Acupuncture for obesity:study protocol for a randomised controlled trial.
Study Goal
The researchers aimed to evaluate the efficacy and safety of acupuncture for treating obesity through a randomized, sham-controlled trial.
Results Summary
The study is ongoing, so no results are reported in the abstract. Outcomes will include changes in body weight, BMI, waist circumference, body fat percentage, blood pressure, metabolic markers, and psychological/social functions.
Population
160 eligible participants with obesity.
Effective Dosage
Three times a week for 12 weeks.
Duration
12 weeks of intervention, with a 16-week follow-up.
Interactions
None mentioned
| Intervention | Direction | Endpoint | Population | Dosage | Impact | Claim # |
|---|---|---|---|---|---|---|
acupuncture | neutral | treating obesity | participants with obesity | - | evaluate the efficacy and safety | #1 |
verum acupuncture | neutral | percentage change in body weight | participants with obesity | - | will be evaluated | #2 |
verum acupuncture | neutral | body mass index (BMI) | participants with obesity | - | will be evaluated | #3 |
verum acupuncture | neutral | waist circumference (WC) | participants with obesity | - | will be evaluated | #4 |
verum acupuncture | neutral | body fat percentage (BF%) | participants with obesity | - | will be evaluated | #5 |
verum acupuncture | neutral | blood pressure | participants with obesity | - | will be evaluated | #6 |
verum acupuncture | neutral | fasting blood glucose | participants with obesity | - | will be evaluated | #7 |
verum acupuncture | neutral | insulin | participants with obesity | - | will be evaluated | #8 |
verum acupuncture | neutral | glycosylated haemoglobin A1c | participants with obesity | - | will be evaluated | #9 |
verum acupuncture | neutral | blood lipids | participants with obesity | - | will be evaluated | #10 |
verum acupuncture | neutral | physical functioning score on the Short Form 36 Health Survey | participants with obesity | - | will be evaluated | #11 |
verum acupuncture | neutral | psychological and social functions | participants with obesity | - | will be evaluated | #12 |
verum acupuncture | neutral | body image scale | participants with obesity | - | will be evaluated | #13 |
verum acupuncture | neutral | psychological function scale | participants with obesity | - | will be evaluated | #14 |
verum acupuncture | neutral | social function scale of the BODY-Q | participants with obesity | - | will be evaluated | #15 |
verum acupuncture | neutral | Rosenberg Self-Esteem Scale | participants with obesity | - | will be evaluated | #16 |
verum acupuncture | neutral | Patient Health Questionnaire-9 | participants with obesity | - | will be evaluated | #17 |
verum acupuncture | neutral | Dutch Eating Behaviour Questionnaire | participants with obesity | - | will be evaluated | #18 |
BACKGROUND: Obesity 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 ANALYSIS: A 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 DISSEMINATION: Ethical 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 NUMBER: Chinese Clinical Trial Registry (ChiCTR2200062092).