Healthy volunteers
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1)Males and Females whose age of 20 years or more and less than 65 years 2)Subjects receiving a sufficient briefing of the objective and content of the present study, fully understanding and agreeing to voluntary participate in the study and being able to personally sign a written informed consent
Exclusion criteria
Exclusion criteria: 1)Subjects receiving a medical treatment for serious renal, hepatic, cardio-vascular, respiratory, endocrine or metabolic disorders or having a medical history of these disorders 2)Subjects having the chronic fatigue syndrome (CFS), or subjects deemed to have severe fatigue like idiopathic chronic fatigue by the investigator 3)Subjects who take regularly pharmaceuticals or quasi-drugs which having the efficacy for recovery from fatigue or nutrient replenishment in case of physical fatigue 4)Subjects who take regularly Foods with Function Claims labeled the effect of attenuating fatigue sensation 5)Subjects who are currently taking part in another clinical study 6)Subjects who are pregnant or lactating, or intending to become pregnant during the study 7)Subjects deemed unsuitable by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Work performance evaluation [ATMT (ABC task), ATMT (Part B)] | — |
Secondary
| Measure | Time frame |
|---|---|
| VAS (fatigue sensation, sleepiness, motivation and concentration), Jikaku-sho shirabe, autonomic nervous function evaluation | — |
Countries
Japan
Contacts
Soiken Inc. R&D Division