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Rhythm-Based Stabilization Training in Video Gamers

NCT07387835 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 42

Last updated 2026-02-24

No results posted yet for this study

Summary

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.

Conditions

  • Scapular Dyskinesis

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

Sponsors & Collaborators

  • Istinye University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
35 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-02-15
Primary Completion
2026-04-25
Completion
2026-05-25

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07387835 on ClinicalTrials.gov