Healthy adults
Conditions
Interventions
Intake test food once a day at dinner time for 4 weeks.
Intake control food once a day at dinner time for 4 weeks.
Sponsors
CPCC Company Limited
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Healthy males and females aged 20 to 64 years old when consent acquisition. 2) Subjects who feel fatigue on daily basis. 3) Subjects who have received enough explanation about this study and were able to understand that, then giving written informed consent.
Exclusion criteria
Exclusion criteria: 1) Subjects who have previous and/or current medical history of serious disease (e.g., heart function, blood vessel, liver function, kidney function, pulmonary function, endocrine function, function of digestive organ and/or metabolism). 2) Subjects who have been diagnosed chronic fatigue syndrome, or subjects who are decided having severe fatigue such as idiopathic chronic fatigue by investigator and/or sub-investigator. 3) Subjects who are visiting hospital due to chronic disease. 4) Subjects who have psychiatric disease such as depression and/or schizophrenia. 5) Subjects who have impairment of sleep which need medical treatment. 6) Subjects who are likely to cause allergies against test food especially algae and/or seaweeds. 7) Subjects who constantly use oral medicines and/or quasi-drug having the effect of recovering from fatigue or the effect of supplementation when physical fatigue. 8) Subjects who constantly use food with functional claim about feeling of fatigue. 9) Subjects who excessive alcohol intake. 10) Subjects their BMI is less than 17 kg/m2 or equal and more than 30 kg/m2. 11) Subjects who are participating the other clinical tests. Subjects who participated within three month prior to the current study and/or who plan to participate the other clinical tests. 12) Subjects who donated over 200mL blood and/or blood components within the last one month to the current study. 13) Males who donated over 400mL blood and/or blood components within the last three month to the current study. 14) Females who donated over 400mL blood and/or blood components within the last four month to the current study. 15) Females who are pregnant or lactating, and females who could become pregnant or lactating during test period. 16) Others who have been determined ineligible by principal investigator or sub-investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| VAS questionnaire about feeling of fatigue (whole body feeling of fatigue, physical feeling of fatigue and psychological feeling of fatigue ) | — |
Secondary
| Measure | Time frame |
|---|---|
| *Profile of Mood States 2nd Edition *The incidence of side effects and/or adverse events | — |
Countries
Japan
Contacts
Public ContactMakoto Ichinohe
CPCC Company Limited Planning & Sales Department
Outcome results
None listed