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The effect of the test substance on oral function, stress and immunity.

The effect of the test substance on oral function, stress and immunity. - The effect of the test substance on oral function, stress and immunity.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000042194
Enrollment
10
Registered
2020-10-22
Start date
2020-10-15
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

Taking bath once a day as more than 15 min submerged to the shoulder level in bathtub filled with hot water (below 41 degrees centigrade) which dissolved 4 tablets of test substance. Continue taking b

Sponsors

Chiyoda Oralhealth Care Clinic
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1) Female aged between 40 and 70 years old at when they were informed consent. 2) Must be able to bathe once a day during the test period. 3) A person who has received a full explanation of the purpose and content of the test and who understands the test and is able to obtain his or her written consent.

Exclusion criteria

Exclusion criteria: 1)Subjects who are treated by medicine continuously. 2)Subjects who regularly take functional food and/or health food which is expected to improve chilliness, blood-flow or body temperature, skin quality, stress, sleep and immunity. 3)Subjects who have previous and/or current medical history of serious disease in heart, liver, kidney, digestive organ, skin and central nervous system. 4)Subjects who have disease making unconsciousness at seizure, like arrhythmia, anemia, sleep apnea syndrome, epilepsy or diabetes.And subjects who are previous diagnosed as the same disease. 5)Pregnant or possibly pregnant women, or lactating women. 6)Subjects who have extremely irregular food habits. Subjects who have irregular life cycle because midnight-work or shift-work. 7)Subjects who are participating in the other clinical tests. Subjects who participated within 4 weeks prior to the current study and/or who plan to participate in the other clinical tests. 8)Subjects who have had skin symptoms such as itching and eczema, using bath additives in the past. 9)Subjects who have been judged as unsuitable for the study by the principal investigator or sub-investigator.

Design outcomes

Primary

MeasureTime frame
Confirmation of salivary quantity by Saxon test, Pittsburgh Sleep Quality Index, Secretory IgA.

Secondary

MeasureTime frame
Body temperature when wake up, Body temperature 1hr after bath, Body temperature before going to bed, With or without subjective symptom of chill, Blood flow, Skin moisture level, QOL Common Questionnaire.

Countries

Japan

Contacts

Public ContactMie Kaneko

Chiyoda Oralhealth Care Clinic None.

info@cocc.jp03-3288-8801

Outcome results

None listed

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