The Turkish Version of the Musculoskeletal Pain Intensity and Interference Questionnaire for Musicians (MPIIQM-T)

May 17, 2021 updated by: Ankara Yildirim Beyazıt University

The Turkish Version of the Musculoskeletal Pain Intensity and Interference Questionnaire for Musicians (MPIIQM-T): A Validity, Reliability and Cross-cultural Adaptation Study

The aim of this study, original named "The musculoskeletal pain intensity and interference questionnaire (MPIIQM)" is the Turkish validation, reliability and cross-cultural validation of the questionnaire.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Anticipated)

180

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 Locations

  • Turkey
      • Ankara, Turkey
        • Recruiting
        • Ankara Yildirim Beyazit University
        • 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

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

professional orchestra musician

Description

Inclusion Criteria:

  • permanent musician in an orchestra
  • understand and reading Turkish

Exclusion Criteria:

  • freelance musician

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
1
Other: The groups evaluated by The Musculoskeletal Pain Intensity and Interference Questionnaire for Professional Orchestra Musicians, Brief Pain Inventory, QuickDASH and Fatigue Severity Scale
The groups evaluated by The Musculoskeletal Pain Intensity and Interference Questionnaire for Professional Orchestra Musicians, Brief Pain Inventory, QuickDASH and Fatigue Severity Scale

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The Musculoskeletal Pain Intensity and Interference Questionnaire for Professional Orchestra Musicians
Time Frame: Baseline
The Musculoskeletal Pain Intensity and Interference Questionnaire for Professional Orchestra Musicians (MPIIQM) is a self-report questionnaire comprised of 22 items about performance-related musculoskeletal disorders (PRMD) in musicians. Age, gender and practice habits, different prevalence periods of PRMD, pain localization, pain intensity, pain interference are evaluated. The scoring of questionnaire is focused on the pain intensity and pain interference subscale. The pain intensity score can be defined as the sum of the four pain intensity items (0-40) or the mean of pain intensity score (0-10). The pain interference score can be defined as the sum of the five pain interference items (0-50) or the mean of pain interference score (0-10).
Baseline
The Musculoskeletal Pain Intensity and Interference Questionnaire for Professional Orchestra Musicians
Time Frame: 5 days after
The Musculoskeletal Pain Intensity and Interference Questionnaire for Professional Orchestra Musicians (MPIIQM) is a self-report questionnaire comprised of 22 items about performance-related musculoskeletal disorders (PRMD) in musicians. Age, gender and practice habits, different prevalence periods of PRMD, pain localization, pain intensity, pain interference are evaluated. The scoring of questionnaire is focused on the pain intensity and pain interference subscale. The pain intensity score can be defined as the sum of the four pain intensity items (0-40) or the mean of pain intensity score (0-10). The pain interference score can be defined as the sum of the five pain interference items (0-50) or the mean of pain interference score (0-10).
5 days after

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Brief Pain Inventory
Time Frame: Baseline
In Brief Pain Inventory, patients rate their pain severity and pain interference dimensions on a numeric rating scale from 0 to 10. In the inventory, a score of 1-4 is defined as mild pain, a score of 5-6 as moderate pain, and a score of 7-10 as severe pain.
Baseline
The QuickDASH
Time Frame: Baseline
The QuickDASH (Quick-Disabilities of the Arm, Shoulder and Hand Score) is a shortened version of the DASH (Disabilities of the Arm, Shoulder and Hand Score), featuring 11 instead of 30 items about physical function and symptoms in patients with musculoskeletal disorders of the upper extremities. 0-100 from each part of the Quick-DASH questionnaire (0 = no disability, 100 = most severe disability) is scored.
Baseline
The Fatigue Severity Scale
Time Frame: Baseline
The Fatigue Severity Scale (FSS) assess fatigue severity in a variety of medical conditions. It consists of 9 items rated on a 7-point Likert scale (1=strong disagreement, 7=strong agreement). High scores indicate fatigue. 28 points and above indicate the presence of severe fatigue.
Baseline

Collaborators and Investigators

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

Sponsor

Ankara Yildirim Beyazıt 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)

April 16, 2021

Primary Completion (Anticipated)

July 1, 2021

Study Completion (Anticipated)

July 1, 2021

Study Registration Dates

First Submitted

March 3, 2021

First Submitted That Met QC Criteria

March 3, 2021

First Posted (Actual)

March 5, 2021

Study Record Updates

Last Update Posted (Actual)

May 19, 2021

Last Update Submitted That Met QC Criteria

May 17, 2021

Last Verified

May 1, 2021

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 16.04.2021-44

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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