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Twelve-month effect of chronic pain self-management intervention delivered in an easily accessible primary healthcare service - a randomised controlled trial

机译:慢性疼痛自我管理干预的12个月效果在易于访问的主要医疗保健服务中交付 - 随机对照试验

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摘要

Abstract Background To investigate the effects after twelve months related to patient activation and a range of secondary outcomes on persons with chronic pain of a chronic pain self-management course compared to a low-impact outdoor physical activity, delivered in an easily accessible healthcare service in public primary care. Methods An open, pragmatic, parallel group randomised controlled trial was conducted. The intervention group was offered a group-based chronic pain self-management course with 2.5-h weekly sessions for a period of six weeks comprising education that included cognitive and behavioural strategies for pain management, movement exercises, group discussions and sharing of experiences among participants. The control group was offered a drop-in, low-impact, outdoor physical activity in groups in one-hour weekly sessions that included walking and simple strength exercises for a period of six weeks. The primary outcome was patient activation assessed using the Patient Activation Measure (PAM-13). Secondary outcomes included assessments of pain, anxiety and depression, pain self-efficacy, sense of coherence, health-related quality of life, well-being and the 30-s Chair to Stand Test. Analyses were performed using a linear mixed model. Results After twelve months, there were no statistically significant differences between the intervention group (n = 60) and the control group (n = 61) for the primary or the secondary outcomes. The estimated mean difference between the groups for the primary outcome PAM was 4.0 (CI 95% -0.6 to 8.6, p = 0.085). Within both of the groups, there were statistically significant improvements in pain experienced during the previous week, the global self-rated health measure and the 30-s Chair to Stand Test. Conclusions No long-term effect of the chronic pain self-management course was found in comparison with a low-impact physical activity intervention for the primary outcome patient activation or for any secondary outcome. Trial registration ClinicalTrials.gov: NCT02531282. Registered on August 212,015
机译:摘要背景,探讨了与患者激活和一系列慢性疼痛自我管理课程的慢性疼痛的慢性疼痛的次要成果相关的疗效和一系列二次结果的影响,而在易于访问的医疗保健服务中交付公共初级保健。方法进行开放,务实,并行组随机对照试验。干预小组被提供基于组的慢性疼痛自我管理课程,每周六周的时间为2.5小时,包括包括教育,包括认知和行为策略的痛苦管理,运动锻炼,集团讨论和参与者之间的经验。对照组在一小时的每周会话中,在一小时的每周举行的群体中提供了一个下降,低影响,包括步行和简单的力量练习六周。主要结果是使用患者激活测量(PAM-13)评估的患者激活。二次结果包括疼痛,焦虑和抑郁,疼痛自我效能,连贯性,健康状况,生活质量,福祉和30脚椅进行试验的评估。使用线性混合模型进行分析。结果12个月后,干预组(N = 60)与初级或二次结果的干预组(N = 60)和对照组(N = 61)之间没有统计学上显着差异。初级结果PAM的群体之间的估计平均差异为4.0(CI 95%-0.6至8.6,P = 0.085)。在这两个团体中,前一周的痛苦,全球自我评价的健康措施和30-S椅进行了统计上显着的改善。结论与初级结果患者激活或任何次要结果的低抗冲击性能干预相比,没有发现慢性疼痛自我管理课程的长期效果。试验登记ClinicalTrials.gov:NCT02531282。在8月21,015注册

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