None listed
Conditions
Interventions
Medical Device : If you are eligible for the study and meet the exclusion criteria, the test device (portable body composition analyzer (Fitrus Light)) and control device (Inbody570) will be administe
Sponsors
Cheonan Korean Medicine Hospital of Daejeon University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: (1) Adults between the ages of 19 and 64 years old (2) who have given voluntary written consent to participate in this clinical study
Exclusion criteria
Exclusion criteria: (1) Have taken dietary supplements or medications for weight control within 4 weeks of the first visit (2) Uncontrolled psychiatric illness, alcoholics (3) Participated in another clinical study within 1 month of the screening visit and received an intervention (4) Pregnant or breastfeeding women (5) Have had an implantable medical device, such as a pacemaker, etc. (6) Have had metallic materials inserted into the body (7) Those who have mobility problems and are unable to position themselves correctly for the examination. (8) Those with contagious diseases or wounds on the palms or soles of the feet (9) Those deemed inappropriate by the researcher to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Body fat (%) | — |
Secondary
| Measure | Time frame |
|---|---|
| Body fat (kg);Skeletal muscle mass (kg);Body water (L);Basal Metabolism (kcal) | — |
Countries
Korea, Republic of
Contacts
Public ContactJae-hui Kang
Cheonan Korean Medicine Hospital of Daejeon University
Outcome results
None listed