Prevalence of Musculoskeletal Disorders Among Musicians (nill)

May 13, 2026 updated by: The Jerzy Kukuczka Academy of Physical Education in Katowice

Assessment of the Prevalence of Playing-related Musculoskeletal Disorders Among Instrumental Musicians

Research conducted at the Faculty of Physiotherapy, Academy of Physical Education in Katowice, examines musculoskeletal disorders among instrumental musicians.

The study protocol was approved by the Ethics Committee of Polish Physiotherapy Associationon (Resolution No. 05/06/2025) on June 11, 2025.

The application form includes QuickDASH software enabling the functioning of the system and the MPIIQM-P system, which monitors the functioning of the musculoskeletal system and its impact on everyday musical performance.

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Recruiting

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.

Detailed Description

Participants are recruited via email and through Facebook groups and other social media platforms dedicated to musicians. If a participant agrees to participate in the study but is unable to complete the online survey, , a paper version will be made available.

Participants are asked to complete a voluntary survey consisting of three parts: 1/ metric data (age, gender, education, place of residence), 2/ questions about their instrument playing (type, instrument, duration and intensity of playing, etc.), and 3/ questions about musculoskeletal complaints using the QuickDASH (Upper Limb Disability Questionnaire) and the MPIIQM (Musculoskeletal Pain Intensity and Interference Questionnaire for Musicians).

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Observational

Enrollment (Estimated)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
450

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

The name and contact information for the person who can answer enrollment questions for a clinical study. Each location where the study is being conducted may also have a specific contact, who may be better able to answer those questions.

Study Contact Backup

Study Locations

  • Poland
      • Multiple Locations, Poland
        • Recruiting
        • Jerzy Kukuczka Academy of Physical Education in Katowice
        • Contact:

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

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

adults musician instrumentalists in Poland

Description

Inclusion Criteria:

  • consent to participate in the study,
  • over 18 years of age,
  • professionally active musician - instrumentalist or musician-hobbyist not working as a professionalist musician

Exclusion Criteria:

  • lack of consent to participate in the study, age under 18,
  • artist - singer,
  • pregnancy,
  • active cancer,
  • acute viral, bacterial or other infections,
  • current exacerbation of chronic diseases or other conditions that may affect playing the instrument (e.g. osteoarthritis, rheumatoid arthritis, ankylosing spondylitis, fibromyalgia, etc.),
  • previous surgeries and serious injuries of the musculoskeletal system (e.g. road accidents) within the last 5 years.

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

Group / Cohort

A group or subgroup of participants in an observational study that is assessed for biomedical or health outcomes.
Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.
1
professional musicians
Other: Survey using a questionnaire.
the QuickDASH questionnaire assessing the function of the upper limb and the MPIIQM-P questionnaire assessing the intensity of musculoskeletal pain and its impact on the musician's daily functioning
2
non-professional musicians
Other: Survey using a questionnaire.
the QuickDASH questionnaire assessing the function of the upper limb and the MPIIQM-P questionnaire assessing the intensity of musculoskeletal pain and its impact on the musician's daily functioning

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Measure Description
Time Frame
intensity of musculoskeletal pain and its impact on musican' daily functioning
Time Frame: through study completion, an average of 6 months
through study completion, an average of 6 months
Playing-related musculoskeletal disorders (PRMDs)
Time Frame: through study completion, an average of 6 motnths
Playing-related musculoskeletal disorders among musicians
through study completion, an average of 6 motnths

Collaborators and Investigators

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

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
The Jerzy Kukuczka Academy of Physical Education in Katowice

Investigators

Investigators

A researcher involved in a clinical study. Related terms include site principal investigator, site sub-investigator, study chair, study director, and study principal investigator.
  • Principal Investigator: Laura Piejko, PhD, The Jerzy Kukuczka Academy of Physical Education, Katowice, Poland

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

  • Prevalence and treatment of playing-related musculoskeletal disorders (PRMDs) related to head, neck and upper body region in musicians: A systematic review of randomized controlled trials. Physiotherapy Review, 2025, 29(4), 14-25 DOI: https://doi.org/10.5114/phr.2025.157936 Online publish date: 2025/12/22

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)

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
June 1, 2025

Primary Completion (Estimated)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
June 20, 2026

Study Completion (Estimated)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
June 30, 2026

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
April 8, 2026

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
May 13, 2026

First Posted (Actual)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
May 20, 2026

Study Record Updates

Last Update Posted (Actual)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
May 20, 2026

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
May 13, 2026

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
April 1, 2026

More Information

Terms related to this study

Keywords

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • Resolution no. 05/06/2025

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

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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