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
1 other identifier
observational
40
1 country
2
Brief Summary
The aim of this study is to adapt the Short-Western Ontario Rotator Cuff Disability Index (SHORTWORC) to Turkish society and to make its validity and reliability in Turkish. The Western Ontario Rotator Cuff Disability Index (WORC) developed by Kirkley et al assesses quality of life in patients with Rotator Cuff İnjury. The WORC has 21 questions. The WORC was shortened and renamed as Short-Western Ontario Rotator Cuff Disability Index (SHORTWORC). The SHORTWORC consists of 7 questions. This study will be conducted with patients with rotator cuff injuries. The patients will be sought to answer questionnaires during regular rehabilitation sessions. 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 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Oct 2024
Shorter than P25 for all trials
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
October 4, 2024
CompletedFirst Posted
Study publicly available on registry
October 8, 2024
CompletedStudy Start
First participant enrolled
October 20, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 20, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2025
CompletedSeptember 2, 2025
August 1, 2025
2 months
October 4, 2024
August 25, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Disability
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.
baseline
Secondary Outcomes (1)
Functionality of shoulder
baseline
Study Arms (1)
patients with Rotator cuff injury
Patients with roatator cuff injury who are aged over 18 years
Interventions
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.
Eligibility Criteria
Patients with rotator cuff injury who are aged over 18 years
You may qualify if:
- 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,
You may not qualify if:
- 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,
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
İstanbul Medeniyet University
Istanbul, 34720, Turkey (Türkiye)
Istanbul Medeniyet University
Istanbul, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Target Duration
- 15 Days
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Research Assistant
Study Record Dates
First Submitted
October 4, 2024
First Posted
October 8, 2024
Study Start
October 20, 2024
Primary Completion
December 20, 2024
Study Completion
April 30, 2025
Last Updated
September 2, 2025
Record last verified: 2025-08
Data Sharing
- IPD Sharing
- Will not share