- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06947733
Analysis of the Effect of Pre-course Videos on Improving Clinical Skills in Emergency Ultrasound Training (CVC)
Project Background Point-of-Care Ultrasound (POCUS) has become an important part of medical education in recent years. However, due to limited resources of ultrasound machines and clinical instructors, hands-on practice opportunities are limited, affecting the quality of teaching. Effectively imparting ultrasound operation skills has become a major challenge in improving training quality. This project aims to evaluate the impact of pre-class videos on enhancing ultrasound teaching effectiveness, particularly comparing videos shot with a first-person perspective (POV) to those shot with a face-to-face perspective.
Project Objectives Primary Objective: To evaluate the impact of learning from pre-class videos on enhancing the effectiveness of ultrasound teaching.
Secondary Objective: To investigate the effect of different filming techniques (POV versus face-to-face) on learning outcomes.
Research Design The study will adopt a parallel research design, with subjects randomly assigned to one of three groups: the first-person perspective video group, the face-to-face perspective video group, and the control group (who will not watch any videos).
Procedure on the Day of Instruction Complete a basic information and learning experience questionnaire. Conduct a pre-test practical, recording the operation of the ultrasound. Provide one-on-one instruction, offering detailed operational guidance. Conduct a post-test practical, allowing students to independently perform ultrasound-guided central venous catheter insertion.
Complete a post-test questionnaire. Expected Outcomes This study anticipates that learning through pre-class videos will effectively enhance students' ultrasound operation skills and improve teaching quality. Teaching videos shot with a POV may provide a more realistic learning experience, thereby enhancing students' learning outcomes. By comparing different filming techniques, this project will provide empirical data that can inform future ultrasound teaching methods, ultimately improving the overall effectiveness of medical education.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Population Participants included PGY physicians at the hospital, the majority of whom had not previously performed independent CVC insertion or used ultrasound guidance. A total of 72 PGY physicians voluntarily enrolled in the study after receiving invitations via email and posters. No adverse events were reported during the study.
Video Preparation
Instructional videos were recorded in two formats:
First-person POV video using a GoPro mounted on the instructor's head.
Face-to-face (FtF) side-view video using two strategically placed cameras to capture side and front views simultaneously.
Both videos were standardized to 25 minutes and 42 seconds in duration and were uploaded privately on YouTube. Access was restricted to registered participant emails and granted three days prior to training. A cartoon character inserted at the end of each video served as a verification checkpoint during pre-class surveys.
Interventions
Participants were randomized into one of three groups using a block randomization method:
POV first-person video group
Face-to-face side-view video group
Control group (no video)
All participants received a pre-class email. The video groups received access to their assigned instructional video and the CVC checklist, while the control group received only the checklist.
Training Day Procedure
Participants first completed a pre-training questionnaire assessing demographics, procedural experience, and video viewing compliance. This was followed by:
Pre-training assessment: Participants performed ultrasound-guided CVC on a phantom model, evaluated by a competency checklist and global rating score.
One-on-one instruction: Instructors provided standardized guidance.
Post-training assessment: Participants repeated the CVC procedure independently and were re-evaluated.
Post-training questionnaire: Included self-assessed confidence and satisfaction scores.
All assessments were performed by a single instructor who was blinded to group allocation.
Statistical Analysis
Continuous variables were reported as medians with interquartile ranges, and categorical variables as counts and percentages. Normality was assessed, and non-parametric tests were used due to skewed data. Between-group comparisons were performed using:
Kruskal-Wallis test (three-group comparison)
Mann-Whitney U test (two-group comparison)
Wilcoxon signed-rank test (paired pre/post comparison)
Chi-square or Fisher's exact test was used for categorical data. A significance threshold of α = 0.05 was used, with Bonferroni correction applied (adjusted α = 0.0167). Analyses were conducted in Python (version 3.13).
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Taipei, Taiwan, 112
- Taipei Veterans General Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- PGY physicians
- Medical students
Exclusion Criteria:
- who refused the invitation of this learning project
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: the first-person perspective video group
Students will watch first-person point-of-view (POV) filmed videos and will complete both pre- and post-tests on the day of the course.
|
This project aims to evaluate the impact of pre-class videos on enhancing ultrasound teaching effectiveness, particularly comparing videos shot with a first-person perspective (POV) to those shot with a face-to-face perspective.
|
|
Active Comparator: the face-to-face perspective video group
Students will watch the face-to-face perspective filmed videos and will complete both pre- and post-tests on the day of the course.
|
This project aims to evaluate the impact of pre-class videos on enhancing ultrasound teaching effectiveness, particularly comparing videos shot with a first-person perspective (POV) to those shot with a face-to-face perspective.
|
|
Placebo Comparator: the control group (who will not watch any videos)
A control group without video viewing will also complete both pre- and post-tests on the day of the course.
|
the control group (who will not watch any videos)
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Checklist Completion Score (0-34 points)
Time Frame: 6 months
|
Objective evaluation of procedural steps during central venous catheterization, assessed using a standardized skills checklist.
|
6 months
|
|
Global Rating Score (1-10 scale)
Time Frame: 6 months
|
Instructor-assigned score reflecting overall procedural fluency and technical competence.
|
6 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Procedural Time (minutes)
Time Frame: 6 months
|
Total time taken to complete the procedure during pre- and post-training assessments.
Comparisons will be made between: Participants who received pre-class videos vs. those who did not (pre-test comparison)
|
6 months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Po-Hsiang Liao, MD, Department of Emergency Medicine, Taipei Veterans General Hospital
Study record dates
Study Major Dates
Study Start (Actual)
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
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2024 - 06 - 006B
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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