Kaiser Permanente Washington Health Research Institute, Seattle, WA, United States.
Department of Health Systems and Population Health, School of Public Health, University of Washington, Seattle, WA, United States.
JMIR Form Res. 2024 Sep 2;8:e59088. doi: 10.2196/59088.
Delivering prescription digital therapeutics (ie, evidence-based interventions designed to treat, manage, or prevent disorders via websites or smartphone apps) in primary care could increase patient access to substance use disorder (SUD) treatments. However, the optimal approach to implementing prescription digital therapeutics in primary care remains unknown.
This pilot study is a precursor to a larger trial designed to test whether implementation strategies (practice facilitation [PF] and health coaching [HC]) improve the delivery of prescription digital therapeutics for SUDs in primary care. This mixed methods study describes outcomes among patients in the 2 pilot clinics and presents qualitative findings on implementation.
From February 10 to August 6, 2021, a total of 3 mental health specialists embedded in 2 primary care practices of the same integrated health system were tasked with offering app-based prescription digital therapeutics to patients with SUD. In the first half of the pilot, implementation activities included training and supportive tools. PF (at 1 clinic) and HC (at 2 clinics) were added in the second half. All study analyses relied on secondary data, including electronic health records and digital therapeutic vendor data. Primary outcomes were the proportion of patients reached by the prescription digital therapeutics and fidelity related to ideal use. We used qualitative methods to assess the adherence to planned activities and the barriers and facilitators to implementing prescription digital therapeutics.
Of all 18 patients prescribed the apps, 10 (56%) downloaded the app and activated their prescription, and 8 (44%) completed at least 1 module of content. Patients who activated the app completed 1 module per week on average. Ideal use (fidelity) was defined as completing 4 modules per week and having a monthly SUD-related visit; 1 (6%) patient met these criteria for 10 weeks (of the 12-week prescription period). A total of 5 (28%) patients had prescriptions while HC was available, 2 (11%) were successfully contacted, and both declined coaching. Clinicians reported competing clinical priorities, technical challenges, and logistically complex workflows in part because the apps required a prescription. Some pilot activities were impacted by staff turnover that coincided with the COVID-19 pandemic. The facilitators to implementation were high engagement and the perception that the apps could meet patient needs.
The pilot study encountered the barriers to implementing prescription digital therapeutics in a real-world primary care setting, especially staffing shortages, turnover, and competing priorities for clinic teams. The larger randomized trial will clarify the extent to which PF and HC improve the implementation of digital therapeutics.
ClinicalTrials.gov NCT04907045; https://clinicaltrials.gov/study/NCT04907045.
在初级保健中提供处方数字疗法(即,旨在通过网站或智能手机应用程序治疗、管理或预防疾病的基于证据的干预措施)可以增加患者获得物质使用障碍(SUD)治疗的机会。然而,在初级保健中实施处方数字疗法的最佳方法仍不清楚。
这项试点研究是一项更大规模试验的前奏,旨在测试实施策略(实践促进[PF]和健康教练[HC])是否可以提高初级保健中 SUD 处方数字疗法的提供。这项混合方法研究描述了两个试点诊所中患者的结果,并介绍了实施方面的定性发现。
从 2021 年 2 月 10 日至 8 月 6 日,总共 3 名心理健康专家被嵌入同一综合卫生系统的 2 个初级保健实践中,负责向 SUD 患者提供基于应用程序的处方数字疗法。在试点的前半段,实施活动包括培训和支持工具。在下半年增加了 PF(在一个诊所)和 HC(在两个诊所)。所有研究分析都依赖于二次数据,包括电子健康记录和数字治疗供应商数据。主要结果是通过处方数字疗法接触到的患者比例和与理想使用相关的保真度。我们使用定性方法评估了计划活动的遵守情况以及实施处方数字疗法的障碍和促进因素。
在所有 18 名被开出应用程序的患者中,有 10 名(56%)下载了应用程序并激活了他们的处方,有 8 名(44%)完成了至少 1 个模块的内容。激活应用程序的患者平均每周完成 1 个模块。理想使用(保真度)被定义为每周完成 4 个模块并进行每月一次的 SUD 相关就诊;有 1 名(6%)患者在 12 周的处方期内满足了这 10 周的标准。有 5 名(28%)患者在 HC 可用时开了处方,有 2 名(11%)成功联系上了,但都拒绝了辅导。临床医生报告说存在竞争激烈的临床优先事项、技术挑战和物流复杂的工作流程,部分原因是这些应用程序需要处方。一些试点活动受到员工流动的影响,恰逢 COVID-19 大流行。实施的促进因素是高参与度和认为应用程序可以满足患者需求的观念。
试点研究遇到了在现实世界中的初级保健环境中实施处方数字疗法的障碍,特别是人手短缺、人员流动和诊所团队的竞争优先事项。更大规模的随机试验将阐明 PF 和 HC 在多大程度上提高了数字治疗的实施。
ClinicalTrials.gov NCT04907045; https://clinicaltrials.gov/study/NCT04907045。