Postural and Muscle Fatigue Analysis of Endodontic Residents

February 20, 2024 updated by: Díaz-Flores García, Universidad Europea de Madrid

Postural and Muscle Fatigue Analysis of Endodontic Residents: A Research Proposal

Musculoskeletal disorders (MSDs) are a significant occupational health problem for dentists and have been linked to a decline in quality of life, often leading to stress-related illnesses and early retirement. Poor posture, poor movement or imbalances in the neck or shoulders can lead to the three most common pain syndromes in dentistry. The objectives of this study were to evaluate the working position adopted during an endodontic procedure and to determine the perception of symptoms of musculoskeletal disorders in first and second year students of the Master in Advanced Endodontics at the European University of Madrid (UEM), using the standardised Nordic Kuorinka questionnaire supplemented by a form with socio-demographic variables. This study has a descriptive cross-sectional observational design and included 10 students selected by convenience sampling. A video camera was used to record the procedures from three different angles for a maximum of 5 minutes. The information was processed using Microsoft Excel spreadsheet software, and the video recordings were assessed using Rodgers' Muscular Fatigue Analysis (RMFA) and Rapid Upper Limb Assessment (RULA).

Study Overview

Detailed Description

The unit of analysis for this study consisted of the first and second year students of the Master's in Endodontics programme at the European University of Madrid (UEM) who completed the two years of annual clinical practice during the years 2022/24. A total of 10 students were enrolled over the two years of training, treating 30 patients (3 patients per student) in the first year and another 30 patients in the second year (for a total of 22 months). A video camera was used to record the procedures from three different angles for a maximum of 5 minutes (two side views - right and left - and one frontal view) on different patients, following the National Institute for Occupational Safety and Health (NIOSH) Protocol for Video Recording for Job Analysis and Risk Assessment. The selected endodontic procedure focused exclusively on upper or lower first molars during the opening and ultrasonic search for the fourth canal in upper first molars or the search for the mesiobuccal canal in lower first molars. The standardised Nordic Kuorinka Musculoskeletal Symptom Perception Questionnaire was used as the measuring instrument. Questionnaire data were collected using a spreadsheet program (Microsoft Excel).

Study Type

Observational

Enrollment (Estimated)

10

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

Study Contact Backup

Study Locations

    • Madrid
      • Villaviciosa De Odón, Madrid, Spain
        • Recruiting
        • Universidad Europea de Madrid
        • Contact:
          • Antonio Conde, PhD

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

Sampling Method

Non-Probability Sample

Study Population

1st and 2nd year students of the Master's Degree in Endodontics of the European University of Madrid (UEM), who have completed the two years of the annual teaching period of clinical practice during the years 2022/24.

Description

Inclusion Criteria:

- Students of the Master's Degree in Endodontics of the European University of Madrid (UEM), who have completed the two years of the annual teaching period of clinical practice.

Exclusion Criteria:

  • Subjects previously diagnosed with a musculoskeletal disorder.
  • Subjects who had suffered previous trauma affecting the musculoskeletal system.
  • Pregnant women in their third trimester.
  • Subjects who refused to participate.

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
Group 1
1st Year Students
Group 2
2nd year students

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Symptom Perception
Time Frame: January 2023 - July 2024
The standardized Nordic Kuorinka Musculoskeletal Symptom Perception Questionnaire will be used as a measurement instrument. Data from the questionnaires will be compiled in a spreadsheet program (Microsoft Excel); measures of central tendency and dispersion will be calculated as well as tables and figures. Sociodemographic variables such as age, sex, grade, weight, height, symptoms of musculoskeletal disorders, body regions affected and times of symptom onset will be recorded.
January 2023 - July 2024

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Ruth Perez Alfayate, PHD, Universidad Europea de Madrid

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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 (Estimated)

April 30, 2024

Primary Completion (Estimated)

June 30, 2025

Study Completion (Estimated)

November 1, 2025

Study Registration Dates

First Submitted

February 2, 2024

First Submitted That Met QC Criteria

February 20, 2024

First Posted (Actual)

February 28, 2024

Study Record Updates

Last Update Posted (Actual)

February 28, 2024

Last Update Submitted That Met QC Criteria

February 20, 2024

Last Verified

February 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

The data obtained will be used for scientific publications.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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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