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Effectiveness of a cognitive-behavioral group intervention for knee osteoarthritis pain: protocol of a randomized controlled trial

机译:认知行为干预干预对膝骨关节炎疼痛的有效性:一项随机对照试验的方案

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Background Knee osteoarthritis is the most common type of arthritis, with pain being its most common symptom. Little is known about the psychological aspects of knee osteoarthritis pain. There is an emerging consensus among osteoarthritis specialists about the importance of addressing not only biological but also psychosocial factors in the assessment and treatment of osteoarthritis. As few studies have evaluated the effect of psychological interventions on knee osteoarthritis pain, good quality randomized controlled trials are needed to determine their effectiveness. Methods/Design We intend to conduct a 6-week single-blinded randomized controlled trial with a 12-month follow-up. Altogether, 108 patients aged from 35 to 75 years with clinical symptoms and radiographic grading (KL 2–4) of knee osteoarthritis will be included. The clinical inclusion criteria are pain within the last year in or around the knee occurring on most days for at least one month, and knee pain of ≥40 mm on a 100-mm visual analogue scale in the WOMAC pain subscale for one week prior to study entry. Patients with any severe psychiatric disorder, other back or lower limb pain symptoms more aggravating than knee pain, or previous or planned lower extremity joint surgery will be excluded. The patients will be randomly assigned to a combined GP care and cognitive-behavioral intervention group (n = 54) or to a GP care control group (n = 54). The cognitive-behavioral intervention will consist of 6 weekly group sessions supervised by a psychologist and a physiotherapist experienced in the treatment of pain. The main goals of the intervention are to reduce maladaptive pain coping and to increase the self-management of pain and disability. The follow-up-points will be arranged at 3 and 12 months. The primary outcome measure will be the WOMAC pain subscale. Secondary outcome measures will include self-reports of pain and physical function, a health related quality of life questionnaire, and various psychological questionnaires. Personnel responsible of the data analysis will be blinded. Discussion This study addresses the current topic of non-pharmacological conservative treatment of knee OA-related pain. We anticipate that these results will provide important new insights to the current care recommendations. Trial registration Current Controlled Trials ISRCTN64794760
机译:背景技术膝骨关节炎是最常见的关节炎类型,疼痛是其最常见的症状。关于膝骨关节炎疼痛的心理方面知之甚少。骨关节炎专家之间正在出现一个新的共识,即在评估和治疗骨关节炎中不仅要解决生物学因素,还要解决社会心理因素的重要性。由于很少有研究评估心理干预对膝骨关节炎疼痛的影响,因此需要高质量的随机对照试验来确定其有效性。方法/设计我们打算进行为期6周的单盲随机对照试验,并进行12个月的随访。总共包括108名年龄在35至75岁之间且具有膝骨关节炎的临床症状和影像学分级(KL 2–4)的患者。临床入选标准是在过去一年中大部分时间内在膝盖内或膝盖周围发生疼痛至少一个月,并且在WOMAC疼痛亚评分中以100 mm视觉模拟量表在≥40 mm的膝盖疼痛发生前一个星期。学习条目。患有任何严重精神病,其他比膝盖疼痛更严重的背部或下肢疼痛症状的患者,或先前或计划进行的下肢关节手术的患者将被排除在外。将患者随机分为GP护理和认知行为干预组(n = 54)或GP护理对照组(n = 54)。认知行为干预将由在疼痛治疗方面经验丰富的心理学家和物理治疗师监督下的每周六次小组会议组成。干预的主要目标是减少适应不良的疼痛应对并增加对疼痛和残疾的自我管理。随访时间将安排在3个月和12个月。主要结果指标将是WOMAC疼痛量表。次要结局指标将包括疼痛和身体功能的自我报告,与健康相关的生活质量调查表以及各种心理调查表。负责数据分析的人员将不知情。讨论本研究解决了膝骨关节炎相关疼痛的非药物保守治疗的当前主题。我们预计这些结果将为当前的护理建议提供重要的新见解。试用注册电流对照试验ISRCTN64794760

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