🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Turkey / NCT05969652
Starting soon Not applicable

Comparison of the Effectiveness Heavy Slow Resistance and Eccentric Training in Rotator Cuff Tendinopathy

NCT05969652 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-01-31
Last updated
2024-06-27

Condition(s) studied

Rotator Cuff TendinopathySubacromial Impingement SyndromeBicep Tendinitis

Investigational drug(s) / intervention(s)

Heavy slow resistance trainingEccentric exercise training

Heavy slow resistance training: Patients will perform the exercises in the concentric and eccentric phases with the maximum amount of weight tolerated at a rate of 3 seconds/repetition. The number of sets\*repetitions is given below. 2-3 minutes rest between sets will be given. 1st week 3\*15 2-3.week 3\*12 4th-5th week 3\*10 6th week 3\*8

Eccentric exercise training: Among the patients in the eccentric exercise group, only the eccentric phase of the exercises in the HSR group, will be asked to actively engage with the affected party. The eccentric contraction rate will be set to 6 seconds. Each exercise will be done 3 sets of 15 repetitions. In the next week, progress will be made in exercise intensity according to tolerance and 500 g will be added to the previous weight. will be continued. If patients cannot tolerate the new weight or there is an increase in pain, the same weight will be continued for another week.

Study summary

Rotator cuff tendinopathy, also called subbracromial impingement syndrome, is one of the most important causes of anterior shoulder pain. Although exercise training is known as an effective intervention method in the treatment of rotator cuff/subacromial impingement problems, there is no definite consensus on which type of exercise is more effective. The aim of this study is to analyze and compare the effects of the Heavy Slow Resistance (HSR) training and eccentric exercise training on pain, function, supraspinatus tendon structure, muscle strength, range of motion, subjective perception of improvement and treatment satisfaction in individuals with subacromial shoulder pain associated with rotator cuff tendinopathy.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * Describing subacromial pain * Rotator cuff tendinopathy (subacromial impingement syndrome, biceps tendinitis and rotator cuff I. and II. stage diagnosis) * Continuation of diagnostic symptoms for at least 30 days Exclusion Criteria: * Prior shoulder surgery * Sign of cervical radiculopathy * Shoulder instability or history of upper extremity fracture * Full-thickness rotator cuff tear * Adhesive capsulitis * Humeroscapular periarthritis (osteoarthritis, inflammatory arthropathies, etc.) * Neoplasm/malignant status * Other independent from shoulder problem being on regular analgesic therapy for ongoing painful conditions * Subacromial corticosteroids in the last 2 months having received an injection or participating in a shoulder rehabilitation program

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Gazi University, Institute of Health Sciences, Department of Physiotherapy and Rehabilitation Ankara Çankaya

More Mustafa Kemal University trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05969652 on ClinicalTrials.gov ↗ ← All trials in Turkey