Acupuncture treatment for knee osteoarthritis with sensitive points: protocol for a multicentre randomised controlled trial. Issue 10 (2nd October 2018)

• Record Type: Journal Article
• Authors: Tang, Li; Jia, Pengli; Zhao, Ling; Kang, Deying; Luo, Yanan; Liu, Jiali; Li, Ling; Zheng, Hui; Li, Ying; Li, Ning; Guyatt, Gordon; Sun, Xin
• Is Part Of: BMJ open. Volume 8:Issue 10(2018)
• Publication Date: 2018-10-02
• Subjects: acupuncture -- knee osteoarthritis -- randomised controlled trial -- sensitised points; Medicine -- Research -- Periodicals; 610.72
• DOI: 10.1136/bmjopen-2018-023838
• Languages: English
• ISSNs: 2044-6055

Abstract

Abstract : Introduction: There is a lack of curative medical treatment for patients with knee osteoarthritis (KOA). Acupuncture represents an important alternative therapy. According to the theory of traditional Chinese medicine and preliminary clinical evidence, the patients' acupoints and tender points may become sensitised when the body suffers from a disease state; stimulation of such sensitive points could lead to a disease improvement. It is thus hypothesised that acupuncture at highly sensitised points on patients with KOA would achieve better treatment outcomes than acupuncture at low/non-sensitised points. Previously, we conducted a pilot trial to prove the feasibility of further investigation. Methods and analysis: A three-arm, parallel, multicentre randomised controlled trial of 666 patients will be conducted at four hospitals of China. Eligible patients with KOA who consent to participate will be randomly assigned to a high-sensitisation group (patients receive acupuncture treatment at high-sensitive points), a low/non-sensitisation group (patients receive acupuncture treatment at low/non-sensitive points) or a waiting-list group (patients receive standard acupuncture treatment after the study is concluded) via a central randomisation system using 1:1:1 ratio. The primary outcome is the change of Western Ontario and McMaster Universities Osteoarthritis Index total score from baseline to 16 weeks. Outcome assessors and data analysts will be blinded and participants will be asked not to reveal their allocation to assessors. The outcome analyses will be performed both on the intention-to-treat and per-protocol population. The primary analyses will test if acupuncture at highly sensitised points would achieve statistically better treatment outcomes than acupuncture at low/non-sensitised points and no acupuncture (ie, waiting list), respectively. A small number of prespecified subgroup analyses will be conducted. Ethics and dissemination: Ethics approval has been granted by the Bioethics Subcommittee of West China Hospital, Sichuan University: 2017 (Number 228). Results will be expected to be published in peer-reviewed journals. Trial registration number: NCT03299439 .