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Not yet recruiting NCT07387835

Rhythm-Based Stabilization Training in Video Gamers

No phase Interventional Scapular Dyskinesis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Rhythm-Based Scapular Stabilization Program, Posture education.
Who it may be relevant to
Registry conditions: Scapular Dyskinesis. Basic parameters: 18 years — 35 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

The Effect of Rhythm-Based Stabilization Training on Scapular Control, Upper Extremity Performance, and Range of Motion in Video Gamers.

Overview

This study aims to evaluate the effectiveness of a 4-week rhythm-based stabilization exercise protocol for professional video gamers diagnosed with scapular dyskinesis. Participants will undergo a structured exercise program consisting of 6 specific scapular stabilization exercises. These exercises will be performed on both stable surfaces (such as a treatment table or wall) and unstable surfaces (such as Swiss balls) to challenge neuromuscular control. The primary goal is to determine how this combined approach affects scapular control, upper extremity functional performance, and joint range of motion. Data will be collected through clinical assessments before and after the 4-week intervention to measure improvements in scapular stability and overall upper limb function.

Interventions

  • Other Rhythm-Based Scapular Stabilization Program
    "A 4-week exercise program consisting of 6 specific scapular stabilization exercises based on the rhythmic stabilization technique. The program includes 2 sets of 10 repetitions for each exercise, performed twice weekly. It utilizes both stable surfaces (wall/table) and unstable surfaces (Swiss balls) to challenge neuromuscular control and improve scapular stability in video gamers."
  • Other Posture education
    Posture education and general information

Primary outcome measures

  • Upper Quarter Closed Kinetic Chain Stability Test (UQCKCST) [Time frame: 4 weeks]
  • Reaction Time [Time frame: 4 weeks]
  • Lateral Scapular Shift Test [Time frame: 4 weeks]
  • Scapular Muscle Endurance Test [Time frame: 4 weeks]
  • Upper Quarter Y-Balance Test (YBT-UQ) [Time frame: 4 weeks]
  • Wrist Range of Motion (ROM) [Time frame: 4 weeks]
  • Medicine Ball Throw Test [Time frame: 4 weeks]
Secondary outcome measures (2)
  • Visual Analog Scale [Time frame: 4 weeks]
  • The Shoulder Pain and Disability Index [Time frame: 4 weeks]

Eligibility criteria

Inclusion criteria

  • Voluntary participants between 18 and 35 years of age
  • Playing video games for at least 3 hours per week for at least 3 months.
  • Healthy individuals with no chronic or acute shoulder/upper extremity problems.
  • Not participated in any other upper extremity treatment program in the last 6 months.
  • Willingness to participate and sign the informed consent form

Exclusion criteria

  • History of trauma, surgery, or fracture in the shoulder, neck, or hand in the last 6 months.
  • Diagnosis of any neurological disease (e.g., MS, Stroke).
  • Structural causes of upper extremity pain, such as disc herniation or radiculopathy.
  • Vestibular or balance disorders affecting upper extremity movement
  • Inability to perform required exercises due to severe pain or physical limitations

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Treatment

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07387835 · 2025-392

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗