None listed
Conditions
Interventions
Using a higher humidity and lower temperature sauna at first visit. After rest period, using a higher temperature sauna at second visit.
Using a higher temperature sauna at first visit. After rest p
Sponsors
CPCC Company Limited
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: 1)Males aged 40 to 59 at registration. 2) Subjects who has systolic blood pressure less than 159 mmHg or diastolic blood pressure less than 99 mmHg in blood pressure measurement at pre-test 3) Subjects who are usually aware of a certain level of stress 4) Subjects giving written informed consent.
Exclusion criteria
Exclusion criteria: 1) Subjects who have been diagnosed with a mental disorder such as depression in the past, or are currently undergoing treatment. 2) Subjects who are continuing treatment with medicine. 3) Subjects who feels extremely frustrated and has trouble with everyday life. 4) Subjects who is aware that it is easy to dry in the mouth or little salivation. 5) Subjects who are claustrophobic and can not enter the sauna room. 6) Subjects who difficult to sweat in sauna bath. 7) Subjects who have tattoo. 8) Subjects who have wide barns scar. 9) Subjects with bruises, scratches, or acne on their cheeks. 10) Subjects who is severely sunburned or who works or plays sports outdoors for a long time. 11) Subjects who have special care on the face skin or arm skin (facial esthetics, body esthetics, facial care, peeling, laser treatment, hair removal etc.). 12) Subjects who plan to travel abroad or s wimming bath in the test period 13) Subjects who constantly use medicines, supplements having a possibility of affecting test results. 14) Subjects who have a history of and/or a history of serious illness in the heart, liver, kidney, digestive tract etc. 15) Subjects who excessive alcohol intake. 16) Subjects who have extremely irregular dining habits, and subjects who have midnight work or irregular shift work. 17) Subjects who are participating the other clinical tests. Subjects who participated within 4-weeks prior to the current study and/or who plan to participate the other clinical tests. 18) Others who have been determined ineligible by principal investigator or sub-investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Salivary cortisol, salivary IgA, salivary oxytocin | — |
Secondary
| Measure | Time frame |
|---|---|
| Salivary amylase, Salivary chromogranin, Skin moisture level, Blood pressure, Body temperature, Body weight, The incidence of side effects and/or adverse events | — |
Countries
Japan
Contacts
Public ContactMakoto Ichinohe
CPCC Company Limited Planning & Sales Department
Outcome results
None listed