3D Resin Printed Fracture Models for Anatomy Education

Sponsor
Abant Izzet Baysal University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06061003
Collaborator
(none)
90
1
2
1.5
59.6

Study Details

Study Description

Brief Summary

Resin printing is an emerging technology with a wide array of applications. This research seeks to assess the practicality of incorporating 3D resin printed models into anatomy education while investigating how fractured models impact students' decision-making and quiz scores.

Condition or Disease Intervention/Treatment Phase
  • Other: Clinical Anatomical Education with Fractured Bone Models
  • Other: Clinical Anatomical Education with Standard Bone Models
N/A

Detailed Description

Over the past decade, 3D printing has become increasingly accessible and cost-effective, offering systems and materials suitable for home use. 3D printing is a technology that streamlines production by translating computer-generated models into physical objects, layer by layer. In comparison to other tissue engineering and rapid prototyping methods, 3D printing boasts numerous advantages, such as exceptional precision, rapid production, cost-effectiveness, and seamless integration. Utilizing 3D models can significantly enhance the comprehension of intricate structures for medical professionals and students alike. Common materials used in 3D printing include robust nylon, aluminum, gypsum, textile components, polylactic acid, and resin. Among these, photosensitive resin stands out, as it enables the creation of higher-quality, more intricate structures that closely resemble real tissues, offering a smoother finish devoid of visible raw material textures.

This study's primary objective was to assess the suitability of tissues produced by a 3D resin printer in anatomy education, with the aim of enhancing hands-on training through direct manipulation of fractured bone models.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
90 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Two groups as intervention and control groups. Assessments will be performed before intervention, and after the theorical/practical lectures.Two groups as intervention and control groups. Assessments will be performed before intervention, and after the theorical/practical lectures.
Masking:
Single (Outcomes Assessor)
Masking Description:
Due to the study design, control group will not receive any fractured models for practical lectures therefore only outcome assessor will be blinded to group allocation.
Primary Purpose:
Other
Official Title:
Can High Resolution 3D Resin Printed Models be Used in Clinical Anatomy Education for Fracture Rehabilitation
Anticipated Study Start Date :
Sep 30, 2023
Anticipated Primary Completion Date :
Oct 30, 2023
Anticipated Study Completion Date :
Nov 15, 2023

Arms and Interventions

Arm Intervention/Treatment
Other: Fractured Model Group

All participants will receive 1 hour training on anatomy and pathophysiology of toric wrist fractures. After lecture completed, the Fractured Model Group will engage in a 1-hour hands-on practical session in the laboratory, working with wrist fracture models.

Other: Clinical Anatomical Education with Fractured Bone Models
Participants will undergo a 2-hour training session, consisting of 60 minutes of theory and 60 minutes of practice. The theoretical lesson, supported by 2D images illustrating wrist anatomy, types of fractures, and rehabilitation based on fracture type, will be simultaneously delivered to both groups. Following this, the practical group will receive a 60-minute hands-on session using 3D-printed digital models of radius and ulna fractures. These training sessions will be scheduled in the morning hours, on a day when students have no other classes between 9 am and 12 pm, to minimize mental fatigue and exhaustion. In the practical session, anatomical structures, their relationships, and arrangements will be demonstrated to the practice group using a model of a fractured wrist.

Other: Standard Anatomic Model Group

All participants will receive 1 hour training on anatomy and pathophysiology of toric wrist fractures.After lecture completed, the Standard Anatomic Model Group will engage in a 1-hour hands-on practical session in the laboratory, working with standard anatomical wrist models.

Other: Clinical Anatomical Education with Standard Bone Models
Participants will undergo a 2-hour training session, consisting of 60 minutes of theory and 60 minutes of practice. The theoretical lesson, supported by 2D images illustrating wrist anatomy, types of fractures, and rehabilitation based on fracture type, will be simultaneously delivered to both groups. Following this, the practical group will receive a 60-minute hands-on session using 3D-printed digital models of radius and ulna fractures. These training sessions will be scheduled in the morning hours, on a day when students have no other classes between 9 am and 12 pm, to minimize mental fatigue and exhaustion. The control group will receive the same practical session using a standard anatomical model.

Outcome Measures

Primary Outcome Measures

  1. Clinical Test [one hour]

    A 30-question test will be employed to assess students' anatomical knowledge and their decision-making capabilities for the rehabilitation program. The test will be prepared according to Bloom's taxonomy and will consist of both multiple-choice and open-ended questions. Total test time wil lbe 60 minutes and scores will be recorded as percentages.

Secondary Outcome Measures

  1. Academic Motivation Scale [one hour]

    Academic Motivation Scale will be used to assess participants' motivations. This scale, consisting of 28 questions and 7 subscales, evaluates amotivation, as well as internal and external motivation.

  2. Test Anxiety Inventory [one hour]

    To examine whether there is a change in the level of anxiety experienced by students during the exam, a 20-question Test Anxiety Inventory will be used. The test includes sections related to ease, comfort associated with learning, and alignment of exam questions with the course.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 40 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • having stereopsis above 40 arc/seconds according to the Titmus Stereopsis Test
Exclusion Criteria:
  • having partial or total vision loss

  • having a history of traumatic injury to the upper extremities within the last six months

  • having used wrist anatomy models in virtual or real environments

Contacts and Locations

Locations

Site City State Country Postal Code
1 Abant Izzet Baysal University Bolu Merkez Turkey 14100

Sponsors and Collaborators

  • Abant Izzet Baysal University

Investigators

  • Principal Investigator: Ramazan Kurul, Abant Izzet Baysal University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ramazan KURUL, Assist. Prof, Abant Izzet Baysal University
ClinicalTrials.gov Identifier:
NCT06061003
Other Study ID Numbers:
  • AIBU-FTR-RK-08
First Posted:
Sep 29, 2023
Last Update Posted:
Sep 29, 2023
Last Verified:
Sep 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 29, 2023