None listed
Conditions
Interventions
None listed
Sponsors
Kyung Hee University Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Patients who have undergone rotator cuff repair surgery after the date of IRB approval 2) Male and female patients aged 18 to 64 years 3) Individuals who are able to comply with postoperative visits and evaluations
Exclusion criteria
Exclusion criteria: 1) Patients with a history of surgery on the ipsilateral shoulder 2) Patients with infection or rheumatoid arthritis in the ipsilateral shoulder 3) Patients with cervical spine disorders causing shoulder pain 4) Patients with bilateral shoulder pain or limited range of motion in both shoulders 5) Patients with shoulder pain caused by trauma 6) Patients who are unable to attend follow-up visits for more than 3 months 7) Patients who do not consent to participate in the study 8) Patients currently participating in another clinical trial 9) Patients who have received rehabilitation at a hospital other than the study site 10) Patients with psychiatric disorders, risk of dementia, or otherwise deemed unsuitable for the study by the principal investigator 11) Pregnant women or illiterate individuals
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Range of motion measured with goniometer | — |
Secondary
| Measure | Time frame |
|---|---|
| Pain visual analogue scale (VAS);American Shoulder and Elbow Surgeons score;Range of motion measured with goniometer;Exercise completion rate;Technology acceptance / resistance to innovation questionnaire | — |
Countries
Korea, Republic of
Contacts
Public ContactSung Min Rhee
Kyung Hee University Hospital
Outcome results
None listed