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Kinetic Chain Approach for Rotator Cuff Tendinopathy

Not Applicable
Recruiting
Conditions
Rotator Cuff Tendinopathy
Registration Number
NCT06838767
Lead Sponsor
Riphah International University
Brief Summary

The aim of this research is to determine the effectiveness of the kinetic chain approach on pain, functional disability and kinesiophobia in patient with rotator cuff tendinopathy. Randomized controlled trials done at National institute of rehabilitation and medicine. The sample size was 44. The subjects were divided in two groups, 22 subjects in Group A that received Conventional Treatment and 22 subjects in Group B that received Kinetic chain approach and conventional treatment. Study duration was of 6 months. Sampling technique applied was non probability connivance sampling technique. Patient with age between 40 to 65 years, Clinically diagnosed and Patients who meet the diagnostic criteria ≥ three positives in five shoulder impingement tests: Neer's sign, Hawkins and Kennedy test, Empty Can test, painful arc of abduction, and external rotation (ER) resistance test, Patients in acute (4 weeks) and sub-acute stage (4-6 weeks).Patients with positive scapular assistance test (SAT) and scapular retraction test (SRT). Were included. Tools used in the study are NPRS (Numeric Pain Rating Scale). SPADI (Shoulder Pain and Disability) .Tampa Scale for Kinesiophobia TSK-11. Data was be analyzed through SPSS -25

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
44
Inclusion Criteria
  • Both male and female.
  • Age between 40 to 65 years.
  • Clinically diagnosed and Patients who meet the diagnostic criteria ≥ three positives in five shoulder impingement tests: Neer's sign, Hawkins and Kennedy test, Empty Can test, painful arc of abduction, and external rotation (ER) resistance test (14)
  • Patients in acute (4 weeks) and sub-acute stage (4-6 weeks).
  • Patients with positive scapular assistance test (SAT) and scapular retraction test (SRT).
Exclusion Criteria
  • Patients with Cervical radiculopathy or previous shoulder surgery.

    • Any Participants with a full thickness tear of rotator cuff tendon.
    • History of glenohumeral dislocation, or other traumatic injury to the shoulder
    • Diagnosed patients of rheumatoid arthritis and osteoarthritis.
    • Hemiplegia affecting the shoulder and lower extremity
    • A complex myofascial pain syndrome.
    • History of significant lower extremity problems, including severe joint pain, recent fractures, or major musculoskeletal disorders (e.g. chronic ligament injuries)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
NPRS (Numeric Pain Rating Scale)6 weeks

NPRS (Numeric Pain Rating Scale) the NPRS is an 11-point ordinal system, used measure subject perceived level of pain .Assess pain intensity at baseline, 9 session and after 18 session

Secondary Outcome Measures
NameTimeMethod
SPADI (Shoulder Pain and Disability Index)6 weeks

SPADI (Shoulder Pain and Disability Index) is a patient completed questionnaire with 13 items. The pain subscale has 5-items and the Disability subscale has 8-items. Assess outcome at baseline , 9th session and after 18 session

Tampa Scale for Kinesiophobia TSK-116 weeks

Tampa Scale for Kinesiophobia TSK-11 Originally 17 item scale, used to identify fear or movement or re-injury. Assess outcome at baseline, after 9th session and after 18th session

Trial Locations

Locations (1)

National institute of rehabilitation medicine , polyclinic islamabad

🇵🇰

Islamabad, Punjab, Pakistan

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