Acupuncture for obesity: study protocol for a randomised controlled trial

BackgroundObesity is a major public health issue in China and around the world. While acupuncture is often used in clinical practice, there is a lack of conclusive evidence for its weight-loss effect. Thus we will conduct a parallel, randomised, sham-controlled trial to evaluate the efficacy and saf...

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Veröffentlicht in:BMJ open 2024-08, Vol.14 (8), p.e083158
Hauptverfasser: Zhao, Xinyu, Wang, Yang, Li, Xiaoyi, Wu, Nianwei, Zhang, Shanshan, Wu, Shiyi, Hu, Peiqun, Chen, Ximei, Zhou, Lei, Wei, Aiming, Pan, Chongsheng, Liu, Yunlu, He, Benxiang, Hu, Yushi, Zhu, Tianmin, Pan, Xiong-Fei
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Sprache:eng
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Zusammenfassung:BackgroundObesity is a major public health issue in China and around the world. While acupuncture is often used in clinical practice, there is a lack of conclusive evidence for its weight-loss effect. Thus we will conduct a parallel, randomised, sham-controlled trial to evaluate the efficacy and safety of acupuncture for treating obesity.Methods and analysisA total of 160 eligible participants with obesity will be randomly assigned to the verum acupuncture group or sham acupuncture group at a ratio of 1:1. All participants will be treated three times a week for a duration of 12 weeks, and followed up for another 16 weeks. The primary outcome is the percentage change in body weight from baseline to Week 12. The secondary outcomes include body mass index (BMI), waist circumference (WC), body fat percentage (BF%), blood pressure, fasting blood glucose, insulin, glycosylated haemoglobin A1c, blood lipids, and physical functioning score on the Short Form 36 Health Survey. Other secondary outcomes including psychological and social functions will also be evaluated using the body image scale, psychological function scale, and social function scale of the BODY-Q, Rosenberg Self-Esteem Scale, Patient Health Questionnaire-9, and Dutch Eating Behaviour Questionnaire. BMI, WC, BF% and blood pressure will be evaluated at Week 0, 4, 8, 12 and 28. Other secondary outcomes will be measured at Week 0, 12 and 28, respectively. Adverse events will be recorded in detail during the trial.Ethics and disseminationEthical approval of this trial was granted by the Ethics Committee of Chengdu Sport University (2023–102). Written informed consent will be obtained from study participants before enrolment. The findings will be disseminated through peer-reviewed journals.Trial registration numberChinese Clinical Trial Registry (ChiCTR2200062092).
ISSN:2044-6055
2044-6055
DOI:10.1136/bmjopen-2023-083158