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Exploratory study on the effects of lactic acid bacteria intake on mental and physical functions.

Exploratory study on the effects of lactic acid bacteria intake on mental and physical functions. - Exploratory study on the effects of lactic acid bacteria intake on mental and physical functions.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000051973
Enrollment
550
Registered
2023-10-17
Start date
2023-10-17
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

Healthy adults

Interventions

Take the test food once a day for 12 weeks

Sponsors

DeNA Life Science Inc.
Lead Sponsor
HOUSE WELLNESS FOODS CORPORATION
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)Healthy Japanese volunteers (male/female) aged 18 years or older at time of informed consent (2)Those who have already given written consent to participate in MYCODE study (the research aimed at improving health and longevity in Japan using data of the customers of MYCODE, a personal genome service). (3)Those who have received a sufficient explanation of the purpose of this study, have the ability to consent, are able to voluntarily apply for participation after having a good understanding of this study, and have given content for this study.

Exclusion criteria

Exclusion criteria: (1)Subjects who are receiving continuous pharmaceutical treatment (2)Subjects with previous and/or current medical history of serious disease (e.g. liver, kidney, heart, lung, blood) (3)Females who are pregnant and/or lactating, or those who may become pregnant (4)Subjects who plan to have irregular life cycle (e.g. midnight shift work, long-term travel) and/or those with extremely irregular dining and sleeping habits (5)Subjects who have a habit of taking foods containing Lactobacillus strains , which will be used in this study (6)Subjects who are participating in other clinical studies at the start of this study, or subjects who plan to participate in other clinical studies after providing consent for this study (7)Subjects who are judged unsuitable by the principal investigator

Design outcomes

Primary

MeasureTime frame
Self-reported questionnaires on the mental and physical health status.

Countries

Japan

Contacts

Public ContactTatsuya Matsuda

DeNA Life Science, Inc MYCODE service Dept

IRB_dls@dena.com03-4366-7219

Outcome results

None listed

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