Kaiser Permanente Center for Health Research, Portland, OR, United States.
Kaiser Permanente Center for Health Research, Portland, OR, United States; University of Portland, School of Nursing, Portland, OR, United States.
Contemp Clin Trials. 2018 Apr;67:91-99. doi: 10.1016/j.cct.2018.02.015. Epub 2018 Mar 6.
Chronic pain is one of the most common, disabling, and expensive public health problems in the United States. Interdisciplinary pain management treatments that employ behavioral approaches have been successful in helping patients with chronic pain reduce symptoms and regain functioning. However, most patients lack access to such treatments. We are conducting a pragmatic clinical trial to test the hypothesis that patients who receive an interdisciplinary biopsychosocial intervention, the Pain Program for Active Coping and Training (PPACT), at their primary care clinic will have a greater reduction in pain impact in the year following than patients receiving usual care.
METHODS/DESIGN: This is an effectiveness-implementation hybrid pragmatic clinical trial in which we randomize clusters of primary care providers and their patients with chronic pain who are on long-term opioid therapy to 1) receive an interdisciplinary behavioral intervention in conjunction with their current health care or 2) continue with current health care services. Our primary outcome is pain impact (a composite of pain intensity and pain-related interference) measured using the PEG, a validated three-item assessment. Secondary outcomes include pain-related disability, patient satisfaction, opioids dispensed and health care utilization. An economic evaluation assesses the resources and costs necessary to deliver the intervention and its cost-effectiveness compared with usual care. A formative evaluation employs mixed methods to understand the context for implementation in the participating health care systems.
This trial will inform the feasibility of implementing interdisciplinary behavioral approaches to pain management in the primary care setting, potentially providing a more effective, safer, and more satisfactory alternative to opioid-based chronic pain treatment. Clinical Trials Registration Number: NCT02113592.
慢性疼痛是美国最常见、最具致残性和最昂贵的公共卫生问题之一。采用行为方法的跨学科疼痛管理治疗方法已成功帮助慢性疼痛患者减轻症状并恢复功能。然而,大多数患者无法获得此类治疗。我们正在进行一项实用的临床试验,以检验以下假设:在初级保健诊所接受跨学科生物心理社会干预(积极应对和培训疼痛计划,即 PPACT)的患者,在接下来的一年中疼痛影响会比接受常规护理的患者更大。
方法/设计:这是一项有效性-实施混合实用临床研究,我们将长期接受阿片类药物治疗的慢性疼痛的初级保健提供者及其患者进行聚类随机分组,分别接受 1)接受跨学科行为干预与他们当前的医疗保健相结合,或 2)继续接受当前的医疗保健服务。我们的主要结局是使用 PEG(一种经过验证的三项评估)测量的疼痛影响(疼痛强度和与疼痛相关的干扰的综合)。次要结局包括疼痛相关残疾、患者满意度、阿片类药物的配给和医疗保健的利用。经济评估评估提供干预措施所需的资源和成本,以及与常规护理相比的成本效益。形成性评估采用混合方法了解参与医疗保健系统实施的背景。
该试验将为在初级保健环境中实施跨学科行为方法治疗疼痛提供可行性信息,为基于阿片类药物的慢性疼痛治疗提供更有效、更安全、更令人满意的替代方法。临床试验注册号:NCT02113592。