male/female adults
Conditions
Interventions
Sponsors
Suzuka University of Medical Science
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.Healty Subjects. 2.Subjects who are males or females and are aged 18 or older. 3.Subjects who have provided written consent for participation in the study.
Exclusion criteria
Exclusion criteria: 1.The persons who have taken Acanthopanax Senticosus and are not off it for more than 3 months. 2.Those who regularly use health foods that may affect the study. 3.Allergy to Acanthopanax Senticosus. 4.Subject who is not currently receiving treatment or medication. 5.Subject with current or history of alcohol dependence. 6.Those who are participating in other clinical studies. 7.Subject with severe diseases such as hepatic disorder, kidney disorder, heart disease. 8.Subject who have hepatitis. 9.Severe anemia. 10.Subjects with systolic blood pressure more than 180 mmHg or diastolic blood pressure more than 90 mmHg. 11.Other cases that the principal investigator and subinvestigators deem inappropriate as research subjects.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.Questionnaires for subjective 2.General Self-efficacy Scale (GSES) 3.OSA sleep inventory 4.STAI | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.salivary amylase 2.salivary cortisol 3.Autonomic activity 4.Objective sleep quality (measured using actigrapgh) | — |
Countries
Japan
Contacts
Public ContactFujishima Masaki
Sun Chlorella Corp. Production & Development Department Research & Development Group
Outcome results
None listed