Manual acupuncture versus sham acupuncture and usual care for the prevention of primary dysmenorrhea (PD): study protocol for a randomized controlled trial

被引:5
作者
Yu, Lingling [1 ]
Liu, Shiqin [1 ]
Zheng, Cuihong [1 ]
Liu, Wenhua [1 ]
Wang, Hua [2 ]
Liang, Fengxia [2 ]
Lu, Wei [2 ]
Xu, Shabei [1 ]
Wang, Wei [1 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Hosp, Tongji Med Coll, 1095 Jiefang Ave, Wuhan 430030, Hubei, Peoples R China
[2] Hubei Univ Chinese Med, Acupuncture & Moxibust Inst, Coll Acupuncture & Moxibust, Hubei Prov Collaborat Innovat Ctr Prevent Treatme, 1 Tanhualin Rd, Wuhan 430030, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Primary dysmenorrhea; Manual acupuncture; Efficacy; Safety; Clinical trial; Study protocol; CHRONIC PAIN; DEPRESSION; SCALE; ADOLESCENTS; RELIABILITY; PREVALENCE; VALIDATION; INVENTORY; MECHANISM; VALIDITY;
D O I
10.1186/s13063-020-04720-5
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
BackgroundPrimary dysmenorrhea (PD) is a leading cause of dysmenorrhea among adolescent girls. Manual acupuncture may be considered as an effective treatment for PD, but high-quality evidence remains limited. This trial aims to evaluate the efficacy and safety of acupuncture for the prevention of PD as compared with sham acupuncture and usual care.Methods/designThis is a three-arm, randomized, controlled clinical trial in which the patients, assessors, and statisticians will be blinded. A total of 300 acupuncture-naive patients who were diagnosed as PD will be randomly allocated to the verum acupuncture, sham acupuncture, or usual care groups in a 2:2:1 ratio. Patients in the verum acupuncture group will receive manual acupuncture at specific acupuncture points with penetrating needling, while those in the sham acupuncture group will receive non-penetrating needling at non-acupuncture points. They will be given five sessions over a menstrual cycle for 3 menstrual cycles. Patients in the usual care group will receive health education and informed to receive manual acupuncture for free after waiting for 7 menstrual cycles. The primary outcome will be the change from baseline in the Cox Menstrual Symptom Scale Score (CMSS). The secondary outcomes will be the changes in Massachusetts General Hospital Acupuncture Sensation Scale (MASS), visual analog scale (VAS), Short-Form McGill Pain Questionnaire 2 (SF-MPQ-2), Pittsburgh Sleep Quality Index (PSQI), Beck Anxiety Inventory (BAI), Beck Depression Inventory II (BDI- II), Acupuncture Expectancy Scale (AES), 60-item NEO Personality Inventory-Short Form (NEO-FFI), and acute medication intake. The adverse events will be recorded at every visit. The analyses will be performed base on a full analysis set (FAS) and a per-protocol set (PPS).DiscussionThis study may provide high-quality evidence regarding the efficacy and safety of manual acupuncture for PD. In addition, the results of this study will help to identify the efficacy of acupuncture due to the specific effects of acupuncture or placebo effects of acupuncture ritual.Trial registrationClinical Trials.gov NCT02783534. Registered on 26 May 2016
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页数:10
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