- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05903300
Validation of the Polish Version of the MPIIQM Questionnaire for Musicians
July 24, 2023 updated by: Anna Cygańska
Validation of the Polish Version of the Musculoskeletal Pain Intensity and Interference Questionnaire for Musicians (MPIIQM-P)
The aim of this study, originally named "Cross-Cultural Adaptation and Validation of the Musculoskeletal Pain Intensity and Interference Questionnaire for Musicians of the Polish Population (MPIIQM-P)" is the enlargement of validation of the Polish questionnaire.
Study Overview
Status
Active, not recruiting
Conditions
Intervention / Treatment
Detailed Description
The aim is to determine the following psychometric properties: convergent and divergent validity, two-time reliability analysis, and exploratory factor analysis according to the recommended number of subjects of ≥45 subjects.
In addition, the aim of the study is to assess the psychometric properties of the MPIIQM-P questionnaire in the online version and to compare these results with the results for the paper version obtained by Cygańska et al., 2021.
Study Type
Observational
Enrollment (Actual)
182
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Warsaw, Poland
- Józef Piłsudski University of Physical Education in Warsaw
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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
Non-Probability Sample
Study Population
The study group consists of adult, professionally active people (women and men) who are professional orchestra musicians.
The mother tongue of the respondents must be Polish.
Description
Inclusion Criteria:
- permanent musician in an orchestra
- Polish as a native language
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 |
|---|---|
|
Professional orchestra musicians
The study group consists of adult, professionally active people (women and men) who are professional orchestra musicians.
The mother tongue of the respondents must be Polish.
|
The intervention consists of completing the MIPIM-P, QuickDash, and Brief Pain Inventory questionnaires.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain Intensity MPIQIM
Time Frame: Baseline and change between baseline and after few (3/4) days
|
The Musculoskeletal Pain Intensity and Interference Questionnaire for professional orchestra Musicians of the Polish Population (MPIIQM-P); The pain intensity score can be defined as the sum of the four pain intensity items (0-40, the higher the score, the greater the pain intensity) or the mean of pain intensity score (0-10, the higher the score, the greater the pain intensity).
|
Baseline and change between baseline and after few (3/4) days
|
|
Pain Intensity BPI
Time Frame: Baseline and change between baseline and after few (3/4) days
|
In Brief Pain Inventory, subjects rates their pain intensity on a numeric rating scale from 0 to 10, the higher the score, the greater the pain intensity.
The pain intensity score can be defined as the sum of the four pain intensity items (0-40, the higher the score, the greater the pain intensity).
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.
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Baseline and change between baseline and after few (3/4) days
|
|
Pain Interference MPIQIM
Time Frame: Baseline
|
The Musculoskeletal Pain Intensity and Interference Questionnaire for professional orchestra Musicians of the Polish Population (MPIIQM-P); The pain interference score can be defined as the sum of the four pain interference items (0-50, the higher the score, the greater the pain interference) or the mean of pain interference score (0-10, the higher the score, the greater the pain interference).
|
Baseline
|
|
Pain Interference BPI
Time Frame: Baseline
|
In Brief Pain Inventory, subjects rate their pain interference on a numeric rating scale from 0 to 10, the higher the score, the greater the pain interference.
The pain interference score can be defined as the sum of the four pain interference items (0-70, the higher the score, the greater the pain intensity) or the mean of the pain interference score (0-10, the higher the score, the greater the pain interference).
|
Baseline
|
|
Pain Interference
Time Frame: Baseline
|
In Quick Dash Questionaire, subjects rate their pain interference on a numeric rating scale from 0 to 5, the higher the score, the greater the pain interference.
The pain interference score can be defined as the sum of the selected answers, divided by 4 (i.e.
number of questions), subtracting 1, and multiply by 25.
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Anna K. Cygańska, Cygańska, Józef Piłsudski University of Physical Education in Warsaw
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 17, 2023
Primary Completion (Estimated)
October 28, 2023
Study Completion (Estimated)
December 1, 2023
Study Registration Dates
First Submitted
June 5, 2023
First Submitted That Met QC Criteria
June 5, 2023
First Posted (Actual)
June 15, 2023
Study Record Updates
Last Update Posted (Actual)
July 25, 2023
Last Update Submitted That Met QC Criteria
July 24, 2023
Last Verified
July 1, 2023
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- SKE 01-01/2023
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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