obesity Sarcopenia
Conditions
Interventions
None listed
Sponsors
Kansai Medical University Health Science Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Selection Criteria Patients who meet all of the following criteria are eligible (1) Patients aged 20 years or older at the time of obtaining consent (2) Outpatient/inpatient: Any (3) Gender: No question (4) Patients who are able to use the physical activity meter used in this study (5) Patients who have received sufficient explanations for participation in this study and have given their free consent with full understanding.
Exclusion criteria
Exclusion criteria: Exclusion criteria Patients who violate any of the following will not be included in this study (1) Patients with severe hepatic or renal dysfunction (2) Pregnant or lactating women 3) Patients with a history of wasting disease or condition causing extreme weight loss (severe infection, invasive surgery, malignancy, severe trauma, hyperthyroidism, etc.) within the past 6 months (4) Patients after implantation of pacemakers and implantable defibrillators 5) Patients with psychiatric disorders that are difficult to manage (6) Patients who are unable to obtain written consent or who do not understand the outline and purpose of the research (7) Patients who are judged by the principal investigator to be inappropriate as research subjects.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoints of this study will be changes in skeletal muscle mass and body fat mass. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints will be body weight, blood pressure, glycolipid metabolic factors, adipokines, myokines, abdominal fat, arterial stiffness, physical fitness and physical activity, diet-related factors, and psychological indicators. | — |
Countries
Japan
Contacts
Public ContactSatoshi Kurose
Kansai Medical University Health Science Center
Outcome results
None listed