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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
来源:
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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