A Study to Evaluate a Portable Body Composition Analyser (Fitrus Light)
- Conditions
- Not Applicable
- Registration Number
- KCT0009376
- Lead Sponsor
- Cheonan Korean Medicine Hospital of Daejeon University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 50
(1) Adults between the ages of 19 and 64 years old
(2) who have given voluntary written consent to participate in this clinical study
(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
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method