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Application and Multi-center Validation Clinical Study of an Intelligent Motion Assessment System Based on Computer Vision in Post-Joint Arthroscopy Rehabilitation of Multiple Joints

Application and Multi-center Validation Clinical Study of an Intelligent Motion Assessment System Based on Computer Vision in Post-Joint Arthroscopy Rehabilitation of Multiple Joints

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500113794
Enrollment
Unknown
Registered
2025-12-03
Start date
2025-12-30
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Postoperative assessment of shoulder, elbow, hip and knee arthroscopy

Interventions

Observation group:None

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Adults aged between 18 and 65 years old; 2. Patients who have undergone arthroscopic surgery, including knee arthroscopy, hip arthroscopy, shoulder arthroscopy or elbow arthroscopy, etc.; 3. Those without obvious neurological disorders or cognitive impairments before or after the surgery, and capable of independently completing the assessment actions; 4. Able to understand and cooperate with the assessment process and remote follow-up tasks; 5. Have given informed consent to participate in this study and have signed a written informed consent form.

Exclusion criteria

Exclusion criteria: 1. There are severe neurological disorders (such as stroke, Parkinson's disease, multiple sclerosis, etc.) that affect movement performance; 2. There are severe orthopedic diseases (such as major spinal deformities, severe multiple fractures) that impair normal movement ability; 3. There are serious postoperative complications such as severe infections, reoperations in the surgical area, or other major complications that may affect the recovery process; 4. There are severe psychological disorders or cognitive impairments that prevent the patient from completing standard assessment tasks; 5. During the postoperative assessment period, the patient plans to receive other interventional treatments (such as PRP injection, reoperation, etc.), which may affect the judgment of functional recovery independence; 6. Patients who are unwilling or unable to undergo multi-time point assessments or remote follow-ups.

Design outcomes

Primary

MeasureTime frame
Range of Motion;

Secondary

MeasureTime frame
Evaluation of lower limb load-bearing and stability;Three-dimensional gait analysis;Balance analysis;Patient Report outcomes, PROs;Psychological Function Questionnaire Assessment;

Countries

China

Contacts

Public ContactGang Chen

West China Hospital, Sichuan University

7422979@qq.com+86 189 8060 6707

Outcome results

None listed

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