Shi-style cervical manipulations for cervical radiculopathy: A multicenter randomized-controlled clinical trial

被引:15
作者
Cui, Xue-jun [1 ]
Yao, Min [1 ]
Ye, Xiu-lan [1 ]
Wang, Ping [2 ]
Zhong, Wei-hong [3 ]
Zhang, Rui-chun [4 ]
Li, Hui-ying [5 ]
Hu, Zhi-jun [1 ]
Tang, Zhan-ying [1 ]
Wang, Wei-min [2 ]
Qiao, Wei-ping [5 ]
Sun, Yue-li [1 ]
Li, Jun [1 ]
Gao, Yang [1 ]
Shi, Qi [1 ]
Wang, Yongjun [1 ]
机构
[1] Shanghai Univ Tradit Chinese Med, Longhua Hosp, Shanghai 200032, Peoples R China
[2] Tianjin Univ Tradit Chinese Med, Teaching Hosp 1, Tianjin, Peoples R China
[3] Fujian Univ Tradit Chinese Med, Rehabilitat Hosp, Fuzhou, Fujian, Peoples R China
[4] Xinjiang Uygur Autonomous Region Hosp Tradit Chin, Urumqi, Peoples R China
[5] Henan Univ Tradit Chinese Med, Affiliated Hosp 1, Zhengzhou, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
cervical radiculopathy; manipulations; randomized-controlled clinical trial; traction; MECHANICAL NECK PAIN; DISABILITY INDEX; THRUST MANIPULATION; MANUAL THERAPY; CASE SERIES; TRACTION; MOBILIZATION; EPIDEMIOLOGY; EXERCISE;
D O I
10.1097/MD.0000000000007276
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: There is a lack of high-quality evidence supporting the use of manipulation therapy for patients with cervical radiculopathy (CR). This study aimed to evaluate the effectiveness of Shi-style cervical manipulations (SCMs) versus mechanical cervical traction (MCT) for CR. Methods: This was a randomized, open-label, controlled trial carried out at 5 hospitals in patients with CR for at least 2 weeks and neck pain. The patients received 6 treatments of SCM (n=179) or MCT (n=180) over 2 weeks. The primary outcome was participant-rated disability (neck disability index), measured 2 weeks after randomization. The secondary outcomes were participant-rated pain (visual analog scale) and health-related quality of life (36-Item Short Form Health Survey [SF-36]). Assessments were performed before, during, and after (2, 4, 12, and 24 weeks) intervention. Results: After 2 weeks of treatment, the SCM group showed a greater improvement in participant-rated disability compared with the control group (P=.018). The SCM group reported less disability compared with the control group (P<.001) during the 26-week follow-up. The difference was particularly important at 6 months (mean -28.91 +/- 16.43, P<.001). Significant improvements in SF-36 were noted in both groups after 2 weeks of treatment, but there were no differences between the 2 groups. Conclusion: SCM could be a better option than MCT for the treatment of CR-related pain and disability.
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页数:7
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