healthy individuals
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) Those who are 20 years of age or older at the time of obtaining consent (regardless of gender) 2) Those who have received sufficient explanation before participating in this study, and who have obtained the consent of the document by their own free will after sufficient understanding.
Exclusion criteria
Exclusion criteria: 1) Patients with severe hepatic or renal dysfunction 2) Uncontrolled diabetics 3) Women who are pregnant or may become pregnant 4) Lactating women 5) Patients who received other study drug or study drug within 3 months of obtaining consent 6) Those with arrhythmia 7) Persons whose main illness is mental illness 8) Those who lack the ability to express their intentions 9) In addition, those who the principal investigator deems inappropriate as research subjects
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rate of change in heart rate variability | — |
Secondary
| Measure | Time frame |
|---|---|
| psychological assessment external expression of QOL | — |
Countries
Japan
Contacts
Kansai Medical University Hospital Psychosomatic and General Internal Medicine