Degenerative Disease, Healthy
Conditions
Brief summary
To develop biomechanical indicators for pain-inducing lifestyles and apply lifestyle strategies for patients and confirm their effectiveness to be used in artificial intelligence-based digital treatment devices.
Detailed description
To develop biomechanical indicators for pain-inducing lifestyles and apply lifestyle strategies for patients and confirm their effectiveness to be used in artificial intelligence-based digital treatment devices for patients who complain degenerative knee and back pain.
Interventions
None listed
Sponsors
Bundang CHA Hospital
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
1. Normal subjects * Inclusion criteria 1. Over 19 years of age 2. Those who scored '0' on the Knee/Back Pain Assessment Scale (VAS) 3. After hearing a detailed explanation of this study and fully understanding it, the subject or legal representative voluntarily decides to participate and agrees in writing to observe the precautions *
Exclusion criteria
1. Patients who correspond to one or more of the following cannot participate in the study. 2. Those with systemic infectious symptoms at the time of participation in the study 3. Persons with poor systemic conditions such as unstable conditions of the cardiovascular system, digestive system, respiratory system, endocrine system, etc., and those with cerebrovascular disease 4. Other cases where the researcher judges that participation in this study is not suitable (Patients who are participating in other studies or who have participated in other studies within the past 30 days can also participate in this study.) 2. Subjects who complain pain by degenrative changes in knee * Inclusion criteria 1. Over 19 years of age 2. Those who scored '1' or higher on the Knee Pain Assessment Scale (VAS) 3. After hearing a detailed explanation of this study and fully understanding it, the subject or legal representative voluntarily decides to participate and agrees in writing to observe the precautions *
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Motion analysis | 1 day after screening assessment | Motion capture analysis for kinetic and kinematic data |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Ground reaction force | 1 day after screening assessment | GRF measurement for ground reaction force in newtone |
| EMG measurement | 1 day after screening assessment | Electromyography in maximum voluntary contraction |
Countries
South Korea
Contacts
Primary ContactHyun Jung Oh, Bachelor
Outcome results
None listed