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Chronic pain self-management support with pain science education and exercise (COMMENCE): study protocol for a randomized controlled trial

机译:慢性疼痛自我管理支持与疼痛科学教育和锻炼(开始):一项随机对照试验的研究方案

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Background Previous research suggests that self-management programs for people with chronic pain improve knowledge and self-efficacy but result in negligible effects on function. This study will investigate the effectiveness self-management support with pain science education and exercise on improving function for people with chronic pain in comparison to a wait-list control. A secondary objective is to determine which variables help to predict response to the intervention. Methods/Design This study will be an unblinded, randomized controlled trial with 110 participants comparing a 6-week program that includes self-management support, pain science education and exercise to a wait-list control. The primary outcome will be function measured by the Short Musculoskeletal Function Assessment - Dysfunction Index. Secondary outcomes will include pain intensity measured by a numeric pain rating scale, pain interference measured by the eight-item PROMIS pain interference item-bank, how much patients are bothered by functional problems measured by the Short Musculoskeletal Function Assessment - Bother Index, catastrophic thinking measured by the Pain Catastrophizing Scale, fear of movement/re-injury measured by the 11-item Tampa Scale of Kinesiophobia, sense of perceived injustice measured by the Injustice Experience Questionnaire, self-efficacy measured by the Pain Self-Efficacy Questionnaire, pain sensitivity measured by pressure pain threshold and cold sensitivity testing, fatigue measured by a numeric fatigue rating scale, pain neurophysiology knowledge measured by the Neurophysiology of Pain Questionnaire, healthcare utilization measured by number of visits to a healthcare provider, and work status. Assessments will be completed at baseline, 7 and 18?weeks. After the 18-week assessment, the groups will crossover; however, we anticipate carry-over effects with the treatment. Therefore, data from after the crossover will be used to estimate within-group changes and to determine predictors of response that are not for direct between-group comparisons. Mixed effects modelling will be used to determine between-group differences for all primary and secondary outcomes. A series of multiple regression models will be used to determine predictors of treatment response. Discussion This study has the potential to inform future self-management programming through evaluation of a self-management program that aims to improve function as the primary outcome. Trial registration ClinicalTrials.gov NCT02422459 , registered on 13 April 2015.
机译:背景技术先前的研究表明,针对慢性疼痛患者的自我管理计划可以提高知识和自我效能,但对功能的影响却可以忽略不计。这项研究将通过疼痛科学教育调查自我管理支持的有效性,并通过锻炼来改善慢性疼痛患者的功能(与等待名单控制相比)。第二个目标是确定哪些变量有助于预测对干预的反应。方法/设计这项研究将是一项无盲,随机对照的试验,共有110名参与者,将为期6周的计划(包括自我管理支持,疼痛科学教育和锻炼与等待名单控制)进行了比较。主要结果将通过短肌骨骼功能评估-功能障碍指数来衡量。次要结果将包括通过数字疼痛等级量表测量的疼痛强度,通过8个项目的PROMIS疼痛干预项目库测量的疼痛干扰,通过短期骨骼骨骼功能评估-干扰指数测量的功能性问题困扰多少患者,灾难性思维通过疼痛灾难性量表进行测量,通过恐惧症的11个项目坦帕量表测量对运动/再伤害的恐惧,通过不公正经历调查表进行测量以感知不公正感,通过疼痛自我效能调查表进行测量以评估自我效能,疼痛敏感性通过压力疼痛阈值和冷敏感度测试测量疲劳,通过数字疲劳等级量表测量疲劳,通过疼痛问卷神经生理学测量疼痛神经生理学知识,通过就诊医疗人员就诊次数测量医疗保健利用率,以及工作状态。评估将在基线的第7周和第18周完成。经过18周的评估,小组将进行交叉交流;但是,我们预计该处理会带来残留效应。因此,交叉后的数据将用于估计组内变化并确定不适用于组间直接比较的响应预测变量。混合效应模型将用于确定所有主要和次要结果的组间差异。一系列多元回归模型将用于确定治疗反应的预测因子。讨论本研究通过评估旨在改善功能作为主要结果的自我管理计划,有可能为将来的自我管理计划提供参考。试用注册ClinicalTrials.gov NCT02422459,于2015年4月13日注册。

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