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Development of injury risk index based on kinematics analysis and EMG measurement and construction of a precise feedback-based rehabilitation system

Development of injury risk index based on kinematics analysis and EMG measurement and construction of a precise feedback rehabilitation system

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0011010
Enrollment
135
Registered
2025-09-10
Start date
2024-10-18
Completion date
Unknown
Last updated
2025-09-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Medical Device, Behavioral : ? Movement Task Experiment - Attach a wearable band, VICON markers, and EMG to each participant. - For the wearable band, attach sensors to the proximal and distal segment
attach EMG electrodes to the muscles responsible for that joint’s movement. (For the knee: wearable bands on the thigh and shank
EMG on the Rectus femoris, Biceps femoris, Tibialis anterior, and Gastrocnemius.) - Provide 5 minutes of practice for the exercise selected according to the target joint. - Perform 10 repetitions of t
patients with pain perform only the exercises for the affected joint. For the knee, the exercise is the single-leg squat.) ? Long-Term Exercise and Ultrasound Stimulation Experiment - Pre- and post-ex
EMG on the Rectus femoris, Biceps femoris, Tibialis anterior, and Gastrocnemius.) ? Perform 10 repetitions of the exercise selected for each joint and collect motion and muscle-activation data. (Healt
patients with pain perform only the exercises for the affected joint. For the knee, the exercise is the single-leg squat.) ? After the pre-test, randomly assign participants to the feedback exercise g

Sponsors

Korea Advanced Institute of Science and Technology
Lead Sponsor

Eligibility

Sex/Gender
All

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

MeasureTime 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

MeasureTime 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

Public ContactYoo-Jin Jun

Korea Advanced Institute of Science and Technology

ejjun727412@kaist.ac.kr+82-42-350-3078

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026