Validity And Reliability Study Of The Turkish Version Of Short Western Ontario Rotator Cuff Index

October 31, 2023 updated by: Selda Başar, Gazi University
The purpose of this study is to examine the psychometric properties of a Turkish shortened version of the Western Ontario Rotator Cuff Index (SHORTWORC).

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

Many of the musculoskeletal diseases that doctors treat every day affect both quality of life and functionality. Rotator Cuff diseases are highly prevalent shoulder disorders associated with pain and functional limitations. Thus, surveys measuring treatment outcomes and activity limitations have become important in clinical research. Such scales can be time consuming or impractical for the patient, depending on the areas they evaluate. For this reason, the development of scales focusing on specific areas facilitates evaluations in the clinical environment. The purpose of this study is to examine the psychometric properties the Turkish SHORTWORC index, which is designed to focus on a single parameter.

Study Type

Observational

Enrollment (Estimated)

75

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Ankara, Turkey, 06560
        • Recruiting
        • Gazi University
        • Contact:

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

  • Adult

Accepts Healthy Volunteers

No

Sampling Method

Probability Sample

Study Population

İndividuals diagnosed with Rotator cuff disease by a specialist in Gazi University Faculty of Medicine Orthopedics and Traumatology Polyclinic constitute the sample of the study.

Description

Inclusion Criteria:

  • Between the ages of 18-64
  • the presence of rotator cuff pathology requiring surgical treatment

Exclusion Criteria:

  • Chronic inflammatory diseases
  • cervical spine radiculopathy
  • different structural shoulder problems in the last three months
  • previous surgery and associated additional pathologies requiring stabilization or other major *surgery such as superior labral repair
  • any history of systemic disease
  • being an athlete

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
Short Western Ontario Rotator Cuff Index
Time Frame: First Day
The scale of Short Western Ontario Rotator Cuff Index is a disease-spesific index designed to evaluate activity limitations in patient with rotator cuff disorders. It is an abbreviated version of Western Ontario Rotator Cuff Index (WORC). İt has 7 items that access only 1 domain , the activity limitations. Patients rate their function on a scale from 0, meaning no difficulty, to 100, meaning extreme difficulty. The percentage scores for the Short-WORC are obtained by subtracting the total score from 700, dividing by 700, and multiplying by 100, resulting in a total percentage score varying from 0 to 100.,
First Day
Constant-Murley score (CMS)
Time Frame: First Day
The Constant-Murley score (CMS) is a 100-points scale composed of a number of individual parameter. These parameters define the level of pain and the ability to carry out the normal daily activities of the patient. The Constant-Murley score was introduced to determine the functionality after the treatment of a shoulder injury.
First Day
American Shoulder and Elbow Surgeons Shoulder Score (ASES)
Time Frame: First Day
The ASES is a 100-point scale that consists of two dimensions: pain and activities of daily living. There is one pain scale worth 50 points and ten activities of daily living worth 50 points. İt has been also reported to be reliable and valid in patients ,with upper extremity, shoulder or rotator cuff pathology.
First Day

Collaborators and Investigators

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

Sponsor

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)

September 1, 2023

Primary Completion (Estimated)

November 1, 2023

Study Completion (Estimated)

December 1, 2023

Study Registration Dates

First Submitted

October 19, 2023

First Submitted That Met QC Criteria

October 31, 2023

First Posted (Actual)

November 1, 2023

Study Record Updates

Last Update Posted (Actual)

November 1, 2023

Last Update Submitted That Met QC Criteria

October 31, 2023

Last Verified

October 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 2023-1070

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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