Tai Chi Easy for Opioid Use Disorder: Pilot Feasibility Outcomes and Lessons Learned.

IF 1.7 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE
Zhanette Coffee, Terry A Badger, Ruth Taylor-Piliae, Todd W Vanderah, Chong Ho Yu, Judith S Gordon
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Abstract

Background: Opioid use disorder (OUD) remains a global crisis, with chronic pain (CP), anxiety, and opioid cravings contributing to treatment discontinuation and return to opioid use. Despite the effectiveness of medications for OUD (MOUD) such as buprenorphine and methadone, they are underutilized, with nearly 50% of individuals discontinuing prematurely or returning to opioid use. Mind-body therapies (e.g., mindfulness, acupuncture, Tai Chi) have shown promise in reducing stress, drug cravings, and pain while improving well-being. However, Tai Chi has not been systematically tested for individuals with OUD and co-occurring CP and anxiety. The authors aimed to evaluate the feasibility of a virtual Tai Chi Easy (vTCE) intervention as an adjunct therapy for adults with OUD and co-occurring CP, and/or anxiety. Methods: A theory-driven, pre-post, single-group quasi-experimental design was used to evaluate intervention feasibility benchmarks and conduct baseline comparisons between inpatient and outpatient participants. The 8-week vTCE intervention consisted of gentle movements, breathing exercises, self-massage, and mindfulness practices, integrating these components into a holistic mind-body approach. Results: Of 32 screened individuals, 19 enrolled and 15 participated. Recruitment goals were partially met after expanding to outpatient settings (65% of the target). Retention was low, with only 3 participants (15.8%) completing the final assessment. Presurvey completion was high (95%), but postsurvey completion was limited (15.7%). Adherence was low, with only 20% attending more than one session. Acceptability and appropriateness averaged 3.5/5, and feasibility reached 4/5. No injuries were reported, supporting intervention safety. Conclusion: The vTCE intervention was not feasible in the inpatient setting. Outpatient settings showed greater feasibility, with notable differences in baseline characteristics, including self-reported opioid cravings. Lessons learned from this pilot study highlight the need to tailor recruitment, retention, and intervention strategies for future research testing vTCE as an adjunct therapy for individuals with OUD and co-occurring symptoms receiving outpatient MOUD. Trial Registration: ClinicalTrials.gov (Identifier: NCT05850533). Registered: 04/25/2023.

太极易于阿片类药物使用障碍:试点可行性结果和经验教训。
背景:阿片类药物使用障碍(OUD)仍然是一个全球性的危机,慢性疼痛(CP)、焦虑和阿片类药物渴望导致治疗中断和重新使用阿片类药物。尽管丁丙诺啡和美沙酮等治疗OUD的药物有效,但它们未得到充分利用,近50%的人过早停用或重新使用阿片类药物。身心疗法(例如,正念、针灸、太极)在减少压力、对药物的渴望和疼痛,同时提高幸福感方面显示出了希望。然而,太极拳还没有被系统地测试用于患有OUD和同时发生CP和焦虑的个体。作者旨在评估虚拟太极简易(vTCE)干预作为OUD合并CP和/或焦虑的成人辅助治疗的可行性。方法:采用理论驱动、前后、单组准实验设计,评估干预可行性基准,并对住院和门诊参与者进行基线比较。为期8周的vTCE干预包括轻柔的动作、呼吸练习、自我按摩和正念练习,将这些组成部分整合到一个整体的身心方法中。结果:32名筛选个体中,19人入组,15人参与。在扩展到门诊设置后,部分达到了招聘目标(目标的65%)。保留率很低,只有3名参与者(15.8%)完成了最终评估。调查前的完成率很高(95%),但调查后的完成率有限(15.7%)。依从性很低,只有20%的人参加了一次以上的治疗。可接受性和适宜性平均为3.5/5,可行性达到4/5。无人员伤亡报告,表明干预措施是安全的。结论:vTCE干预在住院患者中不可行。门诊设置显示更大的可行性,基线特征显着差异,包括自我报告的阿片类药物渴望。从这项试点研究中吸取的经验教训强调,有必要为未来的研究量身定制招募、保留和干预策略,以测试vTCE作为OUD患者和门诊mod并发症状的辅助治疗。试验注册:ClinicalTrials.gov(标识符:NCT05850533)。注册:04/25/2023。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
4.30
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