Kinematics and Muscle Activation of Scapula in Upper String Players With Neck Pain

May 11, 2026 updated by: Yin-Liang Lin, National Yang Ming Chiao Tung University
This study will analyze and compare scapular kinematics and muscle activation patterns between upper string musicians with and without neck pain during arm elevation and playing tasks (open strings, scales, musical pieces), providing insights for performance training and rehabilitation programs to reduce playing-related musculoskeletal disorders.

Study Overview

Detailed Description

The study participants will be right-handed upper string musicians (violinists and violists) aged 18 years and older. Participants must have at least 5 years of playing experience and practice more than 6 hours per week.

Neck pain group: non-specific neck pain (between superior nuchal line and T1) lasting at least 2 weeks with NRS ≥3.

Healthy control group: no neck/shoulder pain history in the past year, matched for age, gender, handedness, playing experience (>5 years), and practice hours (>6 hours/week).

The study involves arm elevation (0°, 30°, 60°, 90°, 120°); open string playing (at 60-120 bpm); A major scale (at 60-120 bpm); E major scale (at 60-120 bpm); and Vittorio Monti Csárdás.

Study Type

Observational

Enrollment (Estimated)

60

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • Taiwan
      • Taipei, Taiwan, Taiwan, 112
        • Recruiting
        • National Yang Ming Chiao Tung University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

upper string musicians

Description

Inclusion Criteria:

  • Age ≥ 18 years old.
  • Having at least 5 years of string instrument playing experience and practicing for more than 6 hours per week.
  • For the neck pain group: Experiencing non-specific neck pain for at least 2 weeks, with pain located between the superior nuchal line and the T1 spinous process, and a pain intensity of at least 3 on the Numeric Rating Scale (NRS ≥ 3).
  • For the healthy control group: Having no history of neck or shoulder pain within the past year (matched with the neck pain group by age, gender, and handedness).

Exclusion Criteria:

  • History of any neck or shoulder surgery or fracture.
  • Experiencing pain below the elbow with an intensity of at least 3 (NRS ≥ 3).
  • Diagnosed history of any structural cervical spine issues, such as herniation of intervertebral disc (HIVD), cervical spine spondylosis, or spondylolisthesis.
  • Positive response on any of the following 5 cervical spine screening tests: cervical distraction test, Spurling's test, Valsalva test, rotational alar ligament stress test, or Sharp-Purser test.
  • Any neurological disorders.
  • Pregnancy during the study period.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
upper string musicians (healthy group)
upper string musicians without non-specific neck pain
Arm elevation (0°, 30°, 60°, 90°, 120°), open string playing, scale practice, and musical piece performance
upper string musicians (neck pain group)
upper string musicians with non-specific neck pain
Arm elevation (0°, 30°, 60°, 90°, 120°), open string playing, scale practice, and musical piece performance

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Scapular muscles activation during arm elevation and dynamic instrument-playing tasks.
Time Frame: Through study completion, an average of 1 hour
Muscle activation levels of the upper trapezius, lower trapezius, and serratus anterior will be measured using surface electromyography (sEMG) during arm elevation (0°, 30°, 60°, 90°, 120°) and dynamic instrument-playing tasks. Data will be normalized to maximum voluntary isometric contraction (%MVIC) and expressed as root mean square (RMS) amplitude.
Through study completion, an average of 1 hour
Scapular kinematics during arm elevation and dynamic instrument-playing tasks
Time Frame: Through study completion, an average of 1 hour
Three-dimensional scapular orientation (upward/downward rotation, internal/external rotation, anterior/posterior tilt) will be measured using an electromagnetic tracking system during arm elevation (0°, 30°, 60°, 90°, 120°) and dynamic instrument-playing tasks. Data will be expressed in degrees.
Through study completion, an average of 1 hour

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Cervical muscles activation during arm elevation and dynamic instrument-playing tasks
Time Frame: : Through study completion, an average of 1 hour
Muscle activation levels of the sternocleidomastoid (SCM) and cervical extensors (CE) will be measured using surface electromyography (sEMG) during arm elevation and dynamic instrument-playing tasks. Data will be normalized to maximum voluntary isometric contraction (%MVIC) and expressed as root mean square (RMS) amplitude.
: Through study completion, an average of 1 hour
Cervical kinematic during arm elevation and dynamic instrument-playing tasks
Time Frame: Through study completion, an average of 1 hour
Three-dimensional movement of the cervical spine will be measured using the VIPER electromagnetic tracking system during arm elevation and dynamic instrument-playing tasks. Data will be expressed in degrees.
Through study completion, an average of 1 hour
Shoulder muscle strength
Time Frame: Immediately during the experiment
Isometric muscle strength of the upper/lower trapezius, and serratus anterior muscles will be evaluated using a hand-held dynamometer (MicroFET2). Data will be expressed in kilograms (kg).
Immediately during the experiment
Cervical and Shoulder mobility
Time Frame: Immediately during the experiment
cervical range of motion (flexion, extension, lateral flexion, rotation) will be measured using CROM. Shoulder range of motion will be measured using inclinometer. Data will be expressed in degrees (°).
Immediately during the experiment
Shoulder muscle length test
Time Frame: Immediately during the experiment
Resting length of the pectoralis minor and levator scapulae muscles will be measured using a tape measure and vernier caliper. Pectoralis minor index (PMI) and levator scapulae index (LSI) will be calculated and expressed as percentages (%). Pectoralis major flexibility assessed in supine via ability to rest the posterior shoulder flat on the table (pass/fail).
Immediately during the experiment
Postural Angles (CVA and FSA)
Time Frame: Immediately during the experiment
Craniovertebral angle (CVA) and forward shoulder angle (FSA) will be measured using digital photography to assess static head and shoulder posture.
Immediately during the experiment

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: YIN-LIANG LIN, PhD, National Yang Ming Chiao Tung University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 10, 2026

Primary Completion (Estimated)

September 30, 2026

Study Completion (Estimated)

December 31, 2026

Study Registration Dates

First Submitted

February 26, 2026

First Submitted That Met QC Criteria

February 26, 2026

First Posted (Actual)

March 4, 2026

Study Record Updates

Last Update Posted (Actual)

May 14, 2026

Last Update Submitted That Met QC Criteria

May 11, 2026

Last Verified

May 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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