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

被引:6
|
作者
Miller, Jordan [1 ]
MacDermid, Joy C. [1 ]
Walton, David M. [2 ]
Richardson, Julie [1 ]
机构
[1] McMaster Univ, Sch Rehabil Sci, Hamilton, ON L8S 1C7, Canada
[2] Univ Western Ontario, Sch Phys Therapy, London, ON, Canada
关键词
LOW-BACK-PAIN; QUALITY-OF-LIFE; PSYCHOMETRIC PROPERTIES; PRESSURE PAIN; PRIMARY-CARE; NEUROPHYSIOLOGY EDUCATION; DEPRESSION SEVERITY; PROGNOSTIC-FACTORS; PHYSICAL-ACTIVITY; CHRONIC WHIPLASH;
D O I
10.1186/s13063-015-0994-5
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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.
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页数:12
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