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Work-related InjuryNCT07442409

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

A study testing Other: Standardized Ergonomics Training and Other: Standardized Ergonomics Training Plus Structured Exercise Programme in people with Work-related Injury and Work-related Illness, run by Uskudar University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 25 to 60 years, women onlyHealthy volunteers can take part
Conditions the study is for
Work-related Injury, Work-related Illness
What is being tested?
Other: Standardized Ergonomics Training and Other: Standardized Ergonomics Training Plus Structured Exercise Programme
Could I receive a placebo?
No, everyone receives an active treatment
How many people
50 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Mar 2026to 20 Jul 2026
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 25 to 60 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Female sex
  • Age 25-60 years
  • Actively engaged in dairy milking for at least 5 years
  • Sufficient physical capacity to participate in the education and exercise programme
  • Provision of written informed consent

Who cannot join

  • Any diagnosed concomitant musculoskeletal or rheumatological disease affecting any body region, including diagnosed wrist/hand conditions such as carpal tunnel syndrome or tendinopathy
  • Any concomitant neurological disease or neurological dysfunction
  • History of surgery involving the musculoskeletal system
  • Any serious systemic disease that would preclude participation

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Tatvan

    Istanbul

Other trials in Turkey (Türkiye)

About this study

Official title: 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.

Read the 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.

Being tested
Other: Standardized Ergonomics Training, Other: Standardized Ergonomics Training Plus Structured Exercise Programme

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Other: Standardized Ergonomics TrainingOther

    The control group will be given standard ergonomics training which includes proper body mechanics, correct working posture and musculoskeletal protection principles during milking.

  • Other: Standardized Ergonomics Training Plus Structured Exercise ProgrammeOther

    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.

Study groups in NCT07442409
Study groupRoleWhat they receive
Ergonomics TrainingActive comparatorParticipants receive three individual face-to-face ergonomics training sessions of approximately 60 minutes each at baseline and at the end of weeks 4 and 8. Training addresses appropriate body mechanics, working posture during milking, stool and equipment positioning, load handling, work-rest organization, wrist positioning and musculoskeletal protection. Participants also receive an illustrated brochure and telephone contact every two weeks.
Receives: Other: Other: Standardized Ergonomics Training
Ergonomics Training Plus Structured ExerciseExperimentalParticipants receive the same ergonomics training as the control group plus a 12-week home-based, equipment-free structured exercise programme performed three non-consecutive days per week. Each session lasts approximately 45-50 minutes and includes warm-up, stretching, postural and scapular control exercises, and progressive calisthenic strengthening exercises.
Receives: Other: Other: Standardized Ergonomics Training; Other: Other: Standardized Ergonomics Training Plus Structured Exercise Programme

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Work-Related Musculoskeletal Pain Intensity Assessed With the Visual Analogue Scale

    Pain intensity is assessed using a Visual Analogue Scale ranging from 0 to 10, where 0 indicates no pain and 10 indicates unbearable pain. Participants rate their overall work-related musculoskeletal pain considering the neck, shoulders, and lower back. Higher scores indicate greater pain intensity.

    Measured: Baseline (week 0) and post-intervention (week 12)

Secondary outcomes (4)
  1. Change in Upper-Limb Functional Disability Assessed With the QuickDASH

    The QuickDASH is an 11-item questionnaire scored from 0 to 100. Higher scores indicate greater upper-limb disability.

    Measured: Baseline (week 0) and post-intervention (week 12)

  2. Change in Depressive Symptoms Assessed With the Beck Depression Inventory

    Depressive symptoms are assessed with the Beck Depression Inventory. Higher total scores indicate greater depressive symptom severity.

    Measured: Baseline (week 0) and post-intervention (week 12)

  3. Change in Quality of Life Assessed With the WHOQOL-BREF

    Quality of life is assessed using the WHOQOL-BREF. The physical health, psychological health, social relationships, and environment domains are scored and transformed to a 4-20 scale. Higher scores indicate better quality of life.

    Measured: Baseline (week 0) and post-intervention (week 12)

  4. Musculoskeletal Symptom Prevalence Assessed With the Nordic Musculoskeletal Questionnaire

    The Standardised Nordic Musculoskeletal Questionnaire assesses musculoskeletal symptoms in nine body regions: neck, shoulders, upper back, elbows, wrists/hands, lower back, hips/thighs, knees, and ankles/feet. At baseline, the 12-month recall section is used; at week 12, the 7-day recall section is used. Results are reported descriptively because the recall periods differ between assessments.

    Measured: Baseline (12-month recall) and week 12 (7-day recall)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Mar 2026
  2. Study start1 Mar 2026
  3. Primary completion10 Jun 2026
  4. Study completion20 Jul 2026

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
50 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07442409
Sponsor's protocol ID
Uskudar94
Status last verified
Sep 2026
First submitted
25 Feb 2026
Last updated
9 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Das B. Work-related musculoskeletal disorders in agriculture: Ergonomics risk assessment and its prevention among Indian farmers. Work. 2023;76(1):225-241. doi: 10.3233/WOR-220246.

    PubMed 36806533
  • Kaewdok T, Sirisawasd S, Taptagaporn S. Agricultural Risk Factors Related Musculoskeletal Disorders among Older Farmers in Pathum Thani Province, Thailand. J Agromedicine. 2021 Apr;26(2):185-192. doi: 10.1080/1059924X.2020.1795029. Epub 2020 Jul 31.

    PubMed 32735182
  • Akbar KA, Try P, Viwattanakulvanid P, Kallawicha K. Work-Related Musculoskeletal Disorders Among Farmers in the Southeast Asia Region: A Systematic Review. Saf Health Work. 2023 Sep;14(3):243-249. doi: 10.1016/j.shaw.2023.05.001. Epub 2023 May 13.

    PubMed 37818214

Questions about this trial

What is this clinical trial studying?

A study testing Other: Standardized Ergonomics Training and Other: Standardized Ergonomics Training Plus Structured Exercise Programme in people with Work-related Injury and Work-related Illness, run by Uskudar University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 9 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Work-Related Musculoskeletal Pain Intensity Assessed With the Visual Analogue Scale (time frame: Baseline (week 0) and post-intervention (week 12)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07442409, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Sep 2026.

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