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Shoulder PainNCT07289893

Investigation of the Effects of Kettlebell Training

A study testing Kettlebell Exercise and Standard Exercise in people with Shoulder Pain and Rotator Cuff Injuries, run by Hacettepe University at 2 sites in Turkey (Türkiye).

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial 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. Read more about this study

Who is it for?
Ages 18 to 35 yearsHealthy volunteers can take part
Conditions the study is for
Shoulder Pain, Rotator Cuff Injuries
What is being tested?
Kettlebell Exercise and Standard Exercise
Could I receive a placebo?
No, everyone receives an active treatment
How many people
38 participants
Where
2 sitesTurkey (Türkiye)
Study dates
25 Nov 2024to 1 Apr 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 35 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • 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.)

Who cannot join

  • 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,
Show all 11Show fewer
  • 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

Trial locations and contacts

2 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Turkey (Türkiye)2 sites, 2 recruiting
  • Hacettepe University

    Ankara

    Çağdaş Işıklar, +905439638565, cagdasisiklar@gmail.com

    Elif Turgut

    Not yet recruiting
  • Fenerbahce University

    Istanbul

    Prof Sener, +902169101907, goksel.sener@fbu.edu.tr

    Recruiting

Other trials in Turkey (Türkiye)

About this study

Official title: Investigation of the Effects of Kettlebell Training on Pain, Function and Performance in Rotator Cuff-Related Shoulder Pain; Randomized Controlled Trial.

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.
Being tested
Kettlebell Exercise, Standard Exercise
Keywords
Kettlebell Exercises
Medical subject headings
Shoulder Pain, Rotator Cuff Injuries

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Kettlebell ExerciseOther

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

  • Standard ExerciseOther

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

Study groups in NCT07289893
Study groupRoleWhat they receive
Exercise GroupExperimentalKettlebell Exercise Group
Receives: Other: Kettlebell Exercise
Control GroupActive comparatorStandard Rehabilitation Group
Receives: Other: Standard Exercise

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. 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).

    Measured: 0th and 8th Week

  2. 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.

    Measured: 0th and 8th Week

  3. 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.

    Measured: 0th and 8th Week

  4. 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.

    Measured: 0th and 8th Week

  5. 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.

    Measured: 0th and 8th Week

  6. 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.

    Measured: 0th and 8th Week

Secondary outcomes (1)
  1. Global Rating of Change (GROC)

    This scale is a frequently used scale for the evaluation of clinical research in the musculoskeletal field. It is used to determine the improvement or deterioration of patients over a specified period of time. On the numerical scale, one represents "my pain has decreased a lot in a good way," while seven means "my pain has increased a lot in a bad way," and people report changes in pain compared to baseline.

    Measured: 0th and 8th Week

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted17 Dec 2025
  2. Study start25 Nov 2024
  3. Primary completion31 Dec 2025 (estimated)
  4. Study completion1 Apr 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
38 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07289893
Sponsor's protocol ID
30.01.2024
Status last verified
Dec 2025
First submitted
4 Dec 2025
Last updated
17 Dec 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Kettlebell Exercise and Standard Exercise in people with Shoulder Pain and Rotator Cuff Injuries, run by Hacettepe University at 2 sites in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 8 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: looking for participants now, as of the sponsor's last update on 17 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Each site lists its own contact: choose the nearest one under Trial locations. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Shoulder Pain and Disability Index (SPADI) (time frame: 0th and 8th Week). The study lists 6 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 17 Dec 2025; AzTrials last refreshed its copy on 7 Nov 2026.

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