NCT06630039

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Oct 2024

Shorter than P25 for all trials

Geographic Reach
1 country

2 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 4, 2024

Completed
4 days until next milestone

First Posted

Study publicly available on registry

October 8, 2024

Completed
12 days until next milestone

Study Start

First participant enrolled

October 20, 2024

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 20, 2024

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 30, 2025

Completed
Last Updated

September 2, 2025

Status Verified

August 1, 2025

Enrollment Period

2 months

First QC Date

October 4, 2024

Last Update Submit

August 25, 2025

Conditions

Keywords

roatator cuff injuriesscale validitypain

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

Other: Scale validity and reliability

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.

patients with Rotator cuff injury

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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)

Location

Istanbul Medeniyet University

Istanbul, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Rotator Cuff InjuriesPain

Condition Hierarchy (Ancestors)

RuptureWounds and InjuriesShoulder InjuriesTendon InjuriesNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

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

Locations