Healthy Adults
Conditions
Interventions
Participation in a 3-night 4-day fasting program Then, take 3 supplements for 31 days.
Take 3 supplements for 34 days.
Non-intervention
Sponsors
Akasaka Family Clinic
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Japanese who are 40 years old or under 64 years old 2) Persons who are healthy and do not have chronic physical or mental illnesses 3) Persons who received a sufficient explanation of the purpose and contents of the exam, have the capacity to consent, applied with free will with sufficient understanding, and agreed to participate with a written document 4) Persons with a BMI of 22 or higher 5) Persons who can come to the clinic on the designated day and undergo the examination 6) Persons who have been deemed suitable for participation in this study by the responsible physician.
Exclusion criteria
Exclusion criteria: 1) Persons who are currently suffering from some kind of disease and are judged by the investigator to need treatment 2) Persons with a history or current illness of severe disorders including liver, kidney, heart, lung, blood, digestive system, etc. 3) Persons with alcohol dependence or other mental disorders 4) Persons with a habit of taking medication for treatment of illness within the past month (excluding occasional use of medication for headache, menstrual pain, cold, etc.) 5) Persons who may develop seasonal allergy symptoms during the trial period, specific allergens include: Hanoki, Oobayashabushi, birch, sugi, hinoki, ragweed, mugwort, orchardgrass, and timothy grass 6) Persons who may experience allergic reactions to the ingredients in the test food, or those who may experience severe allergic reactions to other food or medication 7) Persons with severe anemia 8) Persons prone to contact dermatitis, those who have had it in the past, or those with sensitive fingertips 9) Persons who have a smoking habit 10) Women who are pregnant, nursing, planning to become pregnant during the trial period, or planning to become pregnant during the trial period 11) Persons who may change their lifestyle during the trial period (e.g., night shift work, long-term travel, etc.) 12) Persons who have habitually consumed functional food, health food, supplements containing ingredients of the test food within the past 3 months or plan to consume them during the trial period. 13) Persons who have received treatment requiring hospitalization within the past 6 months. 14) Persons who participate in other clinical studies or participated in the last 3 months or plan to participate in other clinical studies. 15) Persons who are judged by the investigator to be inappropriate for this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Total cholesterol, LDL, HDL, triglycerides, oxidized LDL, adiponectin, glucose, glycoalbumin, HbA1c,insulin, HOMA-IR Measure at before and after intervention. | — |
Secondary
| Measure | Time frame |
|---|---|
| Telomere length, G-tail length, protein, albumin, AST, ALT, Ca, Mg, Fe, Cu, ferritin, zinc, EPA, DHA, EPA/AA ratio, DHA/AA ratio, (EPA+DHA)/AA ratio, CRP, IL-6, TNFalpha, Hb, Ht, MCV, MHC, MCHC, systolic blood pressure, diastolic blood pressure, OSA-MA sleep quality test, POMS stress test, heavy metal mineral test, urinary 8-OHdG, height, weight, BMI, lean body mass Measure at before and after intervention. | — |
Countries
Japan
Contacts
Public ContactMitsuko Ito
Akasaka Family Clinic Clinic Director
Outcome results
None listed