The Effect of Ergonomics and Exercise Training on Musculoskeletal Disorders in Female Dairy Farmers

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

The Effect of Ergonomics and Exercise Training on Musculoskeletal Disorders in Female Dairy Farmers: A Randomized Controlled Trial

The aim of this research is to comparatively examine the effects of ergonomics training and the combined application of ergonomics and structured exercise training on work-related musculoskeletal disorders in female farmers actively engaged in milking.

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

The study will assign female farmers actively engaged in milking to two groups using a simple randomization method: a control group (ergonomics training) and an experimental group (ergonomics and exercise training). The control group will receive standard ergonomics training aimed at reducing ergonomic risk factors encountered during milking. The experimental group will receive the same ergonomics training as the control group, plus a structured exercise program consisting of stretching, strengthening, and posture exercises. The exercise program will be planned based on progressive loading principles, muscle group-specific exercise selection, set-repetition arrangement, and standardization of rest intervals. The intervention period is 12 weeks, with exercises performed 3 days a week. All participants will be evaluated before and after the intervention using the Visual Analog Scale, Nordic Musculoskeletal Questionnaire, Quick Disabilities of the Arm, Shoulder and Hand, and the World Health Organization Quality of Life Short Form, all within the same assessment protocol.

Study Type

Interventional

Enrollment (Estimated)

60

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

  • Having been actively engaged in farming for at least 5 years
  • Being between 25-50 years of age
  • Being female
  • Having the physical ability to participate in the planned training and exercise program during the study period

Exclusion Criteria

  • Having any accompanying neurological disease or neurological dysfunction
  • Having a history of any musculoskeletal surgery
  • Having a serious systemic disease that may prevent the implementation of 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: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: control group
only the group that will receive ergonomics training
The control group will be given standard ergonomics training which includes proper body mechanics, correct working posture and musculoskeletal protection principles during milking.
Experimental: exercise group
The group will receive exercises along with ergonomics training.
The control group will be given standard ergonomics training which includes proper body mechanics, correct working posture and musculoskeletal protection principles during milking.
The exercise group will receive the same ergonomics training as well as a structured exercise program consisting of stretching, strengthening and posture exercises. The exercise program will be planned to last three days a week for a total of 12 weeks.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
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
QuickDASH
Time Frame: 14 weeks
QuickDASH score of the mobility of the arm, shoulder, hand and its function by using the QuickDASH questionnaire. The QuickDASH is scored in two components: the disability/symptom section (11 items, scored 1-5) and the optional high performance sport/music or work modules (4 items, scored 1-5). A higher score indicates greater disability.
14 weeks
Beck Depression Inventory
Time Frame: 14 weeks
The Beck Depression Inventory is a 21-question multiple-choice self-report inventory for measuring the severity of depression. Higher total scores indicate more severe depressive symptoms. The range of scores vary from 0 to 63 (highest possible total) for the whole test. A score of 0 - 10 indicates minimal depression, while a score of over 40 indicates extreme depression. No subscales were used for this outcome.
14 weeks
World Health Organization Quality of Life (Brief)
Time Frame: 14 weeks
The World Health Organization Quality of Life brief is a 16 item quality of life scale covering four domains of QOL. Each item is scored from 1-5 with higher response employing a higher quality of life.
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 30, 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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