None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Subject who voluntarily agrees to participate and sign in informed consent form 2) Healthy adults aged 30 to under 60 who complain of fatigue
Exclusion criteria
Exclusion criteria: 1) Subject who is unable to perform cycle ergometer test 2) Subject who constantly exercised for 3 months prior to the first visit 3) Those with a high level of cardiopulmonary endurance 4) Subject has a body mass index (BMI) of 18.5 kg / m2 or less or 30.0kg / m2 or more 5) Subject is over alcoholic : Men > 210g/week, Women > 140g/week 6) Smoker and drug addict 7) Insomnia 8) Subject have any of the following (including past medical history) or are taking any related medicines: hyperlipidemia, asthma, musculoskeletal disorder and etc 9) Subject who had a surgical operation 6 months prior to the first visit 10) Subjects who consumed oriental medicine within 1 month prior to the first visit 11) Subjects who consumed functional foods or related food to affect physical performance and fatigue 12) A person who continuously used a fatigue recovery injection within one month of his/her first visit. 13) Subject with hypersensitivity to the test food or ingredients contained in the test food 14) Pregnant or lactating women or person who has pregnancy plan during the study 15) Subject in other clinical trials within one month of the first visit or plan to participate in other clinical trials during this human study period 16) Subject unable to use smartphone or computer 17) Any condition that the principal investigator believes may put the subjects at undue risk
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| fatigue related indicators | — |
Secondary
| Measure | Time frame |
|---|---|
| Clinical pathology examination(Vital sings, clinical laboratory test) | — |
Countries
Korea, Republic of
Contacts
Seoul National University