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在PerPAIN随机对照试验中,使用基于监测的反馈和微干预措施,将慢性肌肉骨骼疼痛患者的注意力重新聚焦于积极事件:一项微随机试验方案

Refocusing of Attention on Positive Events Using Monitoring-Based Feedback and Microinterventions for Patients With Chronic Musculoskeletal Pain in the PerPAIN Randomized Controlled Trial: Protocol for a Microrandomized Trial.

作者信息

Ader Leonie, Schick Anita, Löffler Martin, Löffler Annette, Beiner Eva, Eich Wolfgang, Vock Stephanie, Sirazitdinov Andrei, Malone Christopher, Hesser Jürgen, Hopp Michael, Ruckes Christian, Flor Herta, Tesarz Jonas, Reininghaus Ulrich

机构信息

Department of Public Mental Health, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.

Institute of Cognitive and Clinical Neuroscience, Central Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.

出版信息

JMIR Res Protoc. 2023 Sep 20;12:e43376. doi: 10.2196/43376.

DOI:10.2196/43376
PMID:37728983
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10551789/
Abstract

BACKGROUND

Chronic musculoskeletal pain (CMSP) affects between 13% and 47% of the population, with a global growth rate of 20.3% within the last 15 years, suggesting that there is a high need for effective treatments. Pain diaries have long been a common tool in nonpharmacological pain treatment for monitoring and providing feedback on patients' symptoms in daily life. More recently, positive refocusing techniques have come to be used, promoting pain-free episodes and positive outcomes rather than focusing on managing the pain.

OBJECTIVE

This study aims to evaluate the feasibility (ie, acceptability, intervention adherence, and fidelity) and initial signals of efficacy of the PerPAIN app, an ecological momentary intervention for patients with CMSP. The app comprises digitalized monitoring using the experience sampling method (ESM) and feedback. In addition, the patients receive 3 microinterventions targeted at refocusing of attention on positive events.

METHODS

In a microrandomized trial, we will recruit 35 patients with CMSP who will be offered the app for 12 weeks. Participants will be prompted to fill out 4 ESM monitoring questionnaires a day assessing information on their current context and the proximal outcome variables: absence of pain, positive mood, and subjective activity. Participants will be randomized daily and weekly to receive no feedback, verbal feedback, or visual feedback on proximal outcomes assessed by the ESM. In addition, the app will encourage participants to complete 3 microinterventions based on positive psychology and cognitive behavioral therapy techniques. These microinterventions are prompts to report joyful moments and everyday successes or to plan pleasant activities. After familiarizing themselves with each microintervention individually, participants will be randomized daily to receive 1 of the 3 exercises or none. We will assess whether the 2 feedback types and the 3 microinterventions increase proximal outcomes at the following time point. The microrandomized trial is part of the PerPAIN randomized controlled trial (German Clinical Trials Register DRKS00022792) investigating a personalized treatment approach to enhance treatment outcomes in CMSP.

RESULTS

Approval was granted by the Ethics Committee II of the University of Heidelberg on August 4, 2020. Recruitment for the microrandomized trial began in May 2021 and is ongoing at the time of submission. By October 10, 2022, a total of 24 participants had been enrolled in the microrandomized trial.

CONCLUSIONS

This trial will provide evidence on the feasibility of the PerPAIN app and the initial signals of efficacy of the different intervention components. In the next step, the intervention would need to be further refined and investigated in a definitive trial. This ecological momentary intervention presents a potential method for offering low-level accessible treatment to a wide range of people, which could have substantial implications for public health by reducing disease burden of chronic pain in the population.

INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/43376.

摘要

背景

慢性肌肉骨骼疼痛(CMSP)影响着13%至47%的人口,在过去15年中全球增长率为20.3%,这表明对有效治疗的需求很高。长期以来,疼痛日记一直是非药物疼痛治疗中的常用工具,用于监测和提供患者日常生活症状的反馈。最近,积极重新聚焦技术开始被使用,促进无痛发作和积极结果,而不是专注于疼痛管理。

目的

本研究旨在评估PerPAIN应用程序对CMSP患者进行生态瞬时干预的可行性(即可接受性、干预依从性和保真度)和初步疗效信号。该应用程序包括使用经验抽样法(ESM)进行数字化监测和反馈。此外,患者还会接受3种针对将注意力重新聚焦于积极事件的微干预。

方法

在一项微随机试验中,我们将招募35名CMSP患者,为他们提供该应用程序12周。参与者将被提示每天填写4份ESM监测问卷,评估他们当前的情况以及近端结果变量的信息:无疼痛、积极情绪和主观活动。参与者将每天和每周随机分组,以接收关于ESM评估的近端结果的无反馈、口头反馈或视觉反馈。此外,该应用程序将鼓励参与者基于积极心理学和认知行为疗法技术完成3种微干预。这些微干预是提示报告愉快时刻和日常成功或计划愉快活动。在分别熟悉每种微干预后,参与者将每天随机分组,接受3种练习中的1种或不接受任何练习。我们将评估这2种反馈类型和3种微干预在接下来的时间点是否会增加近端结果。该微随机试验是PerPAIN随机对照试验(德国临床试验注册DRKS00022792)的一部分,该试验正在研究一种个性化治疗方法以提高CMSP的治疗效果。

结果

2020年8月4日,海德堡大学伦理委员会II批准了该研究。微随机试验的招募工作于2021年5月开始,在提交本文时仍在进行中。截至2022年10月10日,共有24名参与者参加了微随机试验。

结论

该试验将为PerPAIN应用程序的可行性以及不同干预成分的初步疗效信号提供证据。在下一步中,需要在确定性试验中对干预进行进一步完善和研究。这种生态瞬时干预为向广泛人群提供低水平可及的治疗提供了一种潜在方法,通过减轻人群中慢性疼痛的疾病负担,可能对公共卫生产生重大影响。

国际注册报告识别码(IRRID):DERR1-10.2196/43376。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7f3/10551789/8c82c6c4c6c3/resprot_v12i1e43376_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7f3/10551789/8c82c6c4c6c3/resprot_v12i1e43376_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7f3/10551789/8c82c6c4c6c3/resprot_v12i1e43376_fig1.jpg

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本文引用的文献

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