mHealth工具的其他品质。对于第二阶段,早期青少年和护理人员提供了两个顺序干预原型的迭代反馈。使用第一阶段的专题分析和第二阶段的快速评估过程对数据进行了分析。
    结果:我们采访了11名青年和8名护理人员。样本包括患有一系列慢性健康状况的青少年。在第一阶段,与会者支持开发自治建设工具的想法,通过社交媒体风格的视频提供过渡准备教育。在第二阶段,参与者对连续的原型做出了积极的回应,并提供了使信息可访问的建议,相关,和参与。
    结论:本文中共享的程序可以告知其他研究人员计划与实施伙伴合作应用HCD以开发mHealth干预措施。我们未来的方向包括迭代开发更多的视频,以促进过渡准备和在临床护理中实施干预。
    OBJECTIVE: Mobile health (mHealth) interventions may be an efficacious strategy for promoting health behaviors among pediatric populations, but their success at the implementation stage has proven challenging. The purpose of this article is to provide a blueprint for using human-centered design (HCD) methods to maximize the potential for implementation, by sharing the example of a youth-, family-, and clinician-engaged process of creating an mHealth intervention aimed at promoting healthcare transition readiness.
    METHODS: Following HCD methods in partnership with three advisory councils, we conducted semistructured interviews with 13- to 15-year-old patients and their caregivers in two phases. In Phase 1, participants described challenges during the transition journey, and generated ideas regarding the format, content, and other qualities of the mHealth tool. For Phase 2, early adolescents and caregivers provided iterative feedback on two sequential intervention prototypes. Data were analyzed using thematic analysis in Phase 1 and the rapid assessment process for Phase 2.
    RESULTS: We interviewed 11 youth and 8 caregivers. The sample included adolescents with a range of chronic health conditions. In Phase 1, participants supported the idea of developing an autonomy-building tool, delivering transition readiness education via social media style videos. In Phase 2, participants responded positively to the successive prototypes and provided suggestions to make information accessible, relatable, and engaging.
    CONCLUSIONS: The procedures shared in this article could inform other researchers\' plans to apply HCD in collaboration with implementation partners to develop mHealth interventions. Our future directions include iteratively developing more videos to promote transition readiness and implementing the intervention in clinical care.
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  • 文章类型: Journal Article
    目标:在美国南部,感染HIV(YLHIV)的青年在整个HIV护理连续过程中结局不佳,并且处于病毒学失败的高风险中。这项研究采用了一种定性的,社区参与的方法,为南卡罗来纳州(SC)的YLHIV量身定制的移动健康(mHealth)工具的开发提供信息。
    方法:对SC(n=16)及其HIV护理提供者(n=15)的YLHIV进行了半结构化定性访谈。还与以艾滋病毒为重点的社区组织工作人员(n=23)进行了焦点小组讨论(FGD)。访谈和FGD查询了为YLHIV量身定制的未来mHealth工具的所需组件。使用基于团队的快速定性方法分析数据。
    结果:所有线人,出现了与艾滋病毒医疗管理相关的关键主题,包括与医疗提供者联系的愿望,预约和用药提醒,和准确的艾滋病毒信息。此外,线人表示希望将心理健康资源整合到应用程序中。与艾滋病毒阳性同龄人的联系也成为青年线人的主要愿望。在APP设计方面,线人强调需要严格的隐私惯例,对年轻人友好的设计,使用补偿,以及与现有医疗保健系统的整合。
    结论:针对YLHIV开发的mHealth干预措施除了满足医疗需求外,还应满足YLHIV的心理健康和社会需求。此外,在设计数字工具时,艾滋病毒的高度污名化性质需要仔细考虑——年轻人希望他们的隐私得到优先考虑,但也表达了对社会支持的强烈愿望,以帮助应对这种慢性健康状况的孤立和耻辱。
    OBJECTIVE: Youth living with HIV (YLHIV) in the southern United States experience poor outcomes across the HIV care continuum and are at high-risk for virologic failure. This study used a qualitative, community-engaged approach to inform the development of a tailored mobile Health (mHealth) tool for YLHIV in South Carolina (SC).
    METHODS: Semistructured qualitative interviews were conducted with YLHIV in SC (n = 16) and their HIV care providers (n = 15). Focus group discussions (FGDs) were also conducted with HIV-focused community-based organization staff (n = 23). Interviews and FGDs queried desired components for a future mHealth tool tailored for YLHIV. Data were analyzed using a team-based rapid qualitative approach.
    RESULTS: Across informants, key themes emerged related to medical management of HIV, including a desire for connections with medical providers, appointment and medication reminders, and accurate HIV information. In addition, informants voiced a desire for mental health resources to be integrated into the app. Connection with HIV-positive peers also emerged as a key desire from youth informants. In terms of app design, informants emphasized the need for strict privacy practices, a youth-friendly design, compensation for use, and integration with existing healthcare systems.
    CONCLUSIONS: mHealth interventions developed for YLHIV should meet the mental health and social needs of YLHIV in addition to their medical needs. In addition, the highly stigmatized nature of HIV requires careful consideration when designing digital tools-youth want their privacy prioritized, but also express strong desire for social support to help cope with the isolation and stigma of this chronic health condition.
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  • 文章类型: Journal Article
    目标:开发一个以患者和家庭为中心的生育相关医疗决策援助(AFFRMED)互动网站,针对跨性别和非二元(TNB)青年/年轻人及其父母,通过以用户为中心的参与式设计,促进有关生育保护干预措施的共享决策。
    方法:招募有兴趣或目前正在接受青春期抑制或性别确认激素治疗的TNB青年/年轻人和符合条件的TNB青年/年轻人的父母参加一系列以人为中心的迭代共同设计会议,以开发初始AFFRMED原型。随后,TNB青年/年轻人和TNB青年/年轻人的父母被招募进行可用性测试面试。涉及可用性的度量(即,在情景调查问卷之后,净预测得分,系统可用性量表)。
    结果:27名参与者完成了18次迭代共同设计会议,并对10个版本的AFFRMED(16名TNB青年/年轻人和11名父母)提供了反馈。9名TNB青年/年轻人和6名父母完成了个人可用性测试访谈。总的来说,参与者对AFFRMED的可接受性评价很高,适当性,可用性,和满意度。然而,得分因治疗队列而异,有兴趣或目前正在接受青春期抑制治疗的TNB青少年报告的可用性得分最低。
    结论:我们共同创建了一个以青年和家庭为中心的生育决策辅助原型,该原型在网上提供教育和决策支持,交互式格式。未来的方向包括测试决策援助在提高生育能力和生育能力保存知识方面的功效,决策自我效能感,和决策满意度。
    OBJECTIVE: To develop a patient- and family-centered Aid For Fertility-Related Medical Decisions (AFFRMED) interactive website targeted for transgender and nonbinary (TNB) youth/young adults and their parents to facilitate shared decision-making about fertility preservation interventions through user-centered participatory design.
    METHODS: TNB youth/young adults interested in or currently receiving pubertal suppression or gender-affirming hormone treatment and parents of eligible TNB youth/young adults were recruited to participate in a series of iterative human-centered co-design sessions to develop an initial AFFRMED prototype. Subsequently, TNB youth/young adults and parents of TNB youth/young adults were recruited for usability testing interviews, involving measures of usability (i.e., After Scenario Questionnaire, Net Promotor Score, System Usability Scale).
    RESULTS: Twenty-seven participants completed 18 iterative co-design sessions and provided feedback on 10 versions of AFFRMED (16 TNB youth/young adults and 11 parents). Nine TNB youth/young adults and six parents completed individual usability testing interviews. Overall, participants rated AFFRMED highly on measures of acceptability, appropriateness, usability, and satisfaction. However, scores varied by treatment cohort, with TNB youth interested in or currently receiving pubertal suppression treatment reporting the lowest usability scores.
    CONCLUSIONS: We co-created a youth- and family-centered fertility decision aid prototype that provides education and decision support in an online, interactive format. Future directions include testing the efficacy of the decision aid in improving fertility and fertility preservation knowledge, decisional self-efficacy, and decision satisfaction.
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