基于体育锻炼、正念、行为改变和教育的多模式干预改善慢性原发性腰痛患者的疼痛和健康:HEALTHYBACK随机对照试验的研究方案

IF 3.9 Q1 SPORT SCIENCES
BMJ Open Sport & Exercise Medicine Pub Date : 2024-11-21 eCollection Date: 2024-01-01 DOI:10.1136/bmjsem-2024-002188
Gavriella Tsiarleston, María Dolores López-Fernández, Rodrigo Pavón-Muñoz, Iván Aguilera-García, María López-Corchón, Manuel Delgado-Fernández, María Yolanda Castellote-Caballero, Belén Donoso, Antonio Manuel Mesa-Ruiz, Rocío Pozuelo-Calvo, Ángela María Ríos-Ortiz, Gemma Álvarez-Corral, Nuria Marín-Jiménez, Dario Martinez-Garcia, Ignacio Jesús Chirosa Ríos, Víctor Segura-Jiménez
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引用次数: 0

摘要

HEALTHYBACK试验基于多模式干预,以确定有监督的体育锻炼、正念、行为改变和疼痛神经科学教育计划对慢性原发性腰痛(CPLBP)患者几个健康变量的有效性。该研究将是一项随机对照试验,纳入70名确诊为CPLBP的患者(年龄18-65岁)。干预将在医院环境中亲自进行,为期16周,包括第一阶段(16次有监督的体育锻炼(2天/周,45分钟/次),正念(1天/周,2.5小时/次),行为改变(每天/24小时,通过腕带活动提示装置)和疼痛神经科学教育(1天/双周,2小时/次))和第二阶段(16次全身肌肉强化锻炼,3天/周,50分钟/次)。主要结果将包括感知到的急性疼痛、疼痛压力阈值、条件疼痛调节、疼痛的时间总和和疼痛引起的残疾。次要测量将包括身体健康、身体组成、步态参数、设备测量的身体活动和久坐行为、血液学特征、自我报告的久坐行为、生活质量、疼痛灾难、心理健康、睡眠持续时间和质量以及与中枢敏感化相关的症状。各组将进行前测(干预前)、后测(干预各阶段后)和复测(干预后6周去训练期)测量。结果将确定对CPLBP患者的几个健康参数进行多维干预的有效性。他们将为受影响个人的疼痛管理和功能提供知识,这可能会减少对初级保健服务的需求。试验注册号:NCT06114264。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multimodal intervention based on physical exercise, mindfulness, behaviour change and education to improve pain and health in patients with chronic primary low back pain: a study protocol of the HEALTHYBACK randomised controlled trial.

The HEALTHYBACK trial is based on a multimodal intervention to determine the effectiveness of a supervised physical exercise, mindfulness, behaviour change and pain neuroscience education programme on several health variables in individuals with chronic primary low back pain (CPLBP). The study will be a randomised controlled trial among 70 individuals diagnosed with CPLBP (aged 18-65 years). The intervention will be conducted in person within a hospital setting for 16 weeks and comprises a first phase (16 sessions supervised physical exercise (2 days/week, 45 min/session), mindfulness (1 day/week, 2.5 hours/session), behaviour change (daily/24 hours via a wrist-worn activity prompting device) and pain neuroscience education (1 day/biweekly, 2 hours/session)) and a second phase (16 sessions functional full-body muscle strengthening exercise, 3 days/week, 50 min/session). The primary outcomes will include perceived acute pain, pain pressure threshold, conditioned pain modulation, temporal summation of pain and disability due to pain. Secondary measures will include physical fitness, body composition, gait parameters, device-measured physical activity and sedentary behaviour, haematological profile, self-reported sedentary behaviour, quality of life, pain catastrophising, mental health, sleep duration and quality, and symptoms related to central sensitisation. The groups will undergo pretest (before the intervention), post-test (after each phase of the intervention) and retest (at a 6-week detraining period after the intervention) measurements. The results will determine the effectiveness of multidimensional interventions on several health parameters in individuals with CPLBP. They will provide knowledge for pain management and functioning in affected individuals, which might diminish the need for primary healthcare services. Trial registration number: NCT06114264.

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来源期刊
CiteScore
7.10
自引率
4.20%
发文量
106
审稿时长
20 weeks
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