Effects of Cadaveric Training on Clinical Confidence in Upper Extremity Ultrasound-Guided Procedures (UECAD-USG)

Effects of Cadaveric Training on Clinical Confidence in Upper Extremity Ultrasound-Guided Procedures: A Prospective Cross-Sectional Study

This prospective observational study evaluates the effects of a structured cadaveric workshop on physicians' self-reported confidence in performing upper extremity ultrasound-guided procedures. The workshop consisted of theoretical instruction and supervised hands-on cadaveric practice focusing on shoulder, elbow, and wrist procedures. Confidence levels were assessed before and after the workshop using standardized questionnaires. The study also examined the influence of prior ultrasound experience, procedural volume, and academic seniority on baseline confidence and post-workshop improvement.

Study Overview

Detailed Description

Ultrasound-guided musculoskeletal procedures are increasingly used in daily clinical practice because they improve procedural accuracy and reduce complication risk. However, upper extremity procedures require advanced sonoanatomical knowledge and technical proficiency due to the proximity of neurovascular structures and anatomical variability. Cadaveric workshops provide a realistic educational environment in which physicians can improve probe handling, needle guidance, and procedural confidence before performing these procedures in clinical settings.

This study evaluated the effectiveness of a one-day cadaveric musculoskeletal ultrasonography workshop focused on upper extremity ultrasound-guided procedures. The workshop included theoretical lectures and supervised hands-on cadaveric practice involving shoulder, elbow, and wrist procedures. Participants completed pre- and post-workshop questionnaires assessing self-reported confidence levels.

The primary objective was to determine changes in procedural confidence following workshop participation. Secondary objectives included evaluating the effects of prior ultrasound training, years of musculoskeletal ultrasonography experience, procedural volume, and academic seniority on baseline confidence and confidence improvement after the course.

Study Type

Observational

Enrollment (Actual)

78

Contacts and Locations

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

Study Locations

    • Istanbul
      • Istanbul, Istanbul, Turkey (Türkiye)
        • Koç University School of Medicine

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
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Physicians and physical medicine and rehabilitation trainees participating in cadaveric musculoskeletal ultrasonography workshops focused on upper extremity ultrasound-guided procedures.

Description

Inclusion Criteria:

  • Physicians participating in the cadaveric musculoskeletal ultrasonography workshop
  • Willingness to complete pre- and post-workshop questionnaires
  • Age ≥18 years

Exclusion Criteria:

  • Failure to complete both pre- and post-workshop assessments
  • Withdrawal from the workshop before completion

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
Workshop Participants
Physicians participating in a cadaveric musculoskeletal ultrasonography workshop focused on upper extremity ultrasound-guided procedures involving the shoulder, elbow, and wrist.
Participants attended a structured one-day cadaveric musculoskeletal ultrasonography workshop consisting of theoretical lectures and supervised hands-on practice sessions. The workshop focused on upper extremity ultrasound-guided procedures involving the shoulder, elbow, and wrist. Participants practiced probe positioning, sonoanatomical identification, and needle guidance techniques on cadaveric specimens under direct supervision by experienced instructors.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Self-Reported Confidence for Upper Extremity Ultrasound-Guided Procedures
Time Frame: Immediately before and immediately after the workshop
Self-reported confidence scores for shoulder, elbow, and wrist ultrasound-guided procedures assessed using a 5-point Likert scale before and immediately after the cadaveric workshop.
Immediately before and immediately after the workshop

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Participant Satisfaction With the Educational Workshop
Time Frame: Immediately after the workshop
Participant ratings regarding workshop content, practical applications, educational quality, and organizational aspects assessed using post-workshop questionnaires.
Immediately after the workshop

Collaborators and Investigators

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

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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)

May 27, 2025

Primary Completion (Actual)

February 15, 2026

Study Completion (Actual)

February 15, 2026

Study Registration Dates

First Submitted

May 22, 2026

First Submitted That Met QC Criteria

May 22, 2026

First Posted (Actual)

May 29, 2026

Study Record Updates

Last Update Posted (Actual)

May 29, 2026

Last Update Submitted That Met QC Criteria

May 22, 2026

Last Verified

May 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

De-identified participant-level questionnaire data, including demographic characteristics, professional background information, and pre- and post-workshop confidence assessments, will be shared.

IPD Sharing Time Frame

Beginning 6 months after publication of the study results and continuing for 5 years following publication.

IPD Sharing Access Criteria

Access to de-identified participant-level data and supporting documents will be provided to qualified researchers who submit a methodologically sound research proposal. Data will be made available upon reasonable request to the corresponding author and may be used for educational or musculoskeletal ultrasonography research purposes.

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF

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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