VA Connecticut Healthcare System, West Haven, Connecticut.
Yale University, New Haven, Connecticut.
Pain Med. 2020 Dec 12;21(12 Suppl 2):S110-S117. doi: 10.1093/pm/pnaa334.
Veterans with significant chronic pain from musculoskeletal disorders are at risk of substance misuse. Veterans whose condition is the result of military service may be eligible for a disability pension. Department of Veterans Affairs compensation examinations, which determine the degree of disability and whether it was connected to military service, represent an opportunity to engage Veterans in pain management and substance use treatments. A multisite randomized clinical trial is testing the effectiveness and cost-effectiveness of Screening, Brief Intervention, and Referral to Treatment for Pain Management (SBIRT-PM) for Veterans seeking compensation for musculoskeletal disorders. This telephone-based intervention is delivered through a hub-and-spoke configuration.
This study is a two-arm, parallel-group, 36-week, multisite randomized controlled single-blind trial. It will randomize 1,100 Veterans experiencing pain and seeking service-connection for musculoskeletal disorders to either SBIRT-PM or usual care across eight New England VA medical centers. The study balances pragmatic with explanatory methodological features. Primary outcomes are pain severity and number of substances misused. Nonpharmacological pain management and substance use services utilization are tracked in the trial.
Early trial enrollment targets were met across sites. SBIRT-PM could help Veterans, at the time of their compensation claims, use multimodal pain treatments and reduce existing substance misuse. Strategies to address COVID-19 pandemic impacts on the SBIRT-PM protocol have been developed to maintain its pragmatic and exploratory integrity.
患有肌肉骨骼疾病导致严重慢性疼痛的退伍军人有滥用药物的风险。因军事服务导致患病的退伍军人可能有资格获得残疾抚恤金。退伍军人事务部的补偿检查可以确定残疾程度以及是否与军事服务有关,这为退伍军人参与疼痛管理和药物使用治疗提供了机会。一项多地点随机临床试验正在测试针对因肌肉骨骼疾病寻求赔偿的退伍军人的疼痛管理筛查、简短干预和转介治疗(SBIRT-PM)的有效性和成本效益。这种基于电话的干预措施通过枢纽和辐条配置提供。
本研究是一项为期 36 周的、两臂、平行组、多地点随机对照单盲试验。它将在 8 个新英格兰 VA 医疗中心,将 1100 名经历疼痛并寻求与肌肉骨骼疾病有关的服务连接的退伍军人随机分配到 SBIRT-PM 或常规护理组。该研究平衡了实用和解释性的方法学特征。主要结局是疼痛严重程度和滥用物质的数量。非药物性疼痛管理和药物使用服务的使用情况在试验中进行了跟踪。
各地点都达到了早期试验入组的目标。SBIRT-PM 可以帮助退伍军人在提出赔偿申请时使用多模式疼痛治疗方法,并减少现有的药物滥用。为了保持 SBIRT-PM 方案的实用性和探索性完整性,已经制定了应对 COVID-19 大流行影响的策略。