Moxibustion Combined With Characteristic Lifestyle Intervention of Traditional Chinese Medicine in the Treatment of Abdominal Obesity: A Study Protocol for a Randomized Controlled Trial

Sponsor
Hubei Hospital of Traditional Chinese Medicine (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04501198
Collaborator
Shanxi Provincial Hospital of Traditional Chinese Medicine (Other), Shenzhen Bao'an Traditional Chinese Medicine Hospital Group (Other), Wuhan Hospital of Traditional Chinese and Western Medicine (Other), Xiangyang Hospital of Traditional Chinese Medicine (Other)
150
3
16

Study Details

Study Description

Brief Summary

This study will investigate whether the combination of moxibustion and characteristic lifestyle intervention of TCM can alleviate the clinical symptoms and improve quality of life and mental health in patients with abdominal obesity. The results are expected to provide clinical evidence for the application of the combination of moxibustion and characteristic lifestyle intervention of TCM in patients with abdominal obesity.

Condition or Disease Intervention/Treatment Phase
  • Device: moxibustion combined with characteristic lifestyle intervention of traditional chinese medicine
  • Device: Moxibustion combined with lifestyle intervention.
  • Device: lifestyle intervention
N/A

Detailed Description

This study will be a randomized controlled trial conducted from January, 2020 to January, 2022 that includes 150 participants who have abdominal obesity and meet the eligibility criteria. The participants will be randomly divided into 3 groups in a 2:2:1 allocation ratio.The intervention group will receive moxibustion combined with characteristic lifestyle intervention of TCM;the other group will receive moxibustion combined with lifestyle intervention;the control group will receive lifestyle intervention only.Each treatment will last 12 weeks including 8 weeks of intervention period and 4 weeks of follow-up period. The primary outcome is the waist circumference(WC),the secondary outcomes include obesity-related indicators,serum biochemical indexs,blood pressure, conversion score of constitution characteristics, and measurement of the scale.Adverse events will be recorded during the intervention and follow-up period.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
150 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Moxibustion Combined With Characteristic Lifestyle Intervention of Traditional Chinese Medicine in the Treatment of Abdominal Obesity: A Study Protocol for a Randomized Controlled Trial
Anticipated Study Start Date :
Sep 1, 2020
Anticipated Primary Completion Date :
Jan 1, 2021
Anticipated Study Completion Date :
Jan 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Moxibustion with characteristic lifestyle intervention of TCM

Participants will receive moxibustion combined with characteristic lifestyle intervention of traditional chinese medicine.In this study, xiusheng decoction, traditional exercises, and modern lifestyle intervention will be combined as the characteristic lifestyle intervention method of TCM to help participants establish healthy living habits. Participants will receive the treatment of moxibustion 6 times a week to fulfill a 8-session treatment course, and the intervention of Xiusheng Decoction and Traditional exercises will last for 8 weeks.While the intervention of modern lifestyle intervention will be conducted for 12 weeks including the treatment period of 8 weeks and the follow-up period of 4 weeks.

Device: moxibustion combined with characteristic lifestyle intervention of traditional chinese medicine
The moxibustion acupoints will be selected as①zhongwan, guanyuan, shenque, and zusanli;②pishu,shenshu. Acupoints group①will be selected on Monday, Wednesday, and Friday, Acupoints group②will be selected on Tuesday, Thursday, Saturday.Moxibustion treatment will be applied once every day, 6 times per week, for 8 consecutive weeks. Xiusheng decoction, traditional exercises, and modern lifestyle intervention will be combined as the characteristic lifestyle intervention method of TCM to help participants establish healthy living habits. The Xiusheng Decoction should be taken twice a day. Traditional exercises will be taken for 35~40 minutes everyday, 7 times a week. The intervention of Xiusheng Decoction and traditional exercises will be conducted for 8 weeks. All patients will be instructed to follow a good living habits which will last 12 weeks including the treatment period of 8 weeks and the follow-up period of 4 weeks.

Experimental: moxibustion with lifestyle intervention

Participants will receive moxibustion combined with lifestyle intervention. Participants will receive the treatment of moxibustion 6 times a week to fulfill a 8-session treatment course,while the intervention of modern lifestyle intervention will be conducted for 12 weeks including the treatment period of 8 weeks and the follow-up period of 4 weeks.

Device: Moxibustion combined with lifestyle intervention.
The moxibustion acupoints will be selected as①zhongwan, guanyuan, shenque, and zusanli;②pishu,shenshu. Acupoints group①will be selected on Monday, Wednesday, and Friday, Acupoints group②will be selected on Tuesday, Thursday, Saturday.Moxibustion treatment will be applied once every day, 6 times per week, for 8 consecutive weeks. All patients will be instructed to follow a good living habits including diet and exercise intervention which will last 12 weeks including the treatment period of 8 weeks and the follow-up period of 4 weeks.

Other: lifestyle intervention

Participants will receive lifestyle intervention which includes modern dietary exercise modifications. Participants will receive this treatment for a 8-session treatment course and 4-session follow-up course.

Device: lifestyle intervention
All patients will be instructed to follow a good living habits including diet and exercise intervention which will last 12 weeks including the treatment period of 8 weeks and the follow-up period of 4 weeks.

Outcome Measures

Primary Outcome Measures

  1. Changes in waistline [week 0,week 2,week 4,week 6,week 8,week 12]

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

Secondary Outcome Measures

  1. Changes in weight [week 0,week 2,week 4,week 6,week 8,week 12]

    Body weight will be measured by a body composition analyzer (OMRON V.BODY).

  2. Changes in body mass index [week 0,week 2,week 4,week 6,week 8,week 12]

    Body Mass Index is a simple calculation using a person's height and weight. The formula is BMI = kg/m2 where kg is a person's weight in kilograms and m2 is their height in metres squared.

  3. Changes in body fat percentage [week 0,week 2,week 4,week 6,week 8,week 12]

    The body fat percentage (BFP) of a human or other living being is the total mass of fat divided by total body mass, multiplied by 100. Body fat percentage will be measured by a body composition analyzer (OMRON V.BODY).

  4. Changes in basal metabolic value [week 0,week 2,week 4,week 6,week 8,week 12]

    Basal metabolic value will be measured by a body composition analyzer (OMRON V.BODY).

  5. Changes in hip circumference [week 0,week 2,week 4,week 6,week 8,week 12]

    hip circumference will be measured at the level of maximum posterior extension of the buttocks.

  6. Changes in waist-to-hip circumference ratio [week 0,week 2,week 4,week 6,week 8,week 12]

    waist-to-hip ratio is the dimensionless ratio of the circumference of the waist to that of the hips. This is calculated as waist measurement divided by hip measurement ( W ÷ H ).

  7. Changes in fasting blood-glucose [week 0, week 8]

    examined with the blood sample

  8. Changes in fasting insulin [week 0, week 8]

    examined with the blood sample

  9. Changes in insulin resistance index insulin resistance index insulin resistance index [week 0, week 8]

    examined with the blood sample

  10. Changes in total cholesterol [week 0, week 8]

    examined with the blood sample

  11. Changes in triglyceride [week 0, week 8]

    examined with the blood sample

  12. Changes in low density lipoprotein [week 0, week 8]

    examined with the blood sample

  13. Changes in high-density lipoprotein [week 0, week 8]

    examined with the blood sample

  14. Changes in uric acid [week 0, week 8]

    examined with the blood sample

  15. Changes in blood pressure [week 0, week 8]

    Both Systolic and diastolic blood pressure assessed by office and ambulatory blood pressure monitoring(mmHg).

  16. Changes in Conversion score of constitution characteristics [week 0, week 8, week 12]

    The scale classification of the patient's constitution according to Traditional Chinese Medicine theory into nine constitutions. The Constitution in Chinese Medicine Questionnaire (CCMQ) consists of 60 items to classify a person into one or more of nine body constitution types: balanced (8 Items), Qi-deficiency (8 Items), Yang-deficiency (7 Items), Yin-deficiency (8 Items), phlegm-wetness (8 Items), wetness-heat (6 Items), blood-stasis (7 Items), Qi-depression (7 Items), and special diathesis (7 Items). A higher score in the CCMQ scale indicates a higher likelihood of the specific body constitution. The original score is sum up each item's score. The conversion score of constitution characteristics is [(original scores- items)/(items*40]*100. The balanced constitution is the converted score >60 and the rest constitutions' converted scores all < 30. The unbalanced constitution is the converted score ≥40.

  17. Changes in the IWQOL - Lite scale score [week 0, week 8, week 12]

    Quality of life was examined using the Impact of Weight on Quality of Life (IWQOL) Kids questionnaire, which has a score range from 0(worst) to 100(best).

  18. Changes in the Emotional and Psychological Assessment scale [week 0, week 8, week 12]

    10 item self-report measure of psychological distress with five response categories (none of the time, a little of the time, some of the time, most of the time, all of the time). Scores range from 10 to 50; a higher score indicates more psychological distress.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 55 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
Patients recruited for this study should meet the following inclusion criteria:

1.Satisfying the criteria for the diagnosis of abdominal obesity; 2.18 years old≤age≤55 years old; 3.Being able to fully understand and voluntarily sign informed consent.

Exclusion Criteria:
Patients with any of the following criteria will be excluded from the study:
  1. Presence of endocrine disorders such as: polycystic ovary syndrome; Cushing's syndrome; uncorrected thyroid disease.

  2. Presence of diabetes mellitus, or hypertension, or abnormal liver and kidney functions, or mental diseases.

  3. Pregnant or lactating state, women who plan to become pregnant within 12 weeks.

  4. History of bulimia, anorexia, or any other eating disorders.

  5. Use of medications in the past 3 months, such as diet drugs, corticosteroids, antidepressants, which may affect weight or appetite.

  6. History of surgical weight loss, postoperative adhesions.

  7. History of participating in a clinical study of weight loss or any other therapies to lose weight in the past 3 months.

  8. Presence of local skin rupture, allergy and scar constitution.

  9. Unable to cooperate with the research caused by other diseases or reasons.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Hubei Hospital of Traditional Chinese Medicine
  • Shanxi Provincial Hospital of Traditional Chinese Medicine
  • Shenzhen Bao'an Traditional Chinese Medicine Hospital Group
  • Wuhan Hospital of Traditional Chinese and Western Medicine
  • Xiangyang Hospital of Traditional Chinese Medicine

Investigators

  • Principal Investigator: Zhongyu Zhou, Professor, Hubei Hospital of Traditional Chinese Medicine

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

Responsible Party:
Wang Jian, professor, Hubei Hospital of Traditional Chinese Medicine
ClinicalTrials.gov Identifier:
NCT04501198
Other Study ID Numbers:
  • 202006009
First Posted:
Aug 6, 2020
Last Update Posted:
Sep 16, 2020
Last Verified:
Sep 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Wang Jian, professor, Hubei Hospital of Traditional Chinese Medicine
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 16, 2020