None listed
Conditions
Interventions
Medical Device, Behavioral : We are using the electrical muslce stimulation device(BT-107).It wil be activated on rated pressure :3volt, rated power:50volt(used one of CR battery 2032),the quality of
t realize if they'
re disributed in real group or not.
The investigator will act the functional test in order to evaluate in 3 times. : before using EMS(Electricla Muscle Stimulation), after 4weeks, after 8weeks and com
Sponsors
Kyungpook National University Medical Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.adult (more than 20 years old) male and female 2.the subjects voluntarily agreed to this clinical trial and signed the agreement
Exclusion criteria
Exclusion criteria: 1.Those who have pacemaker( ex : cardiac pacemaker, phrenic nerve stimulator) 2.Severe systemic disease or chronic illness 3.Those who have not to apply the electrical pads owing to severe dermatitis 4.Those who have undergone other clinical / human application tests within 4 weeks prior to screening and have been treated with medical devices for clinical use. 5.A person who is judged to be ineligible to participate in this trial by other tester.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| first functional evaluation;secondary functional evaluation | — |
Secondary
| Measure | Time frame |
|---|---|
| Mcgill endurance test;Inbody test;manual abdominal circumference;visual inspection of abdominal muscle scale;abdominal CT;blood test;exercise torelance test;functional magnetic resonance imaging | — |
Countries
Korea, Republic of
Contacts
Public ContactMIN SUN
Kyungpook National University Medical Center
Outcome results
None listed