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RecruitingNCT07873567Updated Oct 14, 2026

Musculoskeletal Discomfort and Ergonomic Factors in Midwifery Students

An observational study in Musculoskeletal Discomfort, Ergonomic Risk Perception and Protective Ergonomic Behaviours, sponsored by Mardin Artuklu University. Recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-14.

Sponsored by Mardin Artuklu University · Observational

From the registry’s dates

  • Started Aug 2026; still recruiting 2 months later.
Updated Oct 14, 2026Newly registeredGo to Updates ↓
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
323
Ages
18 Years and older
Sex
All
01

Study summary

The aim of this observational study is to assess regional musculoskeletal discomfort, ergonomic risk perception, and protective ergonomic behaviors among undergraduate midwifery students at Mardin Artuklu University, Türkiye. The study will also examine the relationship between clinical task exposure and regional musculoskeletal discomfort among students with clinical practice experience.

Participants will complete a single online survey covering demographic and academic characteristics, musculoskeletal discomfort, ergonomic risk perception, protective ergonomic behaviors, physical activity, sleep quality, and trait anxiety. Students with clinical practice experience will additionally answer questions about their exposure to specific clinical tasks and postures. No intervention will be administered.

Read the detailed description

This cross-sectional observational study will recruit undergraduate midwifery students aged 18 years or older at Mardin Artuklu University, Türkiye. Participants will provide electronic informed consent and complete a single online survey.

Regional musculoskeletal discomfort will be assessed using the Turkish version of the Cornell Musculoskeletal Discomfort Questionnaire. Researcher-developed items will assess ergonomic risk perception and protective ergonomic behaviors. Students with clinical practice experience will additionally report their exposure to specific clinical tasks and postures during the preceding four weeks of clinical practice. Physical activity, sleep quality, and trait anxiety will be assessed using the International Physical Activity Questionnaire-Short Form, Pittsburgh Sleep Quality Index, and Trait Anxiety subscale of the State-Trait Anxiety Inventory, respectively.

Musculoskeletal discomfort will be compared across academic years. Associations with ergonomic risk perception and protective ergonomic behaviors will be examined while accounting for academic year, body mass index, physical activity, sleep quality, and trait anxiety. Associations between clinical task exposure and regional discomfort will be explored among students with clinical practice experience.

02

Conditions studied

  • Musculoskeletal Discomfort
  • Ergonomic Risk Perception
  • Protective Ergonomic Behaviours
  • Clinical Task Exposure

Keywords

  • midwifery students
  • ergonomics
  • musculoskeletal discomfort
  • physical activity
  • sleep quality
  • anxiety
03

In context

Motor Activity

2,646 studies on the registry are indexed under Motor Activity; 1,205 are open to participants now.

This study's planned enrollment of 323 is above the median of 100 across 318 observational studies indexed under Motor Activity.

Browse Motor Activity studies →

Lead sponsor

Mardin Artuklu University is the lead sponsor of 32 studies on the registry; 13 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Undergraduate midwifery students aged 18 years or older enrolled in the Faculty of Health Sciences at Mardin Artuklu University, Türkiye. All eligible students across academic years will be invited to participate in the online survey. Clinical task exposure will be assessed only among students with clinical practice experience.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Enrolled in the undergraduate midwifery program at Mardin Artuklu University.
  • Aged 18 years or older.
  • Able to read and understand Turkish.
  • Willing to participate and provide electronic informed consent.

Exclusion criteria

Exclusion Criteria:

  • Incomplete responses to the main sections of the survey.
  • Serious trauma, fracture, or surgery within the preceding six months that could directly affect musculoskeletal symptoms.
  • A self-reported health condition preventing completion of the questionnaires.
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
323 participants (estimated)
Patient registry
No

Groups and cohorts

  • Undergraduate Midwifery Students

    Undergraduate midwifery students aged 18 years or older enrolled at Mardin Artuklu University, Türkiye, who provide electronic informed consent and complete an online survey. Clinical task exposure will be assessed only among students with clinical practice experience.

06

What researchers measure

Primary outcomes

  1. Musculoskeletal Discomfort Assessed by the Cornell Musculoskeletal Discomfort Questionnaire

    The Turkish version of the Cornell Musculoskeletal Discomfort Questionnaire will be used to assess the frequency, severity, and interference with work or activities of musculoskeletal discomfort during the preceding week. Regional scores will be calculated by multiplying the frequency, severity, and interference scores, and the total score will be calculated by summing regional scores. Higher scores indicate greater musculoskeletal discomfort.

    Time frame: At enrollment (single assessment)

Secondary outcomes

  1. Ergonomic Risk Perception

    Ten researcher-developed items will be used to assess perceived ergonomic risks associated with academic and clinical tasks and postures. Each item is rated from 0 (not risky) to 4 (very risky). The mean item score ranges from 0 to 4, with higher scores indicating greater perceived ergonomic risk. This is a study-specific descriptive index.

    Time frame: At enrollment (single assessment)

  2. Protective Ergonomic Behaviours

    Eight researcher-developed items will be used to assess the frequency of protective ergonomic behaviors during academic and clinical activities. Each item is rated from 0 (never) to 4 (always). The mean item score ranges from 0 to 4, with higher scores indicating more frequent protective ergonomic behaviors. This is a study-specific descriptive index.

    Time frame: At enrollment (single assessment)

  3. Clinical Task Exposure

    Ten researcher-developed items will be used to assess exposure to specific clinical tasks and postures during the preceding four weeks of clinical practice. Each item is rated from 0 (never) to 4 (very frequently). Item scores will be evaluated separately, with higher scores indicating more frequent exposure. This measure will be assessed only among students with clinical practice experience.

    Time frame: At enrollment (single assessment)

  4. Physical Activity Level

    The Turkish version of the International Physical Activity Questionnaire-Short Form will be used to assess walking, moderate-intensity activity, and vigorous-intensity activity during the preceding seven days. Total physical activity will be expressed in metabolic equivalent minutes per week (MET-min/week), with higher values indicating greater physical activity. Participants will also be classified into low, moderate, or high physical activity categories according to the scoring guidelines.

    Time frame: At enrollment (single assessment)

  5. Sleep Quality

    The Turkish version of the Pittsburgh Sleep Quality Index will be used to assess sleep quality during the preceding month. Seven component scores, each ranging from 0 to 3, will be summed to obtain a global score ranging from 0 to 21. Higher scores indicate poorer sleep quality. A global score greater than 5 indicates poor sleep quality.

    Time frame: At enrollment (single assessment)

  6. Trait Anxiety Assessed by the State-Trait Anxiety Inventory

    The Turkish version of the Trait Anxiety subscale of the State-Trait Anxiety Inventory (STAI) will be used to assess participants' general tendency to experience anxiety. The subscale contains 20 items rated on a four-point scale. Total scores range from 20 to 80, with higher scores indicating greater trait anxiety.

    Time frame: At enrollment (single assessment)

07

Study locations

1 of 1 sites recruiting
  • Mardin Artuklu University Faculty of Health Sciences
    Mardin, 47000, Turkey (Türkiye)
    Recruiting
08

References and documents

Individual participant data

Plan to share: No — There is no plan to share individual participant data. Findings will be disseminated in aggregate form through scientific publications.

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Registered
First appeared on the registry. No changes since
Oct 14, 2026
Show all 1 update
  1. Oct 14, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07873567
Lead sponsor
Mardin Artuklu University
Responsible party
Emrullah Alkan (Assistant Professor, Mardin Artuklu University) — Principal investigator
First posted
Oct 14, 2026
Start date
Aug 1, 2026
Primary completion
Nov 5, 2026 (estimated)
Completion
Nov 25, 2026 (estimated)
Last update
Oct 14, 2026

Study contacts

Emrullah Alkan, PhD
Contact
emrullahalkan@artuklu.edu.tr
+904822134002
İlke Kara Öz, PhD Candidate
Contact
ilke.kara@deu.edu.tr
+902324124907
Emrullah Alkan, PhD
principal investigator · Mardin Artuklu University
İlke Kara Öz, PhD Candidate
principal investigator · Dokuz Eylul University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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