A study about feeling of fatigue reduction effect of food containing algae
- Conditions
- Healthy adults
- Registration Number
- JPRN-UMIN000036296
- Lead Sponsor
- CPCC Company Limited
- Brief Summary
A significant reduction in feeling of physical fatigue was confirmed in the test food intake group.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 200
Not provided
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.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method