Chronic fatigue syndrome treated by the traditional Chinese proce-dure abdominal tuina:a randomized controlled clinical trial
Chronic fatigue syndrome treated by the traditional Chinese procedure abdominal tuina: a randomized controlled clinical trial作者机构:Department of TuinaFirst Teaching Hospital of TianjinUniversity of Traditional Chinese MedicineTianjin 300193ChinaLaboratory for Biological Effects of TuinaState Administration of Traditional Chinese MedicineTianjin 300193China Department of TuinaFirst Teaching Hospital of Tianjin University of Traditional Chinese MedicineTianjin300193China University of Traditional Chinese MedicineTianjin 300193China Department of RespirationThe Affiliated Hospitalof Tianjin Academy of Traditional Chinese MedicineTianjin 300120China
出 版 物:《Journal of Traditional Chinese Medicine》 (中医杂志(英文版))
年 卷 期:2017年第37卷第6期
页 面:819-826页
核心收录:
学科分类:1005[医学-中医学] 100512[医学-针灸推拿学] 10[医学]
基 金:Supported by the National Natural Science Foundation:Use of the BDNF-CREB-Bcl-2 Protein Pathway to Investigate the Mechanism of Abdominal Tuina to Promote CFS Hippocampal Neuronal Remodeling(No.81360567) Based on the ENS-ICC-SMC Network to Investigate Abdominal Massage to Control the Intestinal Motility(No.81373762)
主 题:Tui Na Acupuncture Fatigue syndrome,chronic Randomized controlled trial Fatiguescale-14 Self-rating anxiety scale Hamilton ratingscale for depression
摘 要:OBJECTIVE: To evaluate the effect of the traditional Chinese procedure abdominal Tuina(AT) on chronic fatigue syndrome(CFS).METHODS: This randomized, single assessor-blinded clinical trial was carried out from May 2014 to April 2015. Eighty participants in the trial were divided randomly into two groups: experimental group and control. The experimental group(40 cases) was treated by AT and the control group(40 cases) by acupuncture. Each treatment was conducted once a day, 5 d for one course, at an interval of 2 d between each course. The whole treatment course lasted for 4 weeks. To ascertain the effect of AT and acupuncture, Fatigue Scale-14(FS-14), Self-rating Anxiety Scale(SAS) and Hamilton Rating Scale for Depression(HAMD) scores were used before and after treatment. Patients were followed up for3 months after ***: After treatment for 4 weeks, 77 patients(39 cases in the experimental group and 38 cases in the control group) completed the trial. The FS-14,SAS and HAMD scores decreased(P 0.05) significantly compared with those before treatment in both groups. The FS-14 and HAMD(P 0.05) scores in the experimental group were much lower than those in the control group. The difference in SAS scores between the two groups was not *** the final follow-up, CFS in two cases in the experimental group and three in the control group recurred, but the difference was not significant. The scores for the FS-14, SAS and HAMD in the experimental group were superior to those of the control group, and the difference was significant(P 0.05).No serious adverse events and few adverse events were ***: AT elicited a more efficacious effect than acupuncture alone on CFS.