"Validation and Reability of the Munich Shoulder Questionnaire Into Turkish Patients" (MSQ)

May 17, 2019 updated by: Deniz KOCAMAZ, Hasan Kalyoncu University

Cultural Adaptation, Validation and Reability of the Munich Shoulder Questionnaire Into Turkish Patients With Shoulder Dysfunction

The purpose of this study was to translate and culturally adapt the MSQ to Turkish language and test the validity and reliability of Turkish version of MSQ in shoulder dysfunction patients. And also, the ultimate goal was to facilitate international researches in shoulder problems as well as to serve the physicians for their clinical practice.

Study Overview

Detailed Description

Munich Shoulder Questionnaire (MSQ) is an innovative tool for self-assessment of shoulder function. It was especially designed for an effective follow-up of shoulder patients which were also allowing for a quantitative assessment of the Constant, Shoulder Pain and Disability Index (SPADI) and DASH score consisting of a 30-items questionnaire. It based on subjective and objective parameters of shoulder function.

Standart questionnaire enable to follow patients on a close and regular base with manageable effort for both the disability and the patients.an optimal instrument for outcome measurement of shoulder problems should meet the following requirments: a) the instrument should be a self-assmment patient reporting tool, b) the questions must be easily comprensible, c) filling in should be finished less than 30 minutes, d) the results should provide calculation of several well established scoring system. MSQ can be completed at home and typical functional abilities about evaluation are explained with pictures so these can make it easy. As a result, we choose to translate the MSQ into Turkish as it is less costly, practical and time consuming than developing a new tool. In addition, objective (normal joint movement and muscle strength) and subjective (pain, daily life activity, sport and leisure time activities) parameters in a single form to create the advantage in terms of ease of use and time. With these properties, MSQ may be preferred during follow-up of the results of conservative and / or surgical treatment.

Study Type

Observational

Enrollment (Actual)

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 Locations

      • Gaziantep, Turkey, 27410
        • Deni̇z Kocamaz

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

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

shoulder dysfunction

Description

Inclusion Criteria:

  • being between 18-65 years old,
  • having unilateral or bilateral shoulder dysfunction,
  • ability to read and complete the self-assessment questionnaires

Exclusion Criteria:

  • have neurological, psychological and cardiovasculer diseases or injuries

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

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Objective and Subjective Items
Time Frame: 2 days
The Munich Shoulder Questionnaire is a 30-items self-assessment questionnaire. Its raw score ranges from 0 to 314. For comparability, the raw numbers are divided by 314 giving a percentage ranging from 0 to 100 in which higher scores represent a better function of the shoulder.
2 days

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Objective Function
Time Frame: 2 days
The objective function of the shoulder and consists of six items. The first five questions assess the range of motion: flexion, abduction, internal rotation, external rotation and range of the hand. Each question offer result from 0 to 10 points resulting in a total score ranging from a minimum of 0 to a maximum of 50 points ( 16 % of totals of MSQ) . The 6th targets at the power of the shoulder in 90° of abduction and 20° of quested to lift flexion. The patient is asked to fill a bag with items of daily living with a defined weıght such as a 500 gr water plastic bottle or bag. Then the patient is requested to lift the bag to the horizontal plane and hold 5 seconds. This is performed stepwise with increasing weights until the 12 kg. Each 500 gr is 2 point and maximum points is 24 for this question.(8%of the total MSQ).Altogether the objective part is a total score ranging from 0 to 74 points (%24 of the MSQ).
2 days
Subjective Function
Time Frame: 2 days
subjective function and consists of 24 items. Six of the items deal with pain, nine cover work and activities of daily living, six cover sports and recreation activities and three ask for the social and emotional quality of life. This section accounts for a total score ranging from 0 to 240 points (%76 of the MSQ). It raw score ranges from 0 to 314. For comparability, the raw numbers are divided by 314 giving a percentage ranging from 0 to 100 in which higher scores represent a better function of shoulder
2 days

Collaborators and Investigators

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

Collaborators

Investigators

  • Study Director: Gamze Ekici, Prof., Hacettepe University

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.

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 15, 2015

Primary Completion (Actual)

January 15, 2019

Study Completion (Actual)

April 15, 2019

Study Registration Dates

First Submitted

April 16, 2019

First Submitted That Met QC Criteria

May 17, 2019

First Posted (Actual)

May 20, 2019

Study Record Updates

Last Update Posted (Actual)

May 20, 2019

Last Update Submitted That Met QC Criteria

May 17, 2019

Last Verified

May 1, 2019

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Validation and Reability of the Munich Shoulder Questionnaire Into Turkish Patients

IPD Sharing Time Frame

3 months

IPD Sharing Access Criteria

18-65 years Having shoulder problem

IPD Sharing Supporting Information Type

  • SAP

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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