A clinical study to evaluate to the effects of algae food on attenuating fatigue sensation.

Not Applicable

• Conditions: Healthy volunteers

• Registration Number: JPRN-UMIN000036314
• Lead Sponsor: Soiken Inc.

Brief Summary

The test food intake group showed significantly lower levels of physical and mental fatigue sensations than the placebo intake group.

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2019-06-22
• Study Start: 2020-03-29
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: All
• Target Recruitment: 66

Inclusion Criteria

Not provided

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 go to a doctor about chronic diseases 4) Subjects who have mental disease such as depression and schizophrenia 5) Subjects who have sleep disorders to need medical treatment 6) Subjects who have the possibility of developing allergic symptoms by the test food 7) Subjects who take regularly pharmaceuticals or quasi-drugs which having the efficacy for recovery from fatigue or nutrient replenishment in case of physical fatigue 8) Subjects who take regularly Foods with Function Claims labeled the effect of attenuating fatigue sensation 9) Subjects who drink a lot (Subjects whose pure alcohol intake per day is 60 g or more) 10) BMI<17 kg/m2 and >=30 kg/m2 11) Subjects having blood sample of 200 ml or more taken within 1 month, or 400 ml or more within 3 months prior to the start of the present study (e.g. donated blood) 12) Subjects who took part in another clinical study within 3 months prior to the start of the present study or who is currently taking part in another clinical study 13) Female subjects who are pregnant or lactating, or intending to become pregnant during the study 14) Subjects deemed unsuitable by the investigator

Study & Design

• Study Type: Interventional
• Study Design: Not specified