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Scapular Dyskinesis of Subacromial Impingement syndrome and development of appropriate rehabilitation techniques

Effects of selective kinesiotherapy for scapular dyskinesis in individuals with subacromial impingement syndrome

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17012521
Enrollment
Unknown
Registered
2017-08-31
Start date
2017-08-14
Completion date
Unknown
Last updated
2017-09-04

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

Conditions

subacromial impingement syndrome

Interventions

1:selective kinesiotherapy
2:nonselective kinesiotherapy

Sponsors

Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. unilateral shoulder pain for more than three months. 2. participants with SIS were enrolled in this trial according to clinical examination were positive for at least two of the following: (1) painful arc during flexion or abduction; (2) Neer test or Hawkins-Kennedy test, and (3) painful resisted external rotation, abduction or painful Jobe's test. 3. individuals who have signed the approval.

Exclusion criteria

Exclusion criteria: 1. bilateral shoulder pain; 2. professional overhead althetes or workers; 3. a scoliosis, kyphosis, severe cevical spondylosis or nerve injury; 4. participants who are intolerant to magnetic resonance imaging or surface electromyography; 5. previous traumatic shoulder fracture, complete rotator cuff tear, long head of biceps tendon injury, shoulder instability or severe shoulder arthritis; 6. inequality of lower extremity or long time with crutches; 7. BMI above 30Kg/m2.

Design outcomes

Primary

MeasureTime frame
Constant-Murley shoulder score;SPADI;

Secondary

MeasureTime frame
scapular dyskinesis evaluation;subacrmial distance;scapulothoracic muscle electromyographic activity;

Countries

China

Contacts

Public ContactYanhong Ma

Shanghai Sixth People's Hospital

myhmyh2006@126.com+86 18930177472

Outcome results

None listed

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