- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06553092
Turkish Validity and Reliability Study of Hospital for Special Surgery Shoulder Surgery Expectations Survey
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The process begins with the translation of the original survey into Turkish, followed by a back-translation to ensure accuracy. The adapted survey is then reviewed by a panel of experts to confirm its cultural relevance and clarity.
Once finalized, the Turkish version of the survey is administered to a cohort of Turkish-speaking patients who have undergone shoulder surgery. Participants complete the survey at a designated time point, typically postoperatively, to assess their expectations and outcomes related to the surgery. The collected data are then analyzed to evaluate the survey's reliability (internal consistency, test-retest reliability) and validity (content, construct, and criterion validity) within this specific population.
The goal of the intervention is to ensure that the Turkish version of the survey is a reliable and valid tool for assessing patient expectations and satisfaction following shoulder surgery, making it suitable for use in clinical practice and research in Turkey.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: İnci H Ayas, Msc
- Phone Number: (0312) 216 26 01
- Email: inciayass@gmail.com
Study Locations
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Ankara, Turkey, 06500
- Gazi University Hospital
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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:
- Underwent Shoulder Surgery
- Native Turkish Speakers
- Adults (18 years and older)
- Consent to Participate
Exclusion Criteria:
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Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
urkish-Speaking Patients Undergoing Shoulder Surgery
This cohort consists of Turkish-speaking patients who have undergone shoulder surgery.
Participants will complete the Turkish version of the Hospital for Special Surgery Shoulder Surgery Expectations Survey.
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The Hospital for Special Surgery (HSS) Shoulder Surgery Expectations Survey is a patient-reported outcome measure designed to assess a patient's expectations before undergoing shoulder surgery.
It helps clinicians understand what patients anticipate regarding pain relief, functional improvement, and overall recovery from the procedure.The HSS Shoulder Surgery Expectations Survey contains 20 questions.
Each question addresses a specific aspect of shoulder function or a potential outcome that patients might expect from their surgery.Each question is scored between 1-5.It is evaluated out of a total of 80 points.
A higher score indicates a greater expectation of improvement.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Validity and Reliability of the Turkish Version of the Hospital for Special Surgery Shoulder Surgery Expectations Survey
Time Frame: 6 months
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The primary outcome measure is to evaluate the psychometric properties of the Turkish version of the Hospital for Special Surgery Shoulder Surgery Expectations Survey.
This includes assessing the survey's internal consistency, test-retest reliability, content validity, construct validity, and criterion validity in a cohort of Turkish-speaking patients who have undergone shoulder surgery.
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6 months
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Collaborators and Investigators
Sponsor
Investigators
- Study Director: Ulunay Kanatlı, Professor, Gazi University
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Iayas12
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
product manufactured in and exported from the U.S.
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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