Healthy volunteer
Conditions
Interventions
Visit-1 No intervention Visit-2 Exercise full set using ultra-soft rubber band size L(10 minutes) Visit-3 Exercise full set using ultra-soft rubber band size S(10 minutes) Visit-4 Exercise half set
Sponsors
Anti-Aging Bank Co.,Ltd.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: [1]Aged between 45 and 65 [2]Individuals who are healthy and do not treat any disease [3]Individuals whose written informed consent has been obtained [4]Individuals who can have an examination on a designated check day [5]Individuals judged appropriate for the study by the principal
Exclusion criteria
Exclusion criteria: [1]Individuals using medical products [2]Individuals under treatment or with history of lipid metabolism abnormality,hypertension, diabetes, mental disorders, sleep disorders, or other serious disorders [3]Individuals who used a drug to treat in the past 1 month (One-shot medicine of a headache, menstrual pain and a cold removes it.) [4]Individuals who have a history of serious hepatopathy, kidney damage, heart disease, lung disease,or blood disease [5]Individual who have digestive organ disease(disease of an appendix is removed) [6]Individuals with abnormal ECGs [7]Individuals whose BMI is less than 18.5 kg/m2 or over 30 kg/m2 [8]Individuals who donated blood over 200mL in the past 1 month or over 400mL in the past 3 months [9]Individuals with serious anemia [10]Individuals who have difficulty collecting blood over time [11]Individuals with daily exercise habits [12]Individuals who have difficulty exercising for 10 minutes [13]Individual who is based on average alcohol per 1 day and exceeds 60g/day [14]Individuals whose life style will change during the test period (ex. travel for a long time) [15]Individuals who had a habit to ingest health-promoting foods, foods for specified health uses, health foods, or supplyments of glycometabolism in the past 3 month or will ingest those foods during the test period [16]Individual who is pregnant or lactate [17]Individuals who participated in other clinical studies in the past three months [18]Individuals judged inappropriate for the study by the principal
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in blood glucose level and AUC / iAUC / Cmax / Tmax | — |
Countries
Japan
Contacts
Public ContactToshiyasu Tamura
TES Holdings Co., Ltd. Department of Clinical Trial
Outcome results
None listed