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Clinical study on the efficacy of targeted scapular stabilization exercise on rotator cuff injury and prevention of shoulder pain recurrence

Clinical study on the efficacy of rehabilitation training based on scapular dyskinesia on rotator cuff injury and prevention of shoulder pain recurrence

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081262
Enrollment
Unknown
Registered
2024-02-27
Start date
2024-03-01
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Rotator cuff injury

Interventions

Scapular Stabilization Group:Rehabilitation based on the type of scapular dyskinesis
Traditional Exercise Group:Rehabilitation exercises such as pendulum, wall climbing and stick exercises

Sponsors

Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Be between 18 and 60 years of age; (2) Meet the diagnostic criteria for rotator cuff injury within the Clinical Diagnostic and Treatment Guide Orthopaedic Subsection; (3) Unilateral limb onset with or without limited joint mobility and shoulder pain with SD (type I-III); (4) A pain numerical rating scale (NRS) of =5 during shoulder motion; (5) Relevant imaging tests were available; (6) Patients volunteered to participate in the study and signed an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Those who have a total tear of the rotator cuff tendon and are temporarily not suitable for the rehabilitation training program in this study; (2) Shoulder fractures, dislocations, nerve injuries, cervical spondylosis, lung disease, heart disease, rheumatoid arthritis, and other disorders that cause shoulder pain; (3) Presence of scoliosis, kyphosis, history of spinal or lower extremity surgery, unequal length of both lower extremities, recent presence of acute fallout, or chronic cervical pain that would interfere with the results of the SD assessment; (4) Those whose body surface markers are not obvious enough to affect the assessment: Body Mass Index (BMI) >28, etc; (5) Shoulder flexion or abduction not exceeding 90 degrees; (6) Other conditions such as active infections, tumors, cognitive disorders, systemic diseases involving the joints, etc., which make it impossible to complete the designed exercise program; (7) Refusal to accept treatment.

Design outcomes

Primary

MeasureTime frame
Comprehensive Shoulder Function Score (Constant-Murley score, CMS);

Secondary

MeasureTime frame
Pain (Numerical rating scale, NRS);Scapular Stability Rating;Scapular dyskinesis evaluation;Satisfaction with shoulder function;Recurrence of shoulder pain;

Countries

China

Contacts

Public ContactChen Kang

Shanghai Sixth People's Hospital

njmuck@163.com+86 189 3017 4064

Outcome results

None listed

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