The Effect of Exercise and Ergonomics Training Program on Musculoskeletal Disorders in Teachers

March 2, 2026 updated by: Doç.Dr.Ömer Şevgin, Uskudar University

The Effect of Exercise and Ergonomics Training Program on Musculoskeletal Disorders in Teachers: A Randomized Controlled Trial

Comparing the effectiveness of ergonomics and exercise training given to teachers regarding musculoskeletal disorders.

Study Overview

Detailed Description

This study is planned as a randomized controlled experimental study. The research will be conducted with teachers working in schools affiliated with the Tatvan National Education Directorate. The study will evaluate the effect of a structured exercise program, given in conjunction with ergonomics training, on musculoskeletal disorders compared to the group that received only ergonomics training. The study population consists of teachers working in preschool, primary, secondary, and high school levels who have musculoskeletal disorders.

Pain intensity will be assessed using the Visual Analog Scale . The Oswestry Disability Index will be used to assess functional impairment due to lower back pain, and the Neck Disability Index will be used to assess functional impairment due to neck pain. The distribution and frequency of musculoskeletal symptoms according to body regions will be assessed using the Nordic Musculoskeletal Questionnaire, and the level of burnout will be assessed using the Maslach Burnout Inventory. All measurement tools will be applied before and after the intervention.

Study Type

Interventional

Enrollment (Estimated)

80

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

Study Locations

    • Tatvan
      • Bitlis, Tatvan, Turkey (Türkiye)
        • Recruiting
        • Tatvan
        • Contact:
          • Muharrem AKAR
          • Phone Number: +905075850626

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria

  • Being between 30-60 years old
  • Having been a teacher for at least 5 years
  • Having experienced musculoskeletal pain for at least three months
  • Being able to participate in the ergonomics training and exercise program planned during the study period

Exclusion Criteria

  • Having a pain score below 3 on the Visual Analog scale
  • Having a neurological or orthopedic disease that prevents exercise
  • Having undergone musculoskeletal surgery within the last six months
  • Having a psychological disorder that may prevent exercise

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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: control group
Teachers who will receive ergonomics training
Ergonomics training will be implemented in a total of four sessions, in weeks 1, 4, 8, and 12, and each session will last approximately 30-45 minutes. The training content will cover: posture awareness, classroom work ergonomics, computer and whiteboard use, standing work, lifting and carrying techniques, and ergonomic suggestions for daily life.
Experimental: exercise
Teachers will be given exercises along with ergonomics training.
Ergonomics training will be implemented in a total of four sessions, in weeks 1, 4, 8, and 12, and each session will last approximately 30-45 minutes. The training content will cover: posture awareness, classroom work ergonomics, computer and whiteboard use, standing work, lifting and carrying techniques, and ergonomic suggestions for daily life.
In addition to ergonomics training, participants in the experimental group will undergo a structured exercise program lasting approximately 35-45 minutes a day, 3 days a week, for 12 weeks. The exercise program will consist of stretching, strengthening, posture, and core stabilization exercises targeting the neck, shoulders, back, and lower back, and will be planned to progress in stages.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Maslach Burnout Scale
Time Frame: 14 weeks
The scale consists of 22 questions in total. A 5-point Likert scale is used to answer the questions. There are options such as 0- Never, 1- Rarely, 2- Sometimes, 3- Often, 4- Always. Volunteers are asked to tick the appropriate option for each question. The scale has 3 sub-categories. There are 9 items for the emotional exhaustion section, 5 items for the depersonalization section, and 8 items for the personal achievement section. People with high burnout levels are expected to have high scores on the emotional exhaustion section and depersonalization section, and low personal achievement scores. The scores that can be obtained from the subscales range from 0-36 for emotional exhaustion, 0-20 for depersonalization, and 0-32 for personal achievement.
14 weeks
Nordic Musculoskeletal Questionnaire
Time Frame: 14 weeks
It is a scale used to determine the extent of pain in the musculoskeletal system. The purpose of this questionnaire is to identify and compare pain and complaints in parts of the body. There is an image showing the 9 parts of the body included in the questionnaire. These body parts; neck, shoulders, back, elbows, hands, waist, hips, knees and feet. The respondents are asked whether they have experienced problems such as pain and discomfort in their body parts in the last 12 months, in the last 4 weeks, and on the day of the assessment, and they are asked to mark this as yes or no.
14 weeks
Oswestry Disability Index
Time Frame: 14 weeks
The Oswestry Disability Index (ODI) is a self-completed questionnaire used to assess the level of disability in patients with low back pain. In the current study, the ODI will be used to evaluate the impact of low back pain on patients' daily lives.The survey consists of ten sections focusing on different aspects of daily life, such as pain severity, personal care, weight lifting, walking, sitting, standing, sleep, sexual function, social life, and travel. Each section contains six statements scored from 0 to 5; The first expression is zero, indicating no disability. The scores of all questions are summed and then multiplied by two to obtain an index ranging from 0 to 100. The higher the score, the greater the disability.
14 weeks
Neck Disability Index
Time Frame: 14 weeks
it consist of 10 questions in total, including ones about pain intensity, personal care, lifting, reading, headaches, driving, concentration, work, sleeping, and recreation Each item is scored from 0 (no disability) to 5 (total disability)
14 weeks

Collaborators and Investigators

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

Investigators

  • Study Chair: Muharrem AKAR, Uskudar University

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 (Actual)

March 1, 2026

Primary Completion (Estimated)

June 15, 2026

Study Completion (Estimated)

August 30, 2026

Study Registration Dates

First Submitted

February 25, 2026

First Submitted That Met QC Criteria

February 25, 2026

First Posted (Actual)

March 2, 2026

Study Record Updates

Last Update Posted (Actual)

March 3, 2026

Last Update Submitted That Met QC Criteria

March 2, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

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

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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