Intervention study to verify the effect of the changes in intestinal bacteria by intake of tea catechin and inulin on visceral fat reductio
- Conditions
- Visceral fat obese
- Registration Number
- JPRN-jRCTs021230004
- Lead Sponsor
- Mikami Tatsuya
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 114
Those who are participants in the 2023 Iwaki Health Promotion Project Medical Checkup and meet the following inclusion criteria.
-Inclusin criteria-
1. Men and women who are 20 years old or over and under 75 years of age
2. Those with BMI of 23 kg/m2 or more
3. Those with visceral fat area of 80 cm2 or more
1. Those who with hepatic, renal, heart disease, respiratory disorders, digestive disorders, endocrine disorders, metabolic disorders, neuropathy, consciousness disorders, diabetes, hyperlipidemia, hypertension, or other diseases and who are receiving medication treatment and are judged to be inappropriate by a doctor.
2. Those who take diabetes medications such as alpha-glucosidase inhibitors or biguanides that may affect the gut microbiota.
3. Pregnant women (those who plan to become pregnant)
4. Those who work night shifts at least once a week
5. Those who have a history of gastrointestinal resection (excluding appendectomy)
6. Those who have positive HBs antigen markers
7. Those who have positive HCV antibody markers
8. Those who have food allergies
9. Those who are allergic to metal (stainless steel) or have a pacemaker in their body
10. Those who have a history of malignant tumors
11. Those who have a history of mental illness
12. Those who have changes more than 2 kg of weight within 3 months of the start of this study
13. Those who regularly use pharmaceuticals, etc. that may affect the present study
14. Those who donated 200 mL or more of blood within one month of the start of the study, or those who plan to do so during the research period.
15. Those who cannot measure with a visceral fat measuring device
16. Other persons who are judged inappropriate by the principal investigator or the co-investigator
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method