Evaluating and Optimizing Just-in-Time Adaptive Interventions in a Digital Mental Health Intervention (Wysa for Chronic Pain) for Middle-Aged and Older Adults With Chronic Pain: Protocol for a Series of Randomized Trials.

IF 1.5 Q3 HEALTH CARE SCIENCES & SERVICES
Abby L Cheng, Joanna Abraham, Sarah M Hartz, Eric B Laber, J Philip Miller
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引用次数: 0

Abstract

Background: On a population level, digital mental health interventions effectively reduce depression and anxiety symptoms. However, middle-aged and older adults with chronic pain and coexisting depression or anxiety have not been adequately represented in digital mental health studies.

Objective: The goal of this study is to refine an existing mobile, digital mental health intervention (Wysa for Chronic Pain) that addresses symptoms of depression, anxiety, and coexisting chronic pain for the unique challenges and technology use patterns of middle-aged and older adults.

Methods: Using a mixed methods, human-centered design approach and a series of randomized trials, we will test and iteratively refine just-in-time adaptive interventions (JITAIs) that are designed to increase engagement with a digital mental health intervention. Participants will be aged 45 years or older, endorse at least moderately severe depression or anxiety symptoms (Patient Health Questionnaire-9 or Generalized Anxiety Disorder-7 score ≥10), and have coexisting chronic pain (ie, pain on most days or every day in the past 3 months), and live in the United States. In this open, web-based trial, participants will all receive Wysa for Chronic Pain (by Wysa), which uses a behavioral activation framework and encourages users to work toward pain acceptance. The fully automated intervention also includes cognitive behavioral therapy, mindfulness, and sleep tools, among others. In each trial, participants will be randomized during a maximum 12-week study period to receive versus not receive novel JITAIs that are intended to reduce navigation burden and improve usability (and subsequent engagement and clinical effectiveness). The JITAIs are being designed with iterative user feedback, guided by the Discover, Design/Build, and Test framework and the Behavioral Intervention Technology model. The proximal outcome for each JITAI is related to engagement with Wysa for Chronic Pain after JITAI delivery (compared to when no JITAI is delivered). The primary distal clinical outcome is the Patient Health Questionnaire Anxiety and Depression Scale. Based on statistical analysis that is triangulated with qualitative feedback from a subsample of trial participants, the JITAIs will be iteratively refined and retested in subsequent microrandomized trials until retesting of refined adaptations no longer yields meaningful improvement in immediate engagement or a maximum of 5 total trials have been completed.

Results: Institutional review board approval was obtained on April 11, 2025. The first participant was enrolled on June 2, 2025, and recruitment is expected to conclude in 2026.

Conclusions: Completion of this project will result in iteratively refined JITAIs that are designed to improve usability and engagement with a digital mental health intervention by middle-aged and older adults with depression or anxiety and coexisting chronic pain.

Trial registration: ClinicalTrials.gov NCT06978166; https://clinicaltrials.gov/study/NCT06978166.

International registered report identifier (irrid): PRR1-10.2196/77532.

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评估和优化针对中老年人慢性疼痛的数字心理健康干预(Wysa for Chronic Pain)中的即时适应性干预:一系列随机试验方案
背景:在人群水平上,数字心理健康干预有效地减少了抑郁和焦虑症状。然而,在数字心理健康研究中,患有慢性疼痛和共存抑郁或焦虑的中老年人并没有得到充分的代表。目的:本研究的目的是改进现有的移动、数字心理健康干预(Wysa for Chronic Pain),针对中老年人的独特挑战和技术使用模式,解决抑郁、焦虑和共存的慢性疼痛症状。方法:采用混合方法、以人为本的设计方法和一系列随机试验,我们将测试并迭代改进旨在增加数字心理健康干预的即时适应性干预(JITAIs)。参与者年龄在45岁或以上,至少有中度重度抑郁或焦虑症状(患者健康问卷-9或广泛性焦虑障碍-7评分≥10),并伴有慢性疼痛(即在过去3个月内大部分时间或每天疼痛),并且居住在美国。在这个开放的、基于网络的试验中,所有参与者都将接受Wysa治疗慢性疼痛(由Wysa公司开发),它使用行为激活框架,鼓励用户努力接受疼痛。全自动干预还包括认知行为疗法、正念和睡眠工具等。在每项试验中,参与者将在最长12周的研究期间随机接受或不接受新型jitai,旨在减少导航负担并提高可用性(以及随后的参与度和临床有效性)。jitai是在发现、设计/构建和测试框架以及行为干预技术模型的指导下,根据迭代用户反馈进行设计的。每个JITAI的近端结果与JITAI交付后使用Wysa治疗慢性疼痛有关(与未交付JITAI时相比)。主要的远端临床结果是患者健康问卷焦虑和抑郁量表。基于统计分析和来自试验参与者子样本的定性反馈,jitai将在随后的微随机试验中反复改进和重新测试,直到改进的适应性重新测试不再产生即时参与的有意义的改善或最多完成5个试验。结果:于2025年4月11日获得机构审查委员会批准。第一名参与者于2025年6月2日招募,预计招募将于2026年结束。结论:该项目的完成将产生迭代改进的jitai,旨在提高患有抑郁或焦虑并并存慢性疼痛的中老年成年人的可用性和参与数字心理健康干预。试验注册:ClinicalTrials.gov NCT06978166;https://clinicaltrials.gov/study/NCT06978166.International注册报告标识符(irrid): PRR1-10.2196/77532。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.40
自引率
5.90%
发文量
414
审稿时长
12 weeks
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