- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06553079
Development of the Surgeon Satisfaction Self-Assessment Questionnaire for Shoulder Arthroscopy
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The "Surgeon Satisfaction Self-Assessment Questionnaire for Shoulder Arthroscopy" is being developed to address the need for a standardized tool to evaluate surgeon satisfaction in the context of shoulder arthroscopy. This study is structured into two primary phases: survey development and validation.
Phase 1: Survey Development In the initial phase, semi-structured interviews will be conducted with a diverse group of surgeons who specialize in shoulder arthroscopy. These interviews will explore various dimensions of surgical satisfaction, including technical factors, patient outcomes, surgical equipment performance, and team dynamics. The qualitative data obtained from these interviews will be analyzed to identify recurring themes and factors that are crucial to surgeon satisfaction. Based on these findings, a draft questionnaire will be developed, ensuring that it comprehensively covers all relevant aspects of the surgical experience.
Phase 2: Validation Process Once the questionnaire is drafted, it will undergo a rigorous validation process. Content validity will be established by consulting with a panel of experts in orthopedic surgery and psychometrics to ensure that the questionnaire items are both relevant and exhaustive. Construct validity will be tested using factor analysis to determine the underlying structure of the questionnaire and to ensure it accurately measures the intended constructs of satisfaction. Criterion validity will be assessed by comparing the questionnaire outcomes with established benchmarks or other validated tools. Additionally, the questionnaire's reliability will be evaluated through test-retest and internal consistency measures Cronbach's alpha.
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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-
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Ankara, Turkey, 06500
- Gazi University Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Orthopedic Surgeons:Must be a licensed orthopedic surgeon actively performing shoulder arthroscopy procedures.
- Participants must be willing to provide informed consent and participate in both the questionnaire development (including interviews) and the validation phases of the study.
- Participants must be proficient in the language in which the questionnaire is administered to ensure accurate and meaningful responses.
Exclusion Criteria:
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Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Surgeons Performing Shoulder Arthroscopy
This is the main group of interest and includes surgeons who regularly perform shoulder arthroscopy.
They will be the primary respondents to the survey and will provide insights into the factors affecting their surgical satisfaction.
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The intervention in this study involves the administration of the "Surgeon Satisfaction Self-Assessment Questionnaire for Shoulder Arthroscopy," a newly developed tool designed to measure various aspects of surgeon satisfaction related to shoulder arthroscopy procedures.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Validation of the Surgeon Satisfaction Self-Assessment Questionnaire for Shoulder Arthroscopy
Time Frame: 6 months
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The primary outcome measure is the successful development and psychometric validation of the Surgeon Satisfaction Self-Assessment Questionnaire for Shoulder Arthroscopy.
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6 months
|
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
- Iayas11
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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