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Day-to-day changes of auricular point acupressure to manage chronic low back pain : a 29-day randomized controlled study

机译:耳穴穴位按摩的每日变化以控制慢性下腰痛:一项为期29天的随机对照研究

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摘要

Objective: The purpose of this study was to determine the effects of a 4-week auricular point acupressure (APA) treatment on chronic low back pain (CLBP) outcomes and examine the day-to-day variability of CLBP in individuals receiving APA for CLBP over 29 days. Design: This was a prospective, randomized controlled trial (RCT). Data were collected at baseline, during each of the four office visits for APA treatment, after the completion of the 4-week intervention, and 1 month after the last treatment. A daily diary was given to each participant to record his or her APA practices, analgesic use, and pain intensity. Interventions: APA was used to manage CLBP. The participants received one APA treatment per week for 4 weeks. Patients and Setting. Sixty-one participants with CLBP were randomized into either a real APA or sham APA treatment group. Participants were recruited from primary care offices and clinics or through the Research Participant Registry at the University of Pittsburgh. Results: Among participants in the real APA group, a 30% reduction of worst pain was exhibited after the first day of APA treatment, and continuous reduction in pain (44%) was reported by the completion of the 4-week APA. This magnitude of pain reduction reached the clinically significant level of improvement reported in other clinical trials of chronic pain therapies. Analgesic use by participants in the real APA group also was reduced compared with use by participants in the sham group. Conclusion: This study shows that APA is a promising pain management strategy that is not invasive and can be self-managed by participants for CLBP. Given the day-to-day fluctuation in ratings, the tighter ecologic assessment of pain scores and other treatment parameters are an important pragmatic aspect of the design of chronic pain studies.
机译:目的:本研究的目的是确定为期4周的耳穴指压(APA)治疗对慢性腰背痛(CLBP)结局的影响,并检查接受APA接受CLBP的个体的CLBP的每日变化超过29天。设计:这是一项前瞻性随机对照试验(RCT)。在为期4周的干预完成后以及在最后一次治疗后的1个月内,在进行APA治疗的四个办公室就诊期间,均在基线时收集了数据。每天给每位参与者提供日记,以记录他或她的APA做法,止痛药的使用和疼痛强度。干预措施:APA用于管理CLBP。参与者每周接受一种APA治疗,持续4周。患者和环境。将61名CLBP参与者随机分为真正的APA或假APA治疗组。参与者是从初级保健办公室和诊所或通过匹兹堡大学的研究参与者注册处招募的。结果:在真正的APA组中,在APA治疗的第一天后,最严重疼痛减轻了30%,并且在完成4周的APA后,疼痛持续减轻(44%)。在慢性疼痛疗法的其他临床试验中,这种减轻疼痛的程度达到了临床上显着的改善水平。与假手术组的参与者相比,真正的APA组的参与者使用的止痛药也有所减少。结论:这项研究表明,APA是一种有前途的疼痛管理策略,该方法无创且可由CLBP参与者自我管理。考虑到评分的日常波动,对疼痛评分和其他治疗参数的更严格的生态学评估是设计慢性疼痛研究的一个重要的务实方面。

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