老年慢性背痛人群实施气功锻炼的可行性研究

N. Guillaume
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引用次数: 0

摘要

背景:慢性背痛(CBP)是困扰求医老年人的常见症状。缓解这种情况的最常见的策略是药理学,并引起有害的副作用。益人医学气功(YRMQ)已经证明,只需一次这种温和的锻炼就可以减轻老年人的慢性疼痛。本临床试验的目的是评估气疗法在减轻疼痛或不适方面的有效性。方法:本初步研究评估了YRMQ在7名CBP患者中的应用。年龄为66.7+/-3.4岁的CBP患者除了每周在家练习两次较短的气功练习外,还参加了每周一小时的团体气功练习。使用视觉模拟评分(VAS)评估疼痛强度,显示症状减轻。其他评估工具如罗兰莫里斯残疾问卷(RMDQ)和简短疼痛量表(BPI)被用来测量在5周的试验过程中的疼痛减轻。结果:7名受试者(女4名,男3名)成功入组。在7名参与者中,28.6%(2名)的受试者每周都来,42.8%(3名)缺席一周,28.6%(2名)缺席两周或两周以上。使用VAS调整后的平均低背部强度开始于4.43+/-2.76,结束于3.16+/-2.4 (P=0.144)。用RMDQ测量生活质量,从试验开始时的6.43+/-5.65到结束时的4+/-4.24 (P=0.042)有所下降。最后,两部分BPI也分别从基线(第一部分和第二部分)从4.61+/-2.82下降到2.65+/-0.91 (P=0.043),从4.25+/-2.74下降到2.23+/-1.29 (P=0.043)。没有发现严重或危及生命的不良反应。结论:气功已被证明至少在短期内可以减轻疼痛和止痛药的使用。我们的初步疗效结果与之前的气功研究一致,表明通过评估评分的改变可以改善背部疼痛,但没有足够的显著的统计证据来证明所提出的练习的可复制疗效。我们的试验仍然存在许多局限性,例如研究组没有对照组来比较结果。与我们的试点设计相关的小样本量限制了我们的统计能力。对患有CBP的老年人群样本进行为期5周的气功练习试点试验是适度可行的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Feasibility Study on the Implementation of Qigong Exercises in the Elderly Population Suffering from Chronic Back Pain
Background: Chronic Back Pain (CBP) is a common symptom bothering the elderly population seeking medical care. The most common strategy suggested for the relief of this condition is pharmacological and causes harmful side effects. Yi Ren Medical Qigong (YRMQ) has demonstrated that just one single application of this gentle exercise could reduce chronic pain in elderly people. The objective of this clinical trial was to evaluate the effectiveness of qi therapy in decreasing pain or discomfort. Methods: This pilot study evaluated the use of YRMQ in a group of seven participants with CBP. Participants aged 66.7+/-3.4 years with CBP took part in weekly one-h group qigong sessions in addition to practicing a shorter version of the exercises at home twice a week. Pain intensity was evaluated using a Visual Analog Scale (VAS), showing reduction of symptoms. Other assessment tools such as the Roland Morris Disability Questionnaire (RMDQ) and the Brief Pain Inventory (BPI) scales were used to measure the pain reduction over the course of the 5-week trial. Results: A total of 7 subjects (4 women and 3 men) were enrolled successfully in the trial. Out of the seven participants, 28.6% (two) of the subjects came every week, 42.8% (three) missed one week, while 28.6% (two) missed two or more weeks. The mean adjusted low back intensity using the VAS started at 4.43+/-2.76 and ended at 3.16+/-2.4 (P=0.144). The quality of life was measured with the RMDQ and showed a reduction from the beginning of the trial at 6.43+/-5.65 to the end at 4+/-4.24 (P=0.042). Finally the two-part BPI also decreased from the baseline to week-5 respectively (Part I and II) from 4.61+/-2.82 to 2.65+/-0.91 (P=0.043) and from 4.25+/-2.74 to the end at 2.23+/-1.29 (P=0.043). No serious or life-threatening adverse effects were found. Conclusion: Qigong has proven to provide at least in the short term some reduction of pain and pain medication use. Our preliminary efficacy results were consistent with previous qigong studies showing improvement of back pain via assessment score changes, but not enough significant statistical evidence relevant to prove replicable efficacy of the proposed exercises. There were still multiple limitations to our trial such as the study group not having a control group to compare the results. The small sample size associated with our pilot design limited our statistical power. Conducting a 5 week pilot trial of qigong exercises for an elderly population sample with CBP was moderately feasible.
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