Preliminary study on reliability and validity of 3D motion sensor device for shoulder joint range of motion.

Not Applicable

• Conditions: Diseases of the musculoskeletal system and connective tissue

• Registration Number: KCT0008251
• Lead Sponsor: Kyung Hee University Oriental Medical Center

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 6 March 2023

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

[Healthy adult]
1. An adult aged 19 years or older who voluntarily decided to participate in this clinical study and signed a consent form

[Adhesive capsulitis]
1. Those with passive motion restrictions in two or more directions of the shoulder joint (flexion less than 165°, abduction less than 150°, external rotation less than 45°)
2. Those whose exercise restriction lasts for more than 1 month
3. An adult aged 19 years or older who voluntarily decided to participate in this clinical study and signed a consent form

Exclusion Criteria

[Healthy adult]
1. Those who have experienced a specific shoulder joint disease
2. Those who complain of shoulder pain
3. Patients who are expected to find it difficult to comply with the clinical study schedule
4. Patients who are difficult to participate in clinical research as judged by other researchers

[Adhesive capsulitis]
1. Those with other diseases such as rotator cuff tear on ultrasound or MRI
2. Patients who are expected to find it difficult to comply with the clinical study schedule
3. Patients who are difficult to participate in clinical research as judged by other researchers

Study & Design

• Study Type: Observational Study
• Study Design: Not specified