Turkish Validity and Reliability of Short-Western Ontario Rotator Cuff Disability Index
Examination of the Validity and Reliability of the Short-Western Ontario Rotator Cuff Disability Index in Turkish in Patients With Rotator Cuff Injury
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The reliability and validity of the scale will begin with language equivalence and cultural adaptation. The scale will be translated from English to Turkish by two people who are fluent in Turkish and English. A single Turkish translation will be obtained from these two Turkish translations with a common opinion.
The scale, which has been translated into Turkish, will be translated into English by two other people who are fluent in Turkish and English. The scale translated into English will be compared with the original. In the pre-trial phase, a reassessment will be conducted with 15 participants to test the intelligibility of the scale. Based on the results of the pre-test phase, the final version of SHORTWORC will be able to be modified. The data of SHORTWORC are collecting through face-to-face when the patients came to the rehabilitation center. 35 participants will be included in the study.
In order to evaluate the validity of the SHORTWORC, the Western Ontario Rotator Cuff Disability Index (WORC), which can evaluate the quality of life in patients with rotator cuff injury and has been validated in Turkish, and the University of California-Los Angeles (UCLA) shoulder scale, which can evaluate the functionality of shoulder and has been validated in Turkish, will be used. Scales will be repeated after 15 days to assess test-retest reliability.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Istanbul, Turkey (Türkiye), 34720
- İstanbul Medeniyet University
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Istanbul, Turkey (Türkiye)
- İstanbul Medeniyet University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Individuals over 18 years of age who have been diagnosed with a rotator cuff injury,
- Patients whose native language is Turkish,
- Individuals with pain intensity > 2 according to the Visual Analog Scale,
- Individuals with a Mini Mental State Examination score of >24,
Exclusion Criteria:
- Individuals with pain and disability due to any shoulder pathology other than rotator cuff injury,
- Individuals who cannot read or write Turkish,
- Individuals with shoulder fractures, surgical interventions and other accompanying shoulder pathologies,
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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patients with Rotator cuff injury
Patients with roatator cuff injury who are aged over 18 years
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The aim of this study is to adapt the Short-Western Ontario Rotator Cuff Disability Index (SHORTWORC) to Turkish society in patients with rotator cuff injury and to make its validity and reliability in Turkish.
It has 7 questions.
The patients will be sought to answer questionnaires during regular rehabilitation sessions.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Disability
Time Frame: baseline
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Disability will be assessed with the Short-Western Ontario Rotator Cuff Disability Index (SHORTWORC) in patients with rotator cuff injury.
It haf 7 items.
Each item is scored on a 0-to-100-mm visual analog scale, summing a total score ranging from 0 (best possible score) to 700 (worst possible score).
Higher scores indicate poorer quality of life.
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baseline
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Functionality of shoulder
Time Frame: baseline
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Functionality of shoulder will be assessed with the University of California-Los Angeles (UCLA) shoulder scale.
It contains a total of 5 questions belonging to 5 categories: Pain (scored from 1-10), Function (scored from 1-10), range of motion (scored from 0-5), muscle strength (scored from 0-5), patient satisfaction (scored from 0-5).
Each category is scored differently.
Higher scores indicate better shoulder functionality.
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baseline
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- SHORTWORC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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