Department of Public Health and Nursing, Norwegian University of Science and Technology, Trondheim, Norway
Department of Neurology and Clinical Neurophysiology, St. Olavs Hospital, Trondheim, Norway.
BMJ Open. 2024 Aug 21;14(8):e083592. doi: 10.1136/bmjopen-2023-083592.
Insomnia is prevalent among patients visiting physiotherapists due to musculoskeletal complaints and associated with poorer pain prognosis. Cognitive-Behavioural Therapy for Insomnia (CBT-I) may be effective for improving sleep quality and pain-related outcomes in these patients, but its availability and utility are limited in daily physiotherapy practice. The aim of this randomised controlled trial (RCT) is to evaluate the effectiveness of digital CBT-I in addition to usual treatment in patients with chronic musculoskeletal complaints and insomnia, compared with usual treatment only.
In this RCT, eligible and consenting participants will be randomised (1:1 ratio) to one of two interventions: (1) digital CBT-I adjunct to physiotherapy treatment or (2) usual physiotherapy treatment. Patients with musculoskeletal complaints and insomnia visiting a physiotherapist in Norway will be invited to participate in the study. We aim to include 188 participants to detect a difference in the primary outcome. Outcome variables will be assessed at baseline (prior to randomisation) and at 6-week, 3-month, 6-month and 12-month follow-up. The primary outcome is between-group difference in insomnia severity, assessed with the Insomnia Severity Index (0-28 points) at 3 months. Secondary outcomes include between-group differences in pain intensity, physical function, work ability, health-related quality of life, mental distress, and self-reported use of sleep and pain medication. Exploratory analyses will identify patient characteristics influencing the effect of the digital intervention.
This trial is approved by the Regional Committee for Medical and Health Research Ethics in Central Norway (Ref. 2023/533381). The results of the trial will be published in peer-review journals and disseminated at national and international conferences.
ISRCTN91221906.
由于肌肉骨骼投诉,失眠在看物理治疗师的患者中很普遍,并且与更差的疼痛预后相关。认知行为疗法治疗失眠(CBT-I)可能对改善这些患者的睡眠质量和与疼痛相关的结果有效,但在日常物理治疗实践中,其可用性和实用性有限。本随机对照试验(RCT)的目的是评估数字 CBT-I 在慢性肌肉骨骼投诉和失眠患者中除了常规治疗之外的附加效果,与仅常规治疗相比。
在这项 RCT 中,符合条件并同意的参与者将被随机(1:1 比例)分配到以下两种干预措施之一:(1)数字 CBT-I 辅助物理治疗或(2)常规物理治疗。挪威的物理治疗师将邀请患有肌肉骨骼投诉和失眠的患者参加研究。我们的目标是纳入 188 名参与者以检测主要结局的差异。将在基线(随机分组前)和 6 周、3 个月、6 个月和 12 个月随访时评估结局变量。主要结局是 3 个月时使用失眠严重程度指数(0-28 分)评估的组间差异。次要结局包括疼痛强度、身体功能、工作能力、健康相关生活质量、精神困扰以及自我报告的睡眠和疼痛药物使用情况的组间差异。探索性分析将确定影响数字干预效果的患者特征。
该试验已获得挪威中央地区医学和健康研究伦理委员会的批准(参考号 2023/533381)。试验结果将发表在同行评议期刊上,并在国家和国际会议上传播。
ISRCTN91221906。