None listed
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1) participants aged between 20 to 39 years 2) agreement on participation and providing written informed consent voluntarily after receiving a clear explanation of the clinical study purposes and characteristics. 3) participants without musculoskeletal disorders in the test joint area (shoulder joint)
Exclusion criteria
Exclusion criteria: 1) pregnant women and nursing mothers 2) history of liver, kidney, nervous system, immune system, respiratory, endocrine, cardiovascular, or circulatory disease, tumor, or mental illness 3) A person with a history of musculoskeletal disorders or mechanical abnormalities such as fractures, acute sprains, or tumors in the test site (shoulder joint) 4) Persons with severe disability in the shoulder movement due to severe pain at the joint site 5) Person who judged inappropriate for clinical examination by the examiner
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Shoulder joint`s Range of Motion (Flexion, Extension, Abduction) | — |
Secondary
| Measure | Time frame |
|---|---|
| The agreement between the motion analyzer and the measured value of POM Cheker | — |
Countries
Korea, Republic of
Contacts
Wonkwang University