1. metabolic syndrome 2. obesity,
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Independent person 20 years or older at time of consent 2.Is receiving lifestyle disease counseling at health sciences center 3.Understands the tools, tests and other elements of this study, and is capable of using and implementing them 4.Has received a full explanation of participation in this study and given their written consent of their own accord
Exclusion criteria
Exclusion criteria: 1.Person for whom spontaneous physical activity is difficult 2.Is being treated with antidepressants and antipsychotics, and has cranial neuropathy 3.Is receiving unstable treatment for diabetes, hypertension, etc. 4.Has otherwise been deemed unsuitable as a research subject by an investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Collect continuous activity records for bodily movements and sleep (amount of exercise, exercise time, sustained exercise time, exercise intensity, exercise patterns, diurnal cycles, weekly cycles, exercise normality, non-normality (=irregularity), sleep time, sleep start time, sleep latency, sleep depth), and then study the connection between to the physical and psychological secondary endpoints below, as well as the amount of change after six-month intervention. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Body composition (inBody720) 2.Arteriosclerosis risk factors 3.Saliva amylase 4.Blood (peripheral blood figure, blood glucose, HbA1c, lipids, hepatic function, renal function) 5.BDI-II(Beck depression questionnaire-II) 6.PHQ9 (Patient Health Questionnaire-9) 7.CES-D (depression self-assessment scale) 8.TEG-II(Tokyo University Egogram New Ver. II) 9.NEO-FFI (NEO-FFI personality test) 10.POMS2 (Profile of Mood States 2nd Edition) | — |
Countries
Japan
Contacts
1)Osaka Sangyo University, 2)Kansai Medical University 1)Faculty of International Studies, 2)Health Science