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首页> 外文期刊>The American journal of Chinese medicine >External qigong for chronic pain.
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External qigong for chronic pain.

机译:外用气功用于慢性疼痛。

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摘要

External qigong as a pharmacotherapy adjunct was investigated in 50 subjects with chronic pain (pain lasting > 3 months with pain score of > or = 3 on 0-10 numeric analog scale) who presented to a qigong healing center. Participants were randomized to receive either external qigong treatment (EQT) or equivalent attention time (EAT) in weekly 30-min sessions for four consecutive weeks. Outcomes were assessed before and after sessions. The primary outcome measure was intensity of pain by a 10-cm visual analog scale used to rate all pain severity measurements. At 8-week follow-up, participants were contacted by telephone and mailed a questionnaire. Most had experienced pain for > 5 years (66%); the rest, for > 3 to 5 years (8%), 1 to 3 years (10%), or < 1 year but > 3 months (10%). The most frequent concomitant diagnoses were multifactorial (26%), osteoarthritis (18%), and low back pain (12%). Most patients were also receiving other treatments (74%); none previously had EQT. Participants were randomly assigned to EQT (n = 26) or EAT (n = 24). These groups had no significant differences at baseline except for prior awareness of qigong (EQT 31% vs. EAT 63%; p = 0.025). Compared to the EAT group, EQT participants had a significant decrease in pain intensity in the 2nd (p = 0.003), 3rd (p < 0.001), and 4th weeks of treatment (p = 0.003). At week 8, these differences in overall decreased pain intensity persisted but were not statistically significant.
机译:外部气功作为药物治疗的辅助手段,对50名慢性气喘病患者进行了研究(疼痛持续时间大于3个月,疼痛评分在0到10的模拟评分中大于或等于3),并呈递给气功康复中心。参与者被随机分配为在连续四周的每周30分钟内接受外部气功治疗(EQT)或等效的注意时间(EAT)。在会议之前和之后评估结果。主要结果指标是通过10厘米视觉模拟量表对疼痛强度进行评分,以评估所有疼痛严重程度。在8周的随访中,通过电话与参与者联系并寄出了调查表。大多数人经历了超过5年的疼痛(66%);其余时间为> 3至5年(8%),1至3年(10%)或<1年但大于3个月(10%)。最常见的伴随诊断是多因素(26%),骨关节炎(18%)和腰痛(12%)。大多数患者也接受其他治疗(74%);以前都没有EQT。参与者被随机分配到EQT(n = 26)或EAT(n = 24)。除了对气功的事先了解外,这些组在基线时无显着差异(EQT 31%对EAT 63%; p = 0.025)。与EAT组相比,EQT参与者在治疗的第2周(p = 0.003),第3周(p <0.001)和第4周(p = 0.003)疼痛强度显着降低。在第8周时,总体疼痛强度降低方面的差异持续存在,但无统计学意义。

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