Effect of preoperative rehabilitation on clinical outcomes after rotator cuff repair

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0007572

Enrollment

Registered

2022-07-27

Start date

2022-08-03

Completion date

Unknown

Last updated

2022-09-20

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

Conditions

None listed

Interventions

Behavioral : Subjects are randomly assigned to one of two rehabilitation training periods(preoperative rehabilitation or postoperative rehabilitation). For random placement, the 40 cards labeled grou

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) Among the patients who visited our orthopedic outpatient clinic for unilateral shoulder pain, according to the classification of DeOrio and Cofield, a rotator cuff tear was diagnosed as a medium tear (1-3 cm) or less, and among patients scheduled for surgery, those who agreed to this study 2) Patients with 3 weeks or more left until surgery

Exclusion criteria

Exclusion criteria: 1) Patients with frozen shoulder, shoulder arthritis, or other shoulder joint disease such as shoulder instability 2) Patients with a history of shoulder joint surgery 3) Patients with bleeding tendency 4) Patients with inflammatory musculoskeletal system such as rheumatoid arthritis and spondyloarthropathies

Design outcomes

Primary

Measure	Time frame
visual analogue scale(VAS), University of California Los Angeles scale (UCLA), American Shoulder and Elbow Surgeon's scale (ASES), Subjective shoulder value (SSV), SF-36v2	—

Secondary

Measure	Time frame
range of motion(ROM), x-ray;Magnetic Resonance Imaging (MRI);sonogram(sono)	—

Countries

Korea, Republic of

Contacts

Public ContactDu-Han Kim

Keimyung University

osmdkdh@gmail.com+82-53-258-7930

Outcome results