A study to evaluate the effect of food ingredient in healthy adult on the Fatigue reduction function -Placebo-controlled, randomized, double-blind, parallel-group comparative method
- Conditions
- Healthy adult
- Registration Number
- JPRN-UMIN000050852
- Lead Sponsor
- Hokkaido University of education
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 70
Not provided
(1) Those who have, are being treated for, or have a history of serious or metabolic diseases such as diabetes mellitus (2) Those who have chronic diseases and take drugs on a daily basis (3) Those who regularly use immunological or fatigue medications. (4) Those who are unable to stop consuming foods that contain a large amount of Bacillus acetate. (5) Those who cannot stop taking foods that contain a lot of lactobacilli and bifidobacteria. (6) Persons who deviate from proper alcohol consumption (7) Persons who reported to have food allergies (8) Those who are undergoing treatment that may affect the results of the study (9) Those who work day and night shifts or engage in physical labor such as heavy lifting. (10) Those who are engaged in physical labor such as working day and night shifts or heavy lifting. (11) Those who have a history of digestive organ disease or digestive organ surgery. (12)Pregnant women, women who intend to become pregnant during the study period, and breast-feeding women (13)Any person who is judged to be inappropriate as a research subject based on the results of screening tests (14)Persons with a history or current medical history of drug or alcohol dependence. (15) Those who are currently participating in a research study involving the ingestion of other foods or the use of pharmaceuticals, those who have participated in other clinical research studies within one month of obtaining consent, or those who intend to participate in such studies. (16)Those who plan to travel abroad, such as on an overseas trip, during the research period.Any other person whom the principal investigator determines to be inappropriate as a research subject.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method