None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Patients with pain in any one of the knee, ankle, hip, lower back, wrist, neck, shoulder, or elbow. - Classify participants by pain severity based on the visual analogue scale (VAS) score. - Individuals aged 18 to 60 years. - Individuals with no abnormalities in joints other than the painful site. - Individuals who can decide for themselves and provide informed consent to participate in this study.
Exclusion criteria
Exclusion criteria: - Students supervised by the Principal Investigator (PI) and staff affiliated with the PI’s lab. - Hospitalized patients (inpatients). - Neurological abnormalities involving somatosensory function. - Perceptual or cognitive impairment. - Muscular dystrophy–related myopathy. - Skin disease or open wounds. - Fracture or osteoporosis. - Individuals exhibiting self-harm tendencies due to stress or other factors.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Comparison of joint-angle and muscle-activation data after long-term evaluation among the feedback-guided exercise group, the non-feedback exercise group, and the ultrasound stimulation group. | — |
Secondary
| Measure | Time frame |
|---|---|
| Accuracy assessment of the wearable band and the EMG sensor;Comparison of joint-angle and muscle-activation data during exercise between healthy individuals and patients with joint pain | — |
Countries
Korea, Republic of
Contacts
Korea Advanced Institute of Science and Technology