Last reviewed · How we verify
NCT06838767
Kinetic Chain Approach for Rotator Cuff Tendinopathy
NA trial testing Conventional treatment in Rotator Cuff Tendinopathy in 44 participants. Completed in 29 August 2025.
28 August 2025
Quick facts
| Lead sponsor | Riphah International University |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 44 |
| Start date | 21 January 2024 |
| Primary completion | 28 August 2025 |
| Estimated completion | 29 August 2025 |
| Sites | 1 location across Pakistan |
Drugs / interventions tested
- Conventional treatment — full drug profile →
- Kinetic chain approach
Conditions studied
- Rotator Cuff Tendinopathy — all drugs for Rotator Cuff Tendinopathy →
Sponsor
Riphah International University
Who can join
Adults 45 to 60, any sex, with Rotator Cuff Tendinopathy. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
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
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT06838767
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Conventional treatment
Trials testing the same drug.
- NCT07514949 — The Feasibility and Safety of RK-4 Injection Bypassing Blood-brain Barrier in the Treatment of Acute Large Hemispheric I · NA · not yet recruiting
- NCT07518108 — The Role Of Fascia And Breathing Exercises In The Treatment Of Cervicogenic Headache · NA · not yet recruiting
- NCT07495150 — Intracalvariosseous Plus Intravenous Antibiotics for Moderate-to-Severe Bacterial Meningitis · NA · not yet recruiting
- NCT07462169 — High Intensity Laser VS High Power Pain Threshold Ultrasound in Treatment of Plantar Fasciitis · NA · not yet recruiting
- NCT07407088 — Effect of Virtual Reality-Supported Task-Oriented Training in Individuals With Rotator Cuff Lesions · NA · enrolling by invitation
Other recruiting trials for Rotator Cuff Tendinopathy
Currently open trials in the same condition.
- NCT06809543 — Clinical Benefits and Safety of Tropho Tend in the Management of Painful Rotator Cuff Tendinopathy · NA · recruiting
- NCT06517680 — Tight Control for Rotator Cuff Tendinopathy · NA · recruiting
- NCT07164625 — Telerehabilitation vs. In-person Physiotherapy in Young Elite Baseball Players · NA · active not recruiting
Other Riphah International University trials
Trials by the same sponsor.
- NCT07579585 — Effects of Photobiomodulation in Hemophilia Patients. · NA · recruiting
- NCT07504276 — Tele-Rehabilitation vs Conventional Rehabilitation for Cognitive Improvement in Stroke Survivors. · NA · recruiting
- NCT07484477 — Sedentary Behavior Modification, Cardiopulmonary Function & QOL Post Cardiac Surgery Patients. · NA · not yet recruiting
- NCT07438587 — Comparative Effects of Cadence Training vs Elliptical Training in Cricketers · NA · not yet recruiting
- NCT07484399 — Comparing Effects of HIIT and MICT on Functional Mobility, Muscle Strength, and Quality of Life in Diabetic Patients · NA · not yet recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06838767 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Riphah International University
- Last refreshed: 3 September 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06838767.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing