NCT06567236

Brief Summary

Based on pilot study's promising results, we decided to further investigate the impact of adapting Planmeca Romexis Compare software to evaluate pulpal access preparations on second-year dental students' technical performance, self-evaluation skills and opinions. No educational records, grades, coursework, or any other assignments that are completed as part of the regular class will be analyzed as part of this study.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
59

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Feb 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Study Start

First participant enrolled

February 27, 2023

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 8, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 8, 2023

Completed
1.3 years until next milestone

First Submitted

Initial submission to the registry

August 19, 2024

Completed
3 days until next milestone

First Posted

Study publicly available on registry

August 22, 2024

Completed
Last Updated

August 22, 2024

Status Verified

August 1, 2024

Enrollment Period

2 months

First QC Date

August 19, 2024

Last Update Submit

August 21, 2024

Conditions

Keywords

EndodonticsPredental educationEducational technologyTeaching methods

Outcome Measures

Primary Outcomes (2)

  • Self-assessment - traditional method vs traditional method plus 3D software method

    Compare self-assessment after traditional method only and with extra 3D software method

    baseline, 2 weeks, 4 weeks, 5 weeks and 7 weeks

  • Grading - traditional method vs traditional method plus 3D software method

    Compare technical skills after traditional method only and with extra 3D software method

    baseline, 2 weeks, 4 weeks, 5 weeks and 7 weeks

Secondary Outcomes (1)

  • Grading - traditional/visual grading vs 3D software grading

    baseline, 2 weeks, 4 weeks, 5 weeks and 7 weeks

Study Arms (2)

Traditional teaching method

NO INTERVENTION

Participants will be exposed to traditional teaching method.

3D software teaching method.

EXPERIMENTAL

Participants will be exposed to traditional teaching method and 3D software teaching method.

Other: 3D software

Interventions

Participants in the experimental arm will receive extra training on Planmeca Romexis Compare Software adapted to evaluate endodontic access preparation.

3D software teaching method.

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Second-year dental students enrolled in DDDS 719 Integrated Practice of Dentistry Lab II during 2022-2023 at Texas A\&M School of Dentistry
  • Students who have completed fixed prosthodontics preclinical course
  • Students attending the endodontics preclinical course.

You may not qualify if:

  • First, third and fourth-year dental students at Texas A\&M School of Dentistry
  • Second-year dental students NOT enrolled in DDDS 719 Integrated Practice of Dentistry Lab II during 2022-2023 at Texas A\&M School of Dentistry
  • Students who are not interested in participating.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Texas A&M School of Dentistry

Dallas, Texas, 75246, United States

Location

Related Publications (1)

  • Poly A, Burnett JE, Buie CA, Schweitzer JL. Three-dimensional software adapted to evaluate endodontic access cavity preparation. J Dent Educ. 2023 Dec;87 Suppl 3:1848-1851. doi: 10.1002/jdd.13216. Epub 2023 Apr 11. No abstract available.

    PMID: 37016471BACKGROUND

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 19, 2024

First Posted

August 22, 2024

Study Start

February 27, 2023

Primary Completion

May 8, 2023

Study Completion

May 8, 2023

Last Updated

August 22, 2024

Record last verified: 2024-08

Data Sharing

IPD Sharing
Will not share

Locations