Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
38 participants
INTERVENTIONAL
2024-11-25
2026-04-01
Brief Summary
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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.
Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
QUADRUPLE
Study Groups
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Exercise Group
Kettlebell Exercise Group
Kettlebell Exercise
8-week Kettlebell Exercises compare with 8-week Standard Rehabilitation Program
Control Group
Standard Rehabilitation Group
Standard Exercise
8-week Standard Rehabilitation Program compare with 8-week Kettlebell Exercises
Interventions
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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
Eligibility Criteria
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Inclusion Criteria
* 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
* 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
18 Years
35 Years
ALL
Yes
Sponsors
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Hacettepe University
OTHER
Responsible Party
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Elif Turgut
Prof
Locations
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Hacettepe University
Ankara, , Turkey (Türkiye)
Fenerbahce University
Istanbul, , Turkey (Türkiye)
Countries
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Facility Contacts
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Çağdaş Işıklar
Role: primary
Prof Sener
Role: primary
Other Identifiers
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30.01.2024
Identifier Type: -
Identifier Source: org_study_id