Kinetic chain approach for treating rotator cuff tendinopathy
Effectiveness of Kinetic Chain Approach for Rotator Cuff Tendinopathy
NA · Riphah International University · NCT06838767
This study is testing if a new treatment method that focuses on the whole body can help people with rotator cuff tendinopathy feel less pain and move better when combined with standard care.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 44 (estimated) |
| Ages | 45 Years to 60 Years |
| Sex | All |
| Sponsor | Riphah International University (other) |
| Locations | 1 site (Islamabad, Punjab) |
| Trial ID | NCT06838767 on ClinicalTrials.gov |
What this trial studies
This research aims to evaluate the effectiveness of a kinetic chain approach combined with conventional treatment for patients suffering from rotator cuff tendinopathy. The study involves a randomized controlled trial with 44 participants, divided into two groups: one receiving conventional treatment and the other receiving the kinetic chain approach alongside conventional treatment. The trial will assess outcomes related to pain, functional disability, and kinesiophobia over a duration of six months. Participants must meet specific diagnostic criteria related to shoulder impingement tests.
Who should consider this trial
Good fit: Ideal candidates are males and females aged 40 to 65 years with clinically diagnosed rotator cuff tendinopathy in the acute or sub-acute stage.
Not a fit: Patients with cervical radiculopathy, previous shoulder surgery, or full thickness rotator cuff tears may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly reduce pain and improve functional outcomes for patients with rotator cuff tendinopathy.
How similar studies have performed: While the kinetic chain approach is a novel method in this context, similar studies have shown promise in improving outcomes for musculoskeletal conditions.
Eligibility criteria
Show full inclusion / exclusion criteria
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)
Where this trial is running
Islamabad, Punjab
- National institute of rehabilitation medicine , polyclinic islamabad — Islamabad, Punjab, Pakistan (RECRUITING)
Study contacts
- Principal investigator: Aneela Zia, MsOMPT — Riphah International University
- Study coordinator: Imran Amjad, phd
- Email: Imran.amjad@riphah.edu.pk
- Phone: 03324390125
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Rotator Cuff Tendinopathy, Rotator cuff injury, kinetic chain approach, pain, functional disability, kinesiophobia