None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Males aged 20 to 25 at registration. 2) Subjects giving written informed consent.
Exclusion criteria
Exclusion criteria: 1) Subjects who are regularly taking medicines or dietary supplements that may affect the results of the study. 2) Subjects with a history or current severe heart, liver, kidney or gastrointestinal disease. 3) Subjects who drink a lot of alcohol. 4) Subjects who smoke excessively. 5) Subjects with extremely irregular eating habits, irregular rhythm of life. 6) Subjects with allergies to medicines and foods (especially gelatin) 7) Subjects who are participating the other clinical tests. Subjects who participated within 4-weeks prior to the current study and/or who plan to participate the other clinical tests. 8) Subjects who have donated component blood or 200 mL of whole blood in the month prior to study entry. 9) Subjects who have donated 400 mL of whole blood in the 3 months prior to study entry. 10) Subjects who have donated 1200 mL of whole blood in the 12 months prior to study entry. 11) Subjects deemed by principal investigator to be ineligible to participate in this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual Analogue Scale to Evaluate Fatigue Severity (VAS-F), Survey on fatigue, Biological Antioxidant Potentia, Strength of one's back, Standing long jump, Shuttle run | — |
Secondary
| Measure | Time frame |
|---|---|
| Survey on tension and other issue, Skeletal muscle mass, Blood biochemistry test The incidence of side effects and/or adverse events | — |
Countries
Japan
Contacts
Shonan University of Medical Sciences Clinical Medicine Research Laboratory