A confirmation test of fatigue feeling decreasing effect after exercise loading by test food consumptio

Not Applicable

• Conditions: Healthy adults

• Registration Number: JPRN-UMIN000038134
• Lead Sponsor: CPCC Company Limited

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2019-12-04
• Study Start: 2020-10-01
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

Not provided

Exclusion Criteria

Subjects who 1)are given continuous treatment by taking medicines. 2)ingest food for specified health use, functional foods, health foods and supplements (rich containing proteins, peptides and/or amino acids) more than 3 days a week. 3)use medicines that possibly have the influence for fatigue feeling more than 3 days a week. Subjects who ingest food for specified health use, functional foods, health foods and/or supplements those possibly have the influence for fatigue feeling more than 3 days a week. 4)are pregnant or lactating, and females who could become pregnant or lactating during test period. 5)have previous and/or current medical history of serious disease (e.g., heart, liver, kidney, digestive organ) containing history of surgical operations. 6)excessive alcohol intake. 7)smoke 8)have extremely irregular dining habits, and subjects who have midnight work or irregular shift work. 9)have previous medical history of drug and/or food allergy (especially to wheat and/or to soy bean). 10)are participating the other clinical tests. Subjects who participated within 4-weeks prior to the current study and/or who plan to participate the other clinical tests. 11)donated over 200mL blood and/or blood components within the last one month to the current study. 12)donated over 400mL blood and/or blood components within the last three month to the current study. And 13)Females who donated over 400mL blood and/or blood components within the last four month to the current study. 14)Males who will be collected over 1200mL blood and/or blood components, when the sampling amounts within the last twelve month are adding to the planned sampling amounts of this study. 15)Females who will be collected over 800mL blood and/or blood components when, the sampling amounts within the last twelve month are adding to the planned sampling amounts of this study. (16)Others who have been determined ineligible by principal investigator or sub-investigator.

Study & Design

• Study Type: Interventional
• Study Design: Not specified