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Evaluation of the impact of the probiotic-containing dairy product on daytime work performance

Evaluation of the impact of the probiotic-containing dairy product on daytime work performance - Evaluation of the impact of the probiotic-containing dairy product on daytime work performance

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000055109
Enrollment
120
Registered
2025-07-30
Start date
2024-07-31
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Male/female adults

Interventions

Consumption of the test food (1 bottle a day) for 8 weeks Consumption of the placebo food (1 bottle a day) for 8 weeks

Sponsors

CPCC Company Limited
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Office workers 2. Subjects who are having sleep dissatisfaction 3. Subjects whose average sleep time on weekdays falls within the range of 4 to 7 hours 4. Right-handed subjects 5. Subjects who give written informed consent, after receiving a detailed explanation about the study and understanding the provided information.

Exclusion criteria

Exclusion criteria: 1. Subjects who have any clinically significant diseases, disorders or allergies to foods and drugs which in the investigator's opinion could interfere with the safety of study participants or with the results of the study. 2. Subjects who are currently receiving drug treatment. 3. Subjects who are trying to improve stress, sleep, and fatigue by taking functional foods or receiving therapies. 4. Subjects who are in living condition that can disturb their own sleep. 5. Subjects who have smoking habits. 6. Subjects who daily take excessive alcohol. 7. Subjects who work on irregular shifts or are engaged in physical labor. 8. Subjects who have exercise habits during nighttime and are unable to finish an exercise by 2 hours before bedtime. 9. Subjects whose sleeping environment is likely to change significantly during the study period due to a long trip or some others. 10. Subjects having wounds or other conditions on the area where the brain activity measuring device is to be attached 11. Subjects who have a participation in another interventional clinical study within the last 4 weeks or are intended to participate. 12. Females who are pregnant, intend to become pregnant, or breast-feeding. 13. Others who have been considered ineligible for the participation in the study by the investigators.

Design outcomes

Primary

MeasureTime frame
Perceived attention measured by subjective mood questionnaire (VAS)

Secondary

MeasureTime frame
Karolinska Sleepiness Scale for sleepiness Perceived fatigue, motivation, and optimism measured by subjective mood questionnaire (VAS) Cognitive task performance Brain activation during cognitive tasks

Countries

Japan

Contacts

Public ContactMasanori Numa

CPCC Company Limited Clinical Planning Department

cpcc-contact@cpcc.co.jp03-6225-9001

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026