NCT06061003

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.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
98

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Sep 2023

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

September 24, 2023

Completed
5 days until next milestone

First Posted

Study publicly available on registry

September 29, 2023

Completed
Same day until next milestone

Study Start

First participant enrolled

September 29, 2023

Completed
2.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 29, 2025

Completed
1 day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 30, 2025

Completed
Last Updated

May 28, 2025

Status Verified

May 1, 2025

Enrollment Period

2.1 years

First QC Date

September 24, 2023

Last Update Submit

May 27, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Clinical Test

    A 25-question multiple choice questions 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.

    one hour

Secondary Outcomes (3)

  • Academic Motivation

    one hour

  • Test Anxiety Inventory

    one hour

  • Enjoyment and Ease of Use Assessment

    one hour

Study Arms (2)

Fractured Model Group

OTHER

All participants will receive 60 minutes training on anatomy and pathophysiology of theoric wrist fractures. After lecture completed, the Fractured Model Group will engage in a 2-hours hands-on practical session in the laboratory, working with wrist fracture models.

Other: Clinical Anatomical Education with Fractured Bone Models

Standard Anatomic Model Group

OTHER

All participants will receive 60 minutes training on anatomy and pathophysiology of theoric wrist fractures.After lecture completed, the Standard Anatomic Model Group will engage in a 2-hours hands-on practical session in the laboratory, working with standard anatomical wrist models.

Other: Clinical Anatomical Education with Standard Bone Models

Interventions

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.

Fractured Model Group

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.

Standard Anatomic Model Group

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • having stereopsis above 40 arc/seconds according to the Titmus Stereopsis Test

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Abant Izzet Baysal University

Bolu, Merkez, 14100, Turkey (Türkiye)

RECRUITING

Related Publications (1)

  • Kurul R, Inal B, Diramali M, Ozer H, Erdogan KE. Evaluating the educational impact of tomography-based high-resolution 3D-printed distal radius fracture models. BMC Med Educ. 2025 Dec 24;25(1):1706. doi: 10.1186/s12909-025-08164-w.

MeSH Terms

Conditions

Pathological Conditions, Anatomical

Condition Hierarchy (Ancestors)

Pathological Conditions, Signs and Symptoms

Study Officials

  • Ramazan Kurul

    Abant Izzet Baysal University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Muhammed NUR OGUN, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
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.
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: Two groups as intervention and control groups. Assessments will be performed before intervention, and after the theorical/practical lectures.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assist. Prof

Study Record Dates

First Submitted

September 24, 2023

First Posted

September 29, 2023

Study Start

September 29, 2023

Primary Completion

October 29, 2025

Study Completion

October 30, 2025

Last Updated

May 28, 2025

Record last verified: 2025-05

Data Sharing

IPD Sharing
Will not share

Locations