Thread Embedding Acupuncture Therapy for Weight Loss

Not Applicable

Recruiting

• Conditions: Obesity and Overweight

• Registration Number: NCT06653530
• Lead Sponsor: Beijing Hospital of Traditional Chinese Medicine

Brief Summary

Obesity is the most prevalent chronic disease worldwide, affecting approximately 800 million adults. Excess adiposity and its numerous complications, including cardiovascular disease and type 2 diabetes, impose a considerable economic burden and constitute major contributors to global morbidity and mortality. Treatments that result in substantial weight reductions may improve outcomes for people living with obesity. Thread embedding acupuncture which provides long-term acupoints stimulation may be an effective treatment option for obesity. However, effects of thread embedding on obesity remain uncertain because of the small sample sizes or other methodological limitations. The objective of this multi-center, randomized, sham-controlled trial is to assess the effect of thread embedding acupuncture for alleviating weight.

Detailed Description

The present multi-center, randomized, sham-controlled, parallel-group trial aims to evaluate the effect of thread embedding acupuncture in patients with obesity.

The patients will be randomized to receive one of two treatment arms: thread embedding acupuncture and sham thread embedding acupuncture. The participants will receive treatment that consists of 18 thread embedding acupuncture or sham thread embedding acupuncture sessions over a 24-week period after baseline (once a week for the first 12 weeks and every two weeks for the next 12 weeks). At the end of 24 weeks treatment, the change of weight in overweight/obese participants between the two groups will be analyzed.

Study Timeline

• Status Verified: 2024-10
• Study First Submitted: 2024-10-21
• Study First Submitted QC: 2024-10-21
• Study First Posted: 2024-10-22
• Study Start: 2024-11-01
• Last Update Submitted: 2025-01-15
• Last Update Posted: 2025-01-16
• Primary Completion: 2026-10-31
• Study Completion: 2026-10-31

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 400

Inclusion Criteria

1. Body-mass index: a. BMI ≥ 28 kg/m2 or b. BMI ≥ 24 kg/m2 with the presence of at least one of the following weight-related complications (treated or untreated): diabetes, hypertension, lipid metabolism disorders, obstructive sleep apnea, cardiovascular disease, knee osteoarthritis, hyperuricemia, fatty liver;
2. Male or female, age between 18 and 75 years at the time of signing informed consent;
3. No history of receiving thread embedding treatment;
4. History of at least one self-reported unsuccessful dietary effort and exercise program to lose body weight;
5. Informed consent obtained.

Exclusion Criteria

1. A self-reported change in body weight ≥ 5 kg within 90 days before screening;
2. Treatment with any medication for the indication of obesity within the past 90 days before Screening;
3. Previous or planned (during the trial period) obesity treatment with surgery or a bodyweight loss device. However, the following were allowed: (1) liposuction and/or abdominoplasty, if performed more than 1 year before screening; (2) lap banding, if the band had been removed more than 1 year before screening; (3) intragastric balloon, if the balloon had been removed more than 1 year before screening; or (4) duodenal-jejunal bypass sleeve, if the sleeve had been removed more than 1 year before screening;
4. Have obesity induced by other endocrinologic disorders (for example, Cushing Syndrome) or diagnosed monogenetic or syndromic forms of obesity (for example, Melanocortin 4 Receptor deficiency or Prader Willi Syndrome);
5. Uncontrolled thyroid disease, defined as thyroid stimulating hormone (TSH)>6.0 mIU/L or <0.35 mIU/L as measured by the central laboratory at screening;
6. Diagnosed with type 2 diabetes mellitus ≤180 days prior to the day of screening or those who have taken treatment with oral agents that were unstable (different drug(s), dose, or dosing frequency) within the 90 days prior to screening;
7. Receipt of any acupuncture treatment for obesity within 90 days before screening;
8. Participation in any structured, monitored weight-loss program within 90 days before screening;
9. Active inflammatory bowel disease, celiac disease, chronic pancreatitis, or other disorder potentially causing malabsorption;
10. Any of the following severe cardiovascular diseases: myocardial infarction, stroke, heart failure, symptomatic peripheral vascular diseases, or hospitalization for unstable angina or transient ischemic attack within the last 6 months prior to screening;
11. History of malignant neoplasms within the past 5 years prior to screening. Basal and squamous cell skin cancer and any carcinoma in-situ are allowed;
12. Chronic respiratory, neurological, musculoskeletal or other disorders where, in the judgement of the investigator, participants would have unacceptable risk or difficulty in complying with the protocol;
13. Surgery scheduled for the duration of the trial, except for minor surgical procedures, in the opinion of the investigator;
14. Known or suspected abuse of alcohol or recreational drugs;
15. Female who was pregnant, breast-feeding, or intended to become pregnant, or was of child-bearing potential and not using a highly effective contraceptive method;
16. Known or suspected hypersensitivity to trial product or related products;
17. Participation in another clinical trial within 90 days before screening;
18. Any disorder, unwillingness, or inability, not covered by any of the other exclusion criteria, which in the investigator's opinion might have jeopardised the participant's safety or compliance with the protocol.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Relative change in body weight	From baseline (week 0) to end of treatment (week 24)	Measured in percentage (%)

Secondary Outcome Measures

Name	Time	Method
Body weight reduction greater than or equal to 5%	From baseline (week 0) to end of treatment (week 24)	Measured as the percentage of participants
Body weight reduction greater than or equal to 10%	From baseline (week 0) to end of treatment (week 24)	Measured as the percentage of participants
Change in body weight	From baseline (week 0) to end of treatment (week 24)	Measured in kilogram (kg)
Change in Body Mass Index (BMI)	From baseline (week 0) to end of treatment (week 24)	Measured in kilogram per square meter (kg/m\^2)
Change in body fat rate	From baseline (week 0) to end of treatment (week 24)	Measured in percentage points
Change in waist circumference	From baseline (week 0) to end of treatment (week 24)	Measured in centimeter (cm)
Change in waist-to-hip ratio	From baseline (week 0) to end of treatment (week 24)	Calculated by dividing the waist circumference(cm) by the hip circumference(cm).
Change in Systolic Blood Pressure (SBP)	From baseline (week 0) to end of treatment (week 24)	Measured in millimeter of mercury (mmHg)
Change in Diastolic Blood Pressure (DBP)	From baseline (week 0) to end of treatment (week 24)	Measured in mmHg
Change in Glycated Haemoglobin (HbA1c)	From baseline (week 0) to end of treatment (week 24)	Measured in percentage points
Change in Fasting Plasma Glucose (FPG)	From baseline (week 0) to end of treatment (week 24)	Measured as millimole per liter (mmol/L)
Change in fasting serum insulin	From baseline (week 0) to end of treatment (week 24)	Measured as milli-international units per milliliter (mIU/mL)\]
Change in high-density lipoprotein (HDL) cholesterol	From baseline (week 0) to end of treatment (week 24)	Measured as mmol/L
Change in low-density lipoprotein (LDL) cholesterol	From baseline (week 0) to end of treatment (week 24)	Measured as mmol/L
Change in triglycerides	From baseline (week 0) to end of treatment (week 24)	Measured as mmol/L
Change in total cholesterol	From baseline (week 0) to end of treatment (week 24)	Measured as mmol/L
Change in Short Form-36 (SF- 36) Physical Functioning score	From baseline (week 0) to end of treatment (week 24)	The SF-36 is a 36-item commonly used generic clinical outcome assessment instrument measuring health-related quality of life and general health status across disease areas. SF-36 questionnaire measures 8 domains of functional health and well-being as well as 2 component summary scores (physical component summary and mental component summary). This endpoint assesses the physical functioning domain.
Change in SF-36: Physical Component Summary Score	From baseline (week 0) to end of treatment (week 24)	The SF-36 is a 36-item commonly used generic clinical outcome assessment instrument measuring health-related quality of life and general health status across disease areas. SF-36 questionnaire measures 8 domains of functional health and well-being as well as 2 component summary scores (physical component summary and mental component summary).This endpoint assesses the physical component summary.
Change in SF-36: Mental Component Summary score	From baseline (week 0) to end of treatment (week 24)	The SF-36 is a 36-item commonly used generic clinical outcome assessment instrument measuring health-related quality of life and general health status across disease areas. SF-36 questionnaire measures 8 domains of functional health and well-being as well as 2 component summary scores (physical component summary and mental component summary). This endpoint assesses the mental component summary.

Trial Locations

Locations (1)

Beijing Hospital of Traditional Chinese Medicine; 🇨🇳 Beijing, Beijing, China