Development of the Surgeon Satisfaction Self-Assessment Questionnaire for Shoulder Arthroscopy

August 10, 2024 updated by: İnci Hazal Ayas, Gazi University
This observational study aims to develop and validate the "Surgeon Satisfaction Self-Assessment Questionnaire for Shoulder Arthroscopy." The study involves conducting in-depth interviews with surgeons who perform shoulder arthroscopy to identify key factors influencing their surgical satisfaction, including individual, patient-related, and surgical equipment-related factors. Based on the insights gained from these interviews, a comprehensive questionnaire will be developed. The questionnaire will then undergo validation processes, including assessments of content, construct, criterion, and reliability, to ensure it accurately and consistently measures surgeon satisfaction. The final validated tool is intended to provide a reliable method for surgeons to self-assess their satisfaction with shoulder arthroscopy procedures, contributing to improved surgical practices and outcomes.

Study Overview

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

Observational

Enrollment (Estimated)

30

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, 06500
        • Gazi University Hospital

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

The study population consists of orthopedic surgeons who specialize in shoulder arthroscopy and are actively engaged in performing these procedures. Participants will be recruited from a variety of clinical settings, including academic medical centers, private practices, and specialized orthopedic clinics. The surgeons included in the study will have diverse levels of experience, ranging from early-career surgeons with low practice to highly experienced surgeons with decades of experience in the field.

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:

-

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

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.
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.

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
The primary outcome measure is the successful development and psychometric validation of the Surgeon Satisfaction Self-Assessment Questionnaire for Shoulder Arthroscopy.
6 months

Collaborators and Investigators

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

Sponsor

Investigators

  • Study Director: Ulunay Kanatlı, Professor, Gazi University

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 (Estimated)

September 1, 2024

Primary Completion (Estimated)

December 1, 2024

Study Completion (Estimated)

March 1, 2025

Study Registration Dates

First Submitted

August 10, 2024

First Submitted That Met QC Criteria

August 10, 2024

First Posted (Actual)

August 14, 2024

Study Record Updates

Last Update Posted (Actual)

August 14, 2024

Last Update Submitted That Met QC Criteria

August 10, 2024

Last Verified

August 1, 2024

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

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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