Schuman-Olivier Zev, Goodman Hannah, Rosansky Joseph, Fredericksen Alaine Kiera, Barria Javier, Parry Gareth, Sokol Randi, Gardiner Paula, Lê Cook Benjamin, Weiss Roger D
Department of Psychiatry, Cambridge Health Alliance, Malden, Massachusetts.
Department of Psychiatry, Harvard Medical School, Boston, Massachusetts.
JAMA Netw Open. 2025 Jan 2;8(1):e2454950. doi: 10.1001/jamanetworkopen.2024.54950.
During buprenorphine treatment for opioid use disorder (OUD), risk factors for opioid relapse or treatment dropout include comorbid substance use disorder, anxiety, or residual opioid craving. There is a need for a well-powered trial to evaluate virtually delivered groups, including both mindfulness and evidence-based approaches, to address these comorbidities during buprenorphine treatment.
To compare the effects of the Mindful Recovery Opioid Use Disorder Care Continuum (M-ROCC) vs active control among adults receiving buprenorphine for OUD.
DESIGN, SETTING, AND PARTICIPANTS: This randomized clinical trial was conducted from January 21, 2021, to September 19, 2023. All study procedures were conducted virtually. Participants were randomized 1:1 and blinded to intervention assignments throughout participation. This trial recruited online from 16 US states and was conducted via online platforms. Patients prescribed buprenorphine for OUD were recruited via social media advertisements, flyers, and health care professional referrals.
The M-ROCC program was a 24-week, motivationally adaptive, trauma-informed, mindfulness-based group curriculum. Participants attended a 30-minute informal check-in and 60-minute intervention group each week. The recovery support group control curriculum used 4 evidence-based substance use disorder-focused nonmindfulness approaches and was time and attention matched.
The primary outcome was the number of 2-week periods with both self-reported and biochemically confirmed abstinence from illicit opioid use during study weeks 13 to 24, which was analyzed with an intention-to-treat approach using generalized estimating equations comparing between-group differences.
This sample included 196 participants, predominantly female (119 [60.7%]). Mean (SD) age was 41.0 (10.3) years. Opioid use was 13.4% (95% CI, 6.2%-20.5%) in the M-ROCC group and 12.7% (95% CI, 7.5%-18.0%) in the recovery support group, a 0.6% difference (95% CI, -8.2% to 9.5%; P = .89). Cocaine and benzodiazepine use were also not significantly different. Anxiety T scores were reduced across both the M-ROCC and recovery support groups but were not significantly different between groups from baseline to week 24 (1.0; 95% CI, -2.4 to 4.3; P = .57). The M-ROCC participants demonstrated a larger reduction in opioid craving compared with the recovery support group participants: -1.0 (95% CI, -1.7 to -0.2; P = .01; Cohen d = -0.5).
In this study, during buprenorphine treatment comparing mindfulness vs active control, both groups significantly reduced anxiety without significant differences in substance use outcomes. Mindfulness led to significantly greater reductions in residual opioid craving than control. The findings of this study suggest that mindfulness training groups may be recommended for people receiving buprenorphine maintenance therapy who have residual opioid craving.
ClinicalTrials.gov Identifier: NCT04278586.
在丁丙诺啡治疗阿片类物质使用障碍(OUD)期间,阿片类物质复发或治疗中断的风险因素包括共病物质使用障碍、焦虑或残留的阿片类物质渴望。需要进行一项有足够效力的试验来评估虚拟提供的干预组,包括正念和循证方法,以解决丁丙诺啡治疗期间的这些共病情况。
比较正念康复阿片类物质使用障碍护理连续体(M-ROCC)与接受丁丙诺啡治疗OUD的成年人中的积极对照的效果。
设计、设置和参与者:这项随机临床试验于2021年1月21日至2023年9月19日进行。所有研究程序均以虚拟方式进行。参与者按1:1随机分组,在整个参与过程中对干预分配不知情。该试验从美国16个州在线招募,并通过在线平台进行。因OUD而开具丁丙诺啡处方的患者通过社交媒体广告、传单和医疗保健专业人员推荐招募。
M-ROCC计划是一个为期24周、具有动机适应性、创伤知情、基于正念的团体课程。参与者每周参加一次30分钟的非正式报到和一次60分钟的干预组课程。康复支持组对照课程使用4种以循证物质使用障碍为重点的非正念方法,在时间和关注度上相匹配。
主要结局是在研究第13至24周期间,自我报告且经生化确认戒除非法阿片类物质使用的2周时间段的数量,采用意向性分析方法,使用广义估计方程比较组间差异。
该样本包括196名参与者,主要为女性(119名[60.7%])。平均(标准差)年龄为41.0(10.3)岁。M-ROCC组的阿片类物质使用为13.4%(95%CI,6.2%-20.5%),康复支持组为12.7%(95%CI,7.5%-18.0%),差异为0.6%(95%CI,-8.2%至9.5%;P = 0.89)。可卡因和苯二氮䓬类药物的使用也无显著差异。M-ROCC组和康复支持组的焦虑T分数均有所降低,但从基线到第24周,两组之间无显著差异(1.0;95%CI,-2.4至4.3;P = 0.57)。与康复支持组参与者相比,M-ROCC参与者在阿片类物质渴望方面的降低幅度更大:-1.0(95%CI,-1.7至-0.2;P = 0.01;Cohen d = -0.5)。
在本研究中,在丁丙诺啡治疗期间比较正念与积极对照时,两组均显著降低了焦虑,物质使用结局无显著差异。正念导致残留阿片类物质渴望的降低幅度明显大于对照。本研究结果表明,对于接受丁丙诺啡维持治疗且有残留阿片类物质渴望的人,可能推荐正念训练组。
ClinicalTrials.gov标识符:NCT04278586。