Male/female adults
Conditions
Interventions
Consumption of the test food (3 tablets a day) for 8 weeks
Consumption of the placebo food (3 tablets a day) for 8 weeks
Sponsors
CPCC Company Limited
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Men and women aged 25 to 49 years at the time of consent. 2. Subjects who have a habit of exercising for more than 5 hours per week. 3. Subjects who have perceived poor sleep quality for more than one month prior to consent acquisition. 4. Subjects who have perceived physical fatigue for more than one month prior to consent acquisition. 5. Subjects who can give informed consent to partake in this study, after being provided with an explanation of the protocol detail.
Exclusion criteria
Exclusion criteria: 1. Subjects currently undergoing medication or outpatient treatment for any serious disease, or those with a history of serious disease. 2. Subjects who cannot maintain their exercise habits and dietary habits from before the study during the trial period. 3. Subjects who are prone to diarrhea or have a weak stomach when consuming dairy products or foods containing lactic acid bacteria in excess. 4. Subjects with extremely irregular lifestyle habits, such as diet and sleep. 5. Subjects who are participating in the other clinical trials and/or who have participated in the other clinical trials within 4 weeks prior to the current trial and/or who are planning to participate in the other clinical trials. 6. Females who are pregnant or lactating, and females who could become pregnant during trial period. 7. Subjects with allergies to medications and/or food. 8. Subjects deemed unsuitable for participation in the trial by the study representative or the principal investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Subjective Mood Questionnaire | — |
Countries
Japan
Contacts
Public ContactMasanori Numa
CPCC Company Limited Clinical Planning Department
Outcome results
None listed