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Clinical Trials in Turkey / NCT07289893
Recruiting Not applicable

Investigation of the Effects of Kettlebell Training

NCT07289893 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2024-11-25
Last updated
2025-12-17

Condition(s) studied

Shoulder PainRotator Cuff Injuries

Investigational drug(s) / intervention(s)

Kettlebell ExerciseStandard Exercise

Kettlebell Exercise: 8-week Kettlebell Exercises compare with 8-week Standard Rehabilitation Program

Standard Exercise: 8-week Standard Rehabilitation Program compare with 8-week Kettlebell Exercises

Study summary

Kettlebell exercises are seen as one of the approaches that can be used conservatively in individuals with shoulder pain. However, it is still unknown what results it has on its therapeutic effects. These findings highlight the need for higher quality studies evaluating the effects of kettlebell use and exercises for shoulder pain. Therefore, the purpose of this study was to investigate the effects of 8 weeks of kettlebell training on shoulder pain, function, and performance.

The hypotheses of our study are as follows:

* H1: In individuals with Rotator Cuff-Related Shoulder Pain, the improvement in shoulder-related pain perception is greater with Kettlebell training compared to the standard rehabilitation program.
* H2: In individuals with Rotator Cuff Related Shoulder Pain, shoulder function improvement is greater with Kettlebell training compared to the standard rehabilitation program.
* H3: In individuals with Rotator Cuff-Related Shoulder Pain, shoulder performance improvement is greater with Kettlebell training than with the standard rehabilitation program.

Eligibility

Sex
ALL
Min age
18 Years
Max age
35 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Individuals who are willing to participate and have been doing licensed/unlicensed amateur or professional sports for at least 3 years, * Individuals with Tegner Activity Scale ≥ 5, * A history of shoulder pain of at least 6 weeks, * At least 3 points measured using the 0 to 10 point Numerical Pain Scale (NPS), * Shoulder pain that worsens with resisted shoulder flexion, abduction or external rotation, * Rotator cuff tendinopathies, * Tears smaller than 1 cm, * Secondary shoulder instability without major trauma (due to rotator cuff muscle weakness, etc.) Exclusion Criteria: * History of fracture and/or surgery in the shoulder area, * Adhesive capsulitis, * Those with passive joint range of motion deficit, * Individuals with a positive Apprehension Test and/or Sulcus Sign test and multidirectional shoulder instability, * Numbness or tingling in the upper extremity with cervical compression test or upper extremity compression test, * Systemic or neurological disease, * Corticosteroid injection within 3 months before the intervention, * Physical therapy in the 6 months before the intervention, * Those with a history of dislocation and subluxation, * Those who are pregnant, * Those who did not participate in the study for 2 consecutive sessions

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Hacettepe University Ankara Turkey (Türkiye) Not Yet Recruiting
Fenerbahce University Istanbul Turkey (Türkiye) Recruiting

More Hacettepe 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 NCT07289893 on ClinicalTrials.gov ↗ ← All trials in Turkey