None listed
Conditions
Interventions
Dietary guidance for weight loss and visceral fat reduction will be provided once every two weeks for two months.
Sponsors
Macromill,Inc.
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: 1.Obese or lightly obese (Body Mass Index [BMI] >=25, If insufficient number of subjects, BMI >=23). 2.Person who has a diet intention. 3.Person who has a smartphone and can record meals and write a life diary using the app. 4.Person who agree to use the exercise and diet management app "Asken".
Exclusion criteria
Exclusion criteria: 1. Person who has suffer from chronic diseases currently (diabetes, hypertension, hyperlipidemia, gout, kidney disease, rheumatism, respiratory disease, etc.) and are taking medication. (however, users of drugs that suppress allergic symptoms such as allergic rhinitis can be included in the subjects) 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 who has deemed inappropriate to participate in this study by the principle investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Analysis of the relationship between weight loss / visceral fat loss before and after the intervention and other measurement items (physical test, blood test, etc.) | — |
Secondary
| Measure | Time frame |
|---|---|
| Comprehensive relevance analysis of all measurement items. | — |
Countries
Japan
Contacts
Public ContactMai Umeda
Kao Corporation Biological Science Research Lab.
Outcome results
None listed