none (healthy adults)
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Those who give informed consent of participation before the study
Exclusion criteria
Exclusion criteria: Those who do not give informed consent of participation before the study Those who are decided to be unsuitable as a participant by the chief experimenter
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| amount of resting saliva (pre, post, and 10 minutes after the intervention) | — |
Secondary
| Measure | Time frame |
|---|---|
| subjective assessment of physical condition (after the intervention) | — |
Countries
Japan
Contacts
Institute of Biomedical Sciences, Tokushima University Graduate School Department of Oral Health Care and Rehabilitation