- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05912361
Impact of Training Dental Students for an AI-Based Platform
The Impact of Training Dental Students for Using a Novel Artificial Intelligence-based Platform for Pulp Exposure Prediction Before Deep Caries Excavation: A Randomized Controlled Trial
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Copenhagen, Denmark, 2200
- University of Copenhagen Department of Odontology Cariology and Endodontics Section for Clinical Oral Microbiology
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- perhaps 4th year and 5th year dental students at the university of Copenhagen who are willing to participate voluntarily and have signed the consent letter.
- Limited or no previous knowledge and experience about AI
Exclusion Criteria:
- None
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Students using AI-platform for assessing the risk of pulp exposure receiving a training session
Students will go through a one-hour hands-on training session before taking the test at the online platform. The session includes a theoretical session related to basic aspects of AI in radiology, CNN (Convolutional Neural Network) applications for cariology and endodontics, as well as basics of excavation therapy and pulp exposure. the theoretical part will be followed by a hands on session on which participants check 11 cases of teeth with deep caries and will find the closest line between caries and pulp. Then, they will receive access to log in to the website on which pretreatment x-rays of cases undergoing caries excavation therapy is uploaded. The performance of students on will be assessed. |
The students at the experimental group will receive a one-hour hands-on training session before logging in to the online platform.
The session will be presented by a dentist with AI experience and this session will present basic aspects of AI in radiology, deep learning (DL) applications for cariology and endodontics, as well as basics of excavation therapy and pulp exposure.
the theoretical part will be followed by a hands on session on which each participant will check 11 cases of teeth with deep caries and will find the closest line between caries and pulp.
their performance will be supervised by the training session presenter and the correct line will be shown them in case of making wrong line.
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|
No Intervention: Students using AI-platform for assessing the risk of pulp exposure without any training session
Students will not receive any training before starting the experiment.
Only a 5-minute video will be played as the guide for answering the questions in the website.
Then, they will receive access to log in to the website on which pretreatment x-rays of cases undergoing caries excavation therapy is uploaded.
The performance of students on will be assessed.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Performance of students at pulp exposure prediction in the AI-based platform with and without training session based on their accuracy
Time Frame: 30 days
|
The accuracy of students at both group (with and without training session) will be measured and compared together.
The accuracy measurement for each student will be calculated by the number of correct predictions of pulp exposure occurrence divided by the total predictions.
|
30 days
|
|
Performance of students at pulp exposure prediction in the AI-based platform with and without training session based on their sensitivity
Time Frame: 30 days
|
The sensitivity of students at both group (with and without training session) will be measured and compared together.
It will be based on the proportion of actual pulp exposure cases that got predicted as pulp exposure (true positive).
|
30 days
|
|
Performance of students at pulp exposure prediction in the AI-based platform with and without training session based on their specificity
Time Frame: 30 days
|
The specificity of students at both group (with and without training session) will be measured and compared together.
It will be based on the proportion of actual 'no pulp exposure' cases correctly predicted as cases without pulp exposure (true negative).
|
30 days
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 504-0342/22-5000
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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