慢性腰痛管理:多模式方法的临床和心理生理结果——一项关于瑜伽和正念的随机对照试验。

IF 3.9 Q1 SPORT SCIENCES
BMJ Open Sport & Exercise Medicine Pub Date : 2025-06-08 eCollection Date: 2025-01-01 DOI:10.1136/bmjsem-2025-002697
Yusra Saleem, Shamoon Noushad, Sadaf Ahmed, Basit Ansari
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引用次数: 0

摘要

慢性腰痛(CLBP)是一个广泛存在的医学问题,严重影响个人健康状况,同时产生大量的经济支出。传统的治疗方法往往效果有限,因此有必要探索替代疗法,如瑜伽和正念减压(MBSR)。本研究旨在比较狮身人面像体式瑜伽和正念减压对CLBP的治疗效果。重点是评估疼痛强度、功能残疾、生活质量、心率变异性和与CLBP相关的生理指标的改善。这项多中心平行随机对照试验将比较瑜伽和正念减压对医疗保健提供者CLBP的疗效。参与者将被随机分配到四组:狮身人面像瑜伽疗法(A组)、正念减压疗法(B组)、常规护理(C组)和瑜伽-正念减压疗法联合干预(D组)。每次干预将持续12周。主要结局包括疼痛强度、功能障碍(Oswestry问卷)和生理指标(皮质醇、β-内啡肽、p物质、白细胞介素-6、C反应蛋白)。次要结局包括生活质量(世卫组织生活质量)、压力(Sadaf压力量表)、抑郁(Beck抑郁量表)、焦虑(广泛性焦虑症-7)和心率变异性。数据将在基线(第0周)、干预结束(第12周)和干预后12周(第24周)收集。试验注册号NCT06910982。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chronic low back pain management: clinical and psychophysiological outcomes of multimodal approaches-a randomised controlled trial on yoga and mindfulness.

Chronic low back pain (CLBP) presents as a widespread medical issue which severely affects personal health status while generating substantial economic expenses. Traditional treatment methods often have limited efficacy, necessitating the exploration of alternative therapies such as yoga and mindfulness-based stress reduction (MBSR). This study aims to compare the efficacy of Sphinx pose yoga and MBSR in managing CLBP. The focus is on evaluating improvements in pain intensity, functional disability, quality of life, heart rate variability and physiological markers associated with CLBP. This multicentre parallel-arm randomised controlled trial will compare the efficacy of yoga to MBSR for CLBP in healthcare providers. Participants will be randomly assigned to one of four groups: Sphinx pose yoga therapy (Group A), MBSR (Group B), usual care (Group C) and a combined yoga-MBSR intervention (Group D). Each intervention will last 12 weeks. Primary outcomes include pain intensity, functional disability (Oswestry Questionnaire) and physiological markers (cortisol, β-endorphins, substance-P, interleukin-6, C reactive protein). Secondary outcomes encompass quality of life (WHO Quality of Life), stress (Sadaf Stress Scale), depression (Beck Depression Inventory), anxiety (Generalised Anxiety Disorder-7) and heart rate variability. Data will be collected at baseline (week 0), at the end of the intervention (week 12) and 12 weeks after the intervention (week 24). Trial registration number NCT06910982.

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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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