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Clinical Trials/NCT03815253
NCT03815253CompletedNot Applicable

Electro-acupuncture for Central Obesity: a Single Blinded Randomized Sham-controlled Clinical Trial

Hong Kong Baptist University1 site in 1 country168 target enrollmentStarted: February 1, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
168
Locations
1
Primary Endpoint
Changes in waist circumference

Study Overview

Brief Summary

In this study, a 8-week, single blinded, randomized controlled clinical trial will be conducted to examine the efficacy and safety of body acupuncture in the treatment of central obesity in Hong Kong.

Detailed Description

This is a pilot single-blind, randomized, sham-controlled trial. 168 central obesity patients will be randomly assigned to acupuncture group or control group. The duration of the treatment will be 8 weeks with 2 session per week and the follow-up period will be 2 weeks.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Masking Description

Subjects of both groups will be randomly assigned to receive either electro-acupuncture or control (sham) treatment. For randomization, simple, complete non-sequential random numbers will be generated in advance by a computer program in a block of four, and kept by the principal investigator. After a patient's eligibility is confirmed, a randomization number which corresponds to the group allocation will be provided to the acupuncturist by the PI. This arrangement will ensure that the clinical assessor and participants are blinded to the allocation.

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients who meet all of the following criteria are defined as eligible participants: men and women aged between 18 and 65 years old; BMI ≥ 25 kg/m2; central obesity, defined as WC of ≥ 90 cm in men and ≥ 80 cm in non-pregnant women according to ICD-10 [24]; not receiving any other weight control measures or any medical and/or drug history in last 3months.

Exclusion Criteria

  • •Patients who meet any of the following criteria should be excluded from the study: endocrine diseases, including thyroid disorder, pituitary disorder, sex gland disorder, etc.; heart diseases, including arrhythmia, heart failure, myocardial infarction, patients with pacemaker; allergy and immunology diseases; bleeding tendency; pregnant or lactating women; impaired hepatic or renal function; stroke or unable to exercise.

Arms & Interventions

Acupuncture group

Experimental

Body electro-acupuncture will be conducted for 2 sessions per week over 8 consecutive weeks.

Body electro-acupuncture will choose eight acupoints as Tianshu(ST-25), Daheng(SP-15), Daimai(GB-26), Qihai(CV-6), Zhongwan(CV-12), Zusanli (ST-36), Fenlong(ST-40), Sanyinjiao(SP-6).Disposable acupuncture needles (verum acupuncture needles asia-med Special No. 16 with 0.30 x 0.30mm matching the Streitberger sham-needles) will be inserted at a depth of 10-25 mm into the points.

We will also deliver electrical stimulation with dense-disperse waves with 50Hz at 10 volts through electrical acupuncture stimulation instrument (ES-160 6-Channel Programmable Electro-acupuncture) to the abdominal points. The bodily needles will be retained for 30 minutes.

Intervention: acupuncture (Other)

sham-acupuncture group

Placebo Comparator

As to the participants allocated to control group, Streitberger's non-invasive acupuncture needles (Gauge 8 x 1.2" / 0.30 x 30 mm) will be applied to act as sham control at the same acupoints with same stimulation modality. However, the needles will be only adhered to the skin instead of insertion. The validity and credibility of this model has been well demonstrated.

Intervention: acupuncture (Other)

Outcomes

Primary Outcomes

Changes in waist circumference

Time Frame: 0,1,2,3,4,5,6,7,8, 11, 15,18, 21, 24 weeks

Waist circumference will be measured around the abdomen at the level of the umbilicus (belly button).

Secondary Outcomes

  • Changes in hip circumference(0,1,2,3,4,5,6,7,8,9,11,15,18, 21, 24 weeks)
  • Adverse events after treatment and follow up(0,1,2,3,4,5,6,7,8, 15,18, 21, 24 weeks)
  • Changes in waist-to-hip circumference ratio(0,1,2,3,4,5,6,7,8, 15,18, 21, 24 weeks)
  • Changes in Body Mass Index(0,1,2,3,4,5,6,7,8, 15,18, 21, 24 weeks)
  • Changes in total cholesterol (TC), triglyceride (TG) and fasting blood glucose (FBG)(0, 8 weeks)
  • Changes in body fat percentage(0,1,2,3,4,5,6,7,8, 15,18, 21, 24 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Zhong Lidan

Research Assistant Professor

Hong Kong Baptist University

Study Sites (1)

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