Kaiser Permanente Washington Health Research Institute, Seattle, WA, United States of America; The Center for Health Research, Kaiser Permanente Northwest, Portland, OR, United States of America.
Indiana University School of Medicine, Department of Psychiatry, Indianapolis, IN, United States of America.
Contemp Clin Trials. 2023 Apr;127:107124. doi: 10.1016/j.cct.2023.107124. Epub 2023 Feb 18.
Opioid use disorder (OUD) contributes to rising morbidity and mortality. Life-saving OUD treatments can be provided in primary care but most patients with OUD don't receive treatment. Comorbid depression and other conditions complicate OUD management, especially in primary care. The MI-CARE trial is a pragmatic randomized encouragement (Zelen) trial testing whether offering collaborative care (CC) to patients with OUD and clinically-significant depressive symptoms increases OUD medication treatment with buprenorphine and improves depression outcomes compared to usual care.
Adult primary care patients with OUD and depressive symptoms (n ≥ 800) from two statewide health systems: Kaiser Permanente Washington and Indiana University Health are identified with computer algorithms from electronic Health record (EHR) data and automatically enrolled. A random sub-sample (50%) of eligible patients is offered the MI-CARE intervention: a 12-month nurse-driven CC intervention that includes motivational interviewing and behavioral activation. The remaining 50% of the study cohort comprise the usual care comparison group and is never contacted. The primary outcome is days of buprenorphine treatment provided during the intervention period. The powered secondary outcome is change in Patient Health Questionnaire (PHQ)-9 depression scores. Both outcomes are obtained from secondary electronic healthcare sources and compared in "intent-to-treat" analyses.
MI-CARE addresses the need for rigorous encouragement trials to evaluate benefits of offering CC to generalizable samples of patients with OUD and mental health conditions identified from EHRs, as they would be in practice, and comparing outcomes to usual primary care. We describe the design and implementation of the trial, currently underway.
ClinicalTrials.gov Identifier: NCT05122676. Clinical trial registration date: November 17, 2021.
阿片类药物使用障碍(OUD)导致发病率和死亡率上升。救命的 OUD 治疗可以在初级保健中提供,但大多数 OUD 患者没有接受治疗。合并抑郁和其他疾病使 OUD 的管理复杂化,尤其是在初级保健中。MI-CARE 试验是一项实用的随机鼓励(Zelen)试验,旨在测试向患有 OUD 和临床显著抑郁症状的患者提供协作护理(CC)是否会增加丁丙诺啡治疗 OUD 的药物治疗,并与常规护理相比改善抑郁结局。
从两个全州卫生系统(华盛顿州的 Kaiser Permanente 和印第安纳大学健康系统)的电子健康记录 (EHR) 数据中使用计算机算法确定患有 OUD 和抑郁症状的成年初级保健患者(n≥800),并自动纳入研究。合格患者的随机子样本(50%)被提供 MI-CARE 干预措施:为期 12 个月的由护士驱动的 CC 干预措施,包括动机访谈和行为激活。研究队列的其余 50%作为常规护理比较组,从不联系。主要结局是干预期间提供的丁丙诺啡治疗天数。有力的次要结局是患者健康问卷(PHQ)-9 抑郁评分的变化。这两个结局都是从二级电子医疗来源获得的,并在“意向治疗”分析中进行比较。
MI-CARE 满足了严格鼓励试验的需求,以评估向从 EHR 中确定的可推广的 OUD 和心理健康患者群体提供 CC 的益处,就像在实践中一样,并将结果与常规初级保健进行比较。我们描述了该试验的设计和实施情况,目前正在进行中。
ClinicalTrials.gov 标识符:NCT05122676。临床试验注册日期:2021 年 11 月 17 日。