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Active, not recruitingNCT05903300Updated Jul 25, 2023

Validation of the Polish Version of the MPIIQM Questionnaire for Musicians

An observational study in Musculoskeletal Pain and Questionnaire, sponsored by Anna Cygańska. Active, not recruiting at 1 site in Poland. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2023-07-25.

Sponsored by Anna Cygańska · Observational

From the registry’s dates

  • Primary completion was expected by Oct 2023, 2 years 11 months ago, but the record still lists the study as active, not recruiting.
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
182
Ages
18 Years and older
Sex
All
01

Study summary

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.

Read the 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.

02

Conditions studied

  • Musculoskeletal Pain
  • Questionnaire

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Keywords

  • Occupational Diseases
  • Musculoskeletal Pain
  • Questionnaires
  • Validation Studies
  • Pain Measurement
03

In context

Musculoskeletal Pain

493 studies on the registry are indexed under Musculoskeletal Pain; 113 are open to participants now.

This study's enrollment of 182 is above the median of 163 across 136 observational studies indexed under Musculoskeletal Pain.

Browse Musculoskeletal Pain studies →

Lead sponsor

Anna Cygańska is the lead sponsor of 2 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
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.

Inclusion criteria

  • permanent musician in an orchestra
  • Polish as a native language

Exclusion criteria

Exclusion Criteria:

  • freelance musician
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
182 participants (actual)
Patient registry
No

Groups and cohorts

  • 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.

    Other: Surveys and Questionnaires

Interventions

  • OtherSurveys and Questionnaires

    The intervention consists of completing the MIPIM-P, QuickDash, and Brief Pain Inventory questionnaires.

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What researchers measure

Primary outcomes

  1. Pain Intensity MPIQIM

    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).

    Time frame: Baseline and change between baseline and after few (3/4) days

  2. Pain Intensity BPI

    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.

    Time frame: Baseline and change between baseline and after few (3/4) days

  3. Pain Interference MPIQIM

    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).

    Time frame: Baseline

  4. Pain Interference BPI

    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).

    Time frame: Baseline

  5. Pain Interference

    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.

    Time frame: Baseline

07

Study locations

1 site
  • Józef Piłsudski University of Physical Education in Warsaw
    Warsaw, Poland
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 25, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05903300
Lead sponsor
Anna Cygańska
Responsible party
Anna Cygańska (Principal Investigator, PhD in physical culture science, Józef Piłsudski University of Physical Education) — Sponsor-investigator
First posted
Jun 15, 2023
Start date
Apr 17, 2023
Primary completion
Oct 28, 2023 (estimated)
Completion
Dec 1, 2023 (estimated)
Last update
Jul 25, 2023

Study contacts

Anna K. Cygańska, Cygańska
principal investigator · Józef Piłsudski University of Physical Education in Warsaw

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Jul 2023. You cannot join it, but the record below documents what was studied.

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