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

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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