Investigation of the Effects of Kettlebell Training
1 other identifier
interventional
38
1 country
2
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Nov 2024
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 25, 2024
CompletedFirst Submitted
Initial submission to the registry
December 4, 2025
CompletedFirst Posted
Study publicly available on registry
December 17, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2026
CompletedDecember 17, 2025
December 1, 2025
1.1 years
December 4, 2025
December 4, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (6)
Shoulder Pain and Disability Index (SPADI)
It is a self-report questionnaire that measures pain and disability in the shoulder. It consists of 13 items in 2 subscales: pain (5 items) and disability (8 items). Items for both subscales are measured with visual analog scales ranging from 0 (no pain or difficulty) to 10 (worst pain imaginable or difficult enough to require assistance).
0th and 8th Week
Seated Single-Arm Shot-Put Test
Participants are placed in a position that does not restrict arm movement on the test side. In this position, they are instructed to hold a 3 kg ball in their hands at shoulder level with pain. Thus, from this initial positioning the participant pushes the ball as far as possible without noticing any compensation with the body. The evaluator administers the test independently and requests 3 applications at the participant's maximum capacity, with verbal stimulation and 1 minute rest between repetitions, and the average of these 3 applications is calculated.
0th and 8th Week
Upper Extremity Y Balance Test
For testing; The mechanism is established by combining 1.5 meter (m) lines in the medial, inferolateral and superolateral directions at appropriate angles. For the test, participants are asked to come into a push-up position and reach in all three directions with their free hands. Maximum reach distance will be recorded in centimeters (cm). In order to normalize the reach distances according to the limb length, the maximum values in each direction are summed, divided by 3 times the limb length and multiplied by 100.
0th and 8th Week
Closed Kinetic Chain Upper Extremity Stability Test
Individuals will be positioned in a push-up position with their bodies aligned in a straight line when viewed from the side, with a distance of 90 cm between their hands. Athletes will be asked to touch the dominant hand to the dorsum of the other hand within 15 seconds, and the total number of repetitions is recorded. The tests are repeated three times with a 45-second rest between tests and the average of the results is recorded.
0th and 8th Week
Evaluation of Shoulder Isometric Muscle Strength
Values resulting from isometric contraction will be recorded in kg. Muscle strength measurements will be evaluated bilaterally, in three repetitions, for 5 seconds. The average value of the triplicate results obtained will be recorded.
0th and 8th Week
Evaluation of Hand Grip Strength
Measurements were made while the individuals were standing, with the elbow and wrist in full extension. Measurements are repeated three times at 5-second intervals on the dominant and non-dominant hands (first right, then left and right again, etc.) and recorded in kilograms, and then their average is taken.
0th and 8th Week
Secondary Outcomes (1)
Global Rating of Change (GROC)
0th and 8th Week
Study Arms (2)
Exercise Group
EXPERIMENTALKettlebell Exercise Group
Control Group
ACTIVE COMPARATORStandard Rehabilitation Group
Interventions
8-week Kettlebell Exercises compare with 8-week Standard Rehabilitation Program
8-week Standard Rehabilitation Program compare with 8-week Kettlebell Exercises
Eligibility Criteria
You may qualify if:
- 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.)
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Hacettepe University
Ankara, Turkey (Türkiye)
Fenerbahce University
Istanbul, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Prof
Study Record Dates
First Submitted
December 4, 2025
First Posted
December 17, 2025
Study Start
November 25, 2024
Primary Completion
December 31, 2025
Study Completion
April 1, 2026
Last Updated
December 17, 2025
Record last verified: 2025-12
Data Sharing
- IPD Sharing
- Will not share