- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06862401
Sequential Practicing on Psychomotor Skill Acquisition in Undergraduate Dental Students (Dentalpractice)
March 27, 2025 updated by: Nareudee Limpuangthip, DDS, PhD, Chulalongkorn University
Influence of Sequential Practicing for Psychomotor Skill Acquisition of Non-dominant Hand in Undergraduate Dental Students: A Randomized Controlled Trial With Qualitative Approach
To determine the influence of hand practice sequence on psychomotor skill acquisition in a glass ceramic onlay preparation among undergraduate dental students.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
Effect of bilateral transfer practice on psychomotor skill acquisition among dental students remains unresolved.
Bilateral transfer assumed that training one side of the body can also improve performance on the other side.
Eligible participants are fourth- to sixth-year undergraduate dental students at the Faculty of Dentistry, Chulalongkorn University during the 2024 to 2025 academic year.
The participants were categorized as left- or right-handed based on self-reporting.
Participants enrolled two-day study with one-week separating inverval.
On the first day, they learn a video presentation on glass ceramic onlay preparation followed by two practice sessions with 2-hour within each session.
The practice start with either using non-dominant or dominant hand, followed by the use of non-dominant hand.
One week later, they enroll two-hour practical examination on glass ceramic onlay preparation using their non-dominant hand.
No practice is allowed during one-week separating interval.
Study Type
Interventional
Enrollment (Estimated)
28
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Nareudee Limpuangthip, DDS, PhD
- Phone Number: +66891426076
- Email: Nareudee.L@chula.ac.th
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- The fourth- to sixth-year undergraduate dental students at a single setting of school
- The fifth- and sixth-year students had completed laboratory and lecture courses in operative and fixed dental prosthodontics
- The fourth-year students are enrolled in their final laboratory and lecture courses in fixed prosthodontics.
Exclusion Criteria:
Undergraduate dental students who have prior experience with onlay preparation in laboratory or clinical settings or those who are unwillingness to adhere to the study protocol.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
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: Left: dominant - non dominant
The left-handed participants in this arm started practicing a tooth preparation for a glass ceramic onlay using their dominant left hand during the first practicing session, followed by non-dominant right hand during the second practicing session.
Each practice session is limited to 2 hours.
|
The participants engaged in two practice sessions, each lasting two hours.
They either started with their dominant hand followed by non-dominant hand or practiced solely with their non-dominant hand.
Each participant prepared a mandibular left first molar resin typodont fixed to the table for a glass ceramic onlay restoration.
Preparation was conducted extraorally.
|
|
Active Comparator: Left: non dominant
The left-handed participants in this arm practicing a tooth preparation for a glass ceramic onlay using their non-dominant right hand for both the first and second practicing sessions.
Each practice session is limited to 2 hours.
|
The participants engaged in two practice sessions, each lasting two hours.
They either started with their dominant hand followed by non-dominant hand or practiced solely with their non-dominant hand.
Each participant prepared a mandibular left first molar resin typodont fixed to the table for a glass ceramic onlay restoration.
Preparation was conducted extraorally.
|
|
Experimental: Right: dominant - non dominant
The right-handed participants in this arm started practicing a tooth preparation for a glass ceramic onlay using their dominant right hand during the first practicing session, followed by non-dominant left hand during the second practicing session.
Each practice session is limited to 2 hours.
|
The participants engaged in two practice sessions, each lasting two hours.
They either started with their dominant hand followed by non-dominant hand or practiced solely with their non-dominant hand.
Each participant prepared a mandibular left first molar resin typodont fixed to the table for a glass ceramic onlay restoration.
Preparation was conducted extraorally.
|
|
Active Comparator: Right: non dominant
The right-handed participants in this arm practicing tooth preparation for glass ceramic onlay using their non-dominant left hand for both the first and second practicing sessions.
Each practice session is limited to 2 hours.
|
The participants engaged in two practice sessions, each lasting two hours.
They either started with their dominant hand followed by non-dominant hand or practiced solely with their non-dominant hand.
Each participant prepared a mandibular left first molar resin typodont fixed to the table for a glass ceramic onlay restoration.
Preparation was conducted extraorally.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Onlay preparation score
Time Frame: 3 hours
|
Onlay preparation criteria using Rubic scale, assessed by the student self-assessment and one prosthodontic staff.
The higher score indicates better performance of the student
|
3 hours
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Qualitative measurement by focus group interview
Time Frame: 1 hours
|
Focus group interview based on the semi-structural questionnaire regarding individual perception on the onlay preparation during practice and test sessions.
|
1 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Nareudee Limpuangthip, DDS, PhD, Chulalongkorn University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
March 31, 2025
Primary Completion (Estimated)
May 30, 2025
Study Completion (Estimated)
July 4, 2025
Study Registration Dates
First Submitted
March 2, 2025
First Submitted That Met QC Criteria
March 2, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
April 2, 2025
Last Update Submitted That Met QC Criteria
March 27, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- TCTR20241210005
- Thai Clinical Trial.org (Other Identifier: Thai Clinical Trials Registry (TCTR))
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
The enrolled participants would not prefer to declare their onlay preparation score individually.
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
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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