针对被监禁者的愤怒管理的瑜伽干预试点随机对照试验。

IF 1.3 4区 医学 Q3 INTEGRATIVE & COMPLEMENTARY MEDICINE
Lisa A Uebelacker, Lindsey Stevens, Hannah Graves, Tosca D Braun, Rebecca Foster, Jennifer E Johnson, Geoffrey Tremont, Lauren M Weinstock
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引用次数: 0

摘要

导言:监禁是改善愤怒和攻击行为自我管理的大好时机。以哈他瑜伽为基础的干预(YBI)可作为监狱内治疗愤怒的有效辅助干预措施。方法:我们招募了 40 名愤怒水平升高的被监禁者(20 名在女子监狱,20 名在男子监狱),进行为期 10 周的 YBI 与健康教育(HE)对照组随机对照试验。参与者每周参加一次各自的小组活动。我们考察了可行性和可接受性指标,包括干预的可信度、对干预会有所帮助的预期、干预的满意度、课堂出勤率、个人实践参与度、指导者的忠诚度、干预的安全性以及研究的招募率和保留率。我们还考察了随着时间的推移,愤怒、抑郁、焦虑和行为违规等临床结果的变化。结果我们在以下几项结果上都达到了目标:YBI 和 HE 干预的可信度、对其有帮助的预期以及对项目的满意度。指导者对两本手册都表现出了忠实性。没有发生与参与研究相关的严重不良事件。在两家机构中,课堂出勤率均未达到我们的目标结果,在男子机构中,个人练习率达到了我们的目标结果,但在女子机构中未达到目标结果。对于参加 YBI 的人来说,愤怒、抑郁和焦虑往往会随着时间的推移而减少。对参与者进行的定性访谈表明,他们对 YBI 的总体满意度很高,并提供了与设施相关的上课障碍方面的信息。结论:尽管我们在这项研究中没有达到所有的可行性目标,但我们注意到参与者的热情很高。因此,我们认为这一研究方向值得继续进行,并将进一步关注如何减少与设施相关的上课和个人练习障碍。临床试验注册:NCT05336123.
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pilot Randomized Controlled Trial of a Yoga-Based Intervention Targeting Anger Management for People Who Are Incarcerated.

Introduction: Incarceration represents an opportune moment to improve self-management of anger and aggression. A hatha yoga-based intervention (YBI) could serve as a useful adjunctive intervention for anger within prisons. Methods: We enrolled 40 people with elevated levels of anger who were incarcerated (20 in a women's facility, and 20 in a men's facility) in a 10-week pilot randomized controlled trial of a YBI versus. a health education (HE) control group. Participants attended their respective groups once per week. We examined indices of feasibility and acceptability, including intervention credibility, expectancy the intervention would be helpful, intervention satisfaction, class attendance, engagement in personal practice, instructor fidelity, intervention safety, and study recruitment and retention rates. We also examined changes in clinical outcomes including anger, depression, anxiety, and behavioral infractions over time. Results: We met targets for several outcomes: credibility of the YBI and HE interventions, expectancy that they would be helpful, and satisfaction with the programs. Instructors demonstrated fidelity to both manuals. There were no serious adverse events related to study participation. Class attendance did not meet our target outcome in either facility and rates of personal practice met our target outcome in the men's but not the women's facility. For people enrolled in the YBI, anger, depression, and anxiety tended to decrease over time. Qualitative interviews with participants pointed to overall high satisfaction with the YBI and provided information on facility-related barriers to class attendance. Conclusion: Although we did not meet all our feasibility targets in this study, we note high participant enthusiasm. Thus, we believe this line of research is worth pursuing, with further attention to ways to decrease facility-related barriers to class attendance and personal practice. Clinical trials registration: NCT05336123.

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