Exercise Intervention Obesity Improvement Trial 2023
- Conditions
- ot applicable
- Registration Number
- JPRN-UMIN000051802
- Lead Sponsor
- Macromill,Inc.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Male
- Target Recruitment
- 60
Not provided
1. Person who has suffer from chronic diseases currently (diabetes, hypertension, hyperlipidemia, gout, kidney disease, rheumatism, respiratory disease, etc.) and are taking medication. 2. Person who has difficulty participating in research due to liver, kidney, heart disease, respiratory disorder, endocrine disorder, metabolic disorder, neurological disorder, consciousness disorder, diabetes, or other diseases. 3. Person who with alcoholic drinkers. (alcohol equivalent 60g / day or more) : (Beer: 3 medium bottles (1.5L), Sake: 3 go (540ml), Whiskey: 3 double glasses (180ml), Shochu: 1.8go (330ml) or more) 4. Person who has a history of gastrointestinal resection (excluding cecal resection). 5. Person who has collected 200 mL of blood (donated blood, etc.) within 1 month or 400 mL or more within 3 months of the start of this study. 6. Person who has skin diseases (atopic dermatitis, acne vulgaris, psoriasis, etc.) on face. 7. Person who use medical external medicine on the face. 8. Person who has excessive sunburn on the face. 9. Person who has skin diseases, metal allergies, pacemakers, etc. in their bodies. 10. Person who plan to participate in other clinical trials during the trial participation period. 11. Person who are not day shifts such as night shifts and rotation shifts. 12. Person who has felt sick at the time of blood collection, or person who has difficulty in collecting blood because the blood vessels in the arm are difficult to see. 13. Person who has a history of drug dependence, alcohol dependence, or current medical history. 14. Person who has plan to travel or travel for more than 2 weeks during the test period. 15. Person with low physical fitness who cannot exercise (such as walking fast for 20 minutes or more), or person who have orthopedic area disease or orthopedic chronic disease. 16. Person who has deemed inappropriate to participate in this study by the principle investigator.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method