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评估一款基于处方的针对恐慌症患者的移动应用程序及其临床医生管理控制台的可用性:对照用户研究。

Assessing the Usability of a Prescription-Based Mobile App for Patients With Panic Disorder and Its Management Console for Clinicians: Controlled User Study.

作者信息

Ko Yujin, Lee Jeemin, Ham Kyunghee, Cho Yesol, Shin Yu-Bin, Min Choongki, Kim Kyungnam, Jang Wonseuk, Jung Hayeon, Kim Jae-Jin

机构信息

Institute of Behavioral Sciences in Medicine, Yonsei University College of Medicine, Seoul, Republic of Korea.

Department of Psychiatry, Soonchunhyang University Bucheon Hospital, Bucheon, Republic of Korea.

出版信息

JMIR Form Res. 2025 Oct 17;9:e76843. doi: 10.2196/76843.

Abstract

BACKGROUND

Panic disorder is characterized by sudden panic attacks and persistent anticipatory anxiety. While pharmacotherapy remains effective, patients with panic disorder often experience residual symptoms and functional impairments. Lifestyle factors influence symptom severity but are often unaddressed in routine psychiatric care. Most current digital therapeutics for panic disorder have a limited scope, lack integration with clinicians, and fail to consider behavioral patterns. To address these limitations, our research team developed a prescription-based app that supports structured cognitive behavioral therapy practice, real-life symptom management, and lifestyle modifications for patients with panic disorder, and a management console-a web-based platform that allows clinicians to monitor the patients' engagement and progress as well as determine therapeutic options if necessary.

OBJECTIVE

This study aimed to test the usability of the app and management console by evaluating their interface, functionality, and user experience. The primary goal was to identify the strengths and areas for further improvement of these software devices and to develop a list of modifications to improve the user experience and clinical applicability in updates to refine the devices for a future clinical trial.

METHODS

Usability data were collected by investigators at a medical device usability research center without the involvement of the development research team, and the participants were 15 patients with panic disorder and 15 psychiatrists. Each group completed experimental use of the app or management console and scored the convenience and safety of its modules, questionnaire evaluations for the acceptability, and presentation of verbal subjective feedback on areas for improvement. Based on the participants' suggestions, a list of items that need to be modified to improve functionality and ease of use for each device was created.

RESULTS

Patients completed 155 assigned tasks for the app with more than 98% success, and psychiatrists completed 34 tasks for the management console with more than 86% success. The convenience and safety scores for the app and management console exceeded the neutral threshold (mean >4.5). For all statements about the acceptability, both patients and psychiatrists responded at the level of agreeing with a score exceeding 3 (mean: 3.64.3 and 44.7, respectively). There were 38 suggestions for app improvements and 66 suggestions for management console improvements, most of which were incorporated in the modification list.

CONCLUSIONS

Patients reported that the app might be easy to use and help manage anxiety, and psychiatrists found the management console practical and well-suited for outpatients. By combining patient-facing therapeutic tools with clinician-driven prescription and monitoring, the devices offer a solution aligned with clinically integrated, real-world psychiatric care. Modified devices based on the improvement suggestions presented in this study will be evaluated in future clinical trials for their impact on engagement and treatment outcomes.

摘要

背景

惊恐障碍的特征是突发惊恐发作和持续性预期焦虑。虽然药物治疗仍然有效,但惊恐障碍患者常出现残留症状和功能损害。生活方式因素会影响症状严重程度,但在常规精神科护理中往往未得到解决。目前大多数针对惊恐障碍的数字疗法范围有限,缺乏与临床医生的整合,且未考虑行为模式。为解决这些局限性,我们的研究团队开发了一款基于处方的应用程序,为惊恐障碍患者提供结构化认知行为疗法实践、现实生活中的症状管理和生活方式调整支持,以及一个管理控制台——一个基于网络的平台,使临床医生能够监测患者的参与情况和进展,并在必要时确定治疗方案。

目的

本研究旨在通过评估应用程序和管理控制台的界面、功能和用户体验来测试其可用性。主要目标是确定这些软件设备的优势和需要进一步改进的方面,并制定一份修改清单,以改善用户体验和临床适用性,以便在更新中完善这些设备,用于未来的临床试验。

方法

可用性数据由医疗器械可用性研究中心的研究人员收集,开发研究团队未参与,参与者为15名惊恐障碍患者和15名精神科医生。每组完成应用程序或管理控制台的实验使用,并对其模块的便利性和安全性进行评分,对可接受性进行问卷调查,并就改进领域提供口头主观反馈。根据参与者的建议,创建了一份需要修改的项目清单,以提高每个设备的功能和易用性。

结果

患者完成了应用程序分配的155项任务,成功率超过98%,精神科医生完成了管理控制台的34项任务,成功率超过86%。应用程序和管理控制台的便利性和安全性评分超过中性阈值(平均值>4.5)。对于所有关于可接受性的陈述,患者和精神科医生的回答均为同意程度,得分超过3分(平均值分别为3.64.3和44.7)。有38条应用程序改进建议和66条管理控制台改进建议,其中大部分已纳入修改清单。

结论

患者报告称该应用程序可能易于使用并有助于管理焦虑,精神科医生发现管理控制台实用且非常适合门诊患者。通过将面向患者的治疗工具与临床医生驱动的处方和监测相结合,这些设备提供了一种与临床综合、现实世界精神科护理相一致的解决方案。基于本研究提出的改进建议修改后的设备将在未来的临床试验中评估其对参与度和治疗结果的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/710e/12533929/a39c5ab8d46c/formative-v9-e76843-g001.jpg

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