Efficacy of five-step shoulder manipulation for rotator cuff-related shoulder pain: protocol for a multicenter randomized controlled trial

被引:0
|
作者
Liu, Shuang [1 ,2 ]
Liu, Jin-Tao [3 ]
Chen, Lin [1 ]
Fan, Tian-You [1 ]
Cui, Xue-Jun [2 ]
Cheng, Shao-Dan [4 ]
Chen, Yan-Jiao [5 ]
Shi, Qi [2 ,6 ]
Xue, Chun-Chun [1 ]
Li, Xiao-Feng [1 ,6 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Shanghai Municipal Hosp Tradit Chinese Med, 274 Zhijiangzhong Rd, Shanghai 200071, Peoples R China
[2] LongHua Hosp Shanghai Univ Tradit Chinese Med, 725 Wanpingnan Rd, Shanghai 200032, Peoples R China
[3] Suzhou Hosp Tradit Chinese Med, 899 Wuzhongxi Rd, Suzhou 215009, Jiangsu, Peoples R China
[4] Shanghai GuangHua Hosp Integrated Tradit Chinese &, 540 Xinhua Rd, Shanghai 200052, Peoples R China
[5] YueYang Hosp Integrated Tradit Chinese & Western M, Shanghai Res Inst Acupuncture & Meridian, 650 Wanpingnan Rd, Shanghai 200030, Peoples R China
[6] Qi Shis Studio Famous Chinese Med Physician, 274 Zhijiangzhong Rd, Shanghai 200032, Peoples R China
关键词
Manipulation; Rotator cuff-related shoulder pain; Five-step shoulder manipulation; Exercises; Randomized controlled trials; PREVALENCE; REPAIR;
D O I
10.1186/s13063-023-07540-5
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
BackgroundRotator cuff-related shoulder pain (RCRSP) is the most common cause of shoulder disorders. In China, manipulation has been used extensively for the treatment of patients with RCRSP. However, high-quality clinical evidence to support the therapeutic effect of manipulation is still limited.MethodsA multicenter, participant-, outcome assessor-, and data analyst-blinded, randomized, placebo-controlled trial will be conducted. A total of 280 participants with RCRSP will be recruited from three hospitals and randomly assigned to a five-step shoulder manipulation (FSM) group or a sham manipulation (SM) group. Each group will receive four weekly treatment sessions, with all participants performing exercises at home for 12 weeks. Assessments, namely the Constant-Murley score, visual analog scale, range of motion, and 36-Item Short Form Survey, will be made at baseline, 4, 12, 18, and 24 weeks. Adverse events during the study will also be recorded.DiscussionThis is a pragmatic clinical trial to evaluate the efficacy and safety of FSM in patients with RCRSP. The findings of this study will provide worthy clinical evidence for manual therapy for RCRSP.
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页数:11
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