- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06799585
Dental Loupes in Pediatric Dentistry Practice Affect Ergonomic Posture (ergonomy)
January 23, 2025 updated by: DİLARA NİL GÜNAÇAR, Recep Tayyip Erdogan University Training and Research Hospital
Does Wearing Dental Loupes in Pediatric Dentistry Practice Affect Ergonomic Posture?
This study aims to investigate the effect of wearing DL on the working posture of pediatric dentists.
Study Overview
Status
Completed
Detailed Description
In pulpotomy procedures performed with DL in 23 patients and without DL in 23 patients, photographs will taken at a total of 3 times in each patient: at the beginning of the procedure, 15th and 30th minutes.
The working postures of the clinicians will analyzed using the Modified-Dental Operator Posture Assessment Instrument (M-DOPAI) method through these photographs.
Study Type
Observational
Enrollment (Actual)
46
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ri̇ze
-
Lütfen Seçiniz, Ri̇ze, Turkey, 53100
- Recep Tayyip Erdogan University Faculty of Dentistry
-
-
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
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Pediatric population
Description
Inclusion Criteria:
- indication for pulpotomy in the mandibular right second primary molar,
- 3 (positive)- 4 (definitely positive) according to the Frankl Behavior Scale,
- parents volunteered to participate in the study and signed the informed consent form,
- did not have any systemic disease or disability.
Exclusion Criteria:
- contraindication for pulpotomy in the mandibular right second primary molar
- 2 (negative)- 1 (definitely negative) according to the Frankl Behavior Scale
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
Cohorts and Interventions
Group / Cohort |
|---|
|
pulpotomy procedures performed with Dental Loupe
Treatment appointments were set to be at the first hour of the day to ensure standardization for each patient.
The physicians worked with the same patient chair, physician chair, and DL.
|
|
pulpotomy procedures performed without Dental Loupe
Treatment appointments were set to be at the first hour of the day to ensure standardization for each patient.
The physicians worked with the same patient chair, physician chair, without DL.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
The effect of wearing DL on the working posture with Modified-Dental Operator Posture Assessment Instrument (M-DOPAI)
Time Frame: 3 month
|
3 month
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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 (Actual)
January 2, 2024
Primary Completion (Actual)
January 1, 2025
Study Completion (Actual)
January 15, 2025
Study Registration Dates
First Submitted
January 23, 2025
First Submitted That Met QC Criteria
January 23, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
January 23, 2025
Last Verified
January 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2023/251
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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