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Clinical Trials/NCT05760365
NCT05760365RecruitingNot Applicable

The Improvement of Medical Education by Using the Application of Three-dimensional Printing in Cardiac Catheterization

Fu Jen Catholic University2 sites in 1 country50 target enrollmentStarted: October 2, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
50
Locations
2
Primary Endpoint
Examination score of pre-intervention

Study Overview

Brief Summary

Our purpose is to use 3D printing technology to make human anatomical cardiovascular model, which could apply in the medical education for medical students, in order to improve the effectiveness of the learning process to access.

Detailed Description

Background:

The medical teaching models are expansive and rare. We try to use the 3D printing technology to print cardiovascular model. By using the 3D cardiovascular model, we try to facilitate the leaning curve of understanding the cardiac catheterization.

Study Design:

This is a single-site prospective randomized controlled trial of medical education. We expect to enrolled 50 participants. Both group will receive same teaching program. Traditional education model will be used in control group, and 3D printed model will be used in the experimental group.

Methods:

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Other
Masking
Single (Investigator)

Eligibility Criteria

Ages
20 Years to 50 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Medical student, nurse practitioner and Resident in Fu Jen Catholic University Hospital

Exclusion Criteria

  • Refused to participate in the study.

Arms & Interventions

Slide-based presention group

Active Comparator

Received a regular learning

Intervention: Slide-based presention (Other)

3D-printed presention group

Experimental

Received a regular learning plus 3D printing model

Intervention: 3D printed educational model (Other)

Outcomes

Primary Outcomes

Examination score of pre-intervention

Time Frame: pre-intervention

score of pre-intervention (maximun 100 and minimum 0), higher means a better outcome

Examination score of post-intervention

Time Frame: immediately after the intervention

score of post-intervention (maximun 100 and minimum 0), higher means a better outcome

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Ke-Yun, Chao

Group leader of Respiratory Therapists

Fu Jen Catholic University

Study Sites (2)

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