Neck Musculoskeletal Symptoms Among Turkish Endodontists
ENDO-NECK
Analysis of Neck Musculoskeletal Symptoms, Functional Parameters, and Associated Factors in Turkish Endodontists
1 other identifier
observational
120
1 country
1
Brief Summary
This observational study aims to evaluate the prevalence, severity, and characteristics of neck musculoskeletal symptoms among Turkish endodontists. Endodontists are exposed to prolonged static postures and repetitive movements during clinical procedures, which may increase the risk of neck-related disorders. Participants will be asked to complete questionnaires regarding demographic characteristics, occupational factors, ergonomic conditions, and neck pain. In addition, physical assessments including cervical range of motion, muscle strength, endurance, posture, and proprioception will be performed using validated measurement tools. The study also aims to identify factors associated with neck pain, such as working conditions, posture, and clinical experience. The findings may help improve preventive strategies, ergonomic recommendations, and rehabilitation approaches for dental professionals.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started May 2026
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 1, 2026
CompletedFirst Posted
Study publicly available on registry
April 8, 2026
CompletedStudy Start
First participant enrolled
May 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 1, 2027
April 8, 2026
April 1, 2026
1 year
April 1, 2026
April 1, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Prevalence and Severity of Neck Pain
Neck pain will be assessed using a self-reported questionnaire evaluating the presence, frequency, duration, and intensity of pain. Pain intensity will be measured using a numeric rating scale (0-10), where higher scores indicate greater pain severity.
Baseline
Secondary Outcomes (7)
Neck Disability Index (NDI) Score
Baseline
Cervical Range of Motion
Baseline
Cervical Isometric Muscle Strength
Baseline
Deep Cervical Flexor Muscle Endurance
Baseline
Cervical Postural Parameters
Baseline
- +2 more secondary outcomes
Study Arms (1)
Turkish Endodontists
Endodontists aged 25 to 65 years who are actively practicing in Turkey and voluntarily agree to participate in the study. Participants will complete questionnaires on demographic, occupational, ergonomic, and neck pain-related factors, and will undergo physical assessments including cervical range of motion, isometric muscle strength, muscle endurance, posture, proprioception, and neck disability evaluation. Participants may later be analyzed in subgroups according to occupational factors such as microscope use.
Interventions
This is an observational study with no therapeutic or experimental intervention. Participants will undergo questionnaire-based evaluations and physical assessments including cervical range of motion, muscle strength, endurance, posture, and proprioception measurements.
Eligibility Criteria
The study population consists of actively practicing endodontists in Turkey, aged 25 to 65 years, working in public institutions, university hospitals, or the private sector. Participants with and without neck pain will be included to evaluate neck musculoskeletal symptoms, functional parameters, and associated occupational and ergonomic factors.
You may qualify if:
- Aged 25 to 65 years
- Actively practicing as an endodontist in Turkey in public institutions, university hospitals, or the private sector
- Willing and able to provide informed consent
- Endodontists with or without neck pain
You may not qualify if:
- History of cervical spine surgery within the last 3 months
- History of cervical spine infection within the last 3 months (e.g., spondylodiscitis)
- History of malignancy involving the cervical region
- Spinal cord compression due to tumor or another cause
- Presence of neurological deficit
- Inflammatory disease involving the cervical region, such as rheumatoid arthritis
- Use of muscle relaxant medication within the last 1 week
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Atlas Universitylead
Study Sites (1)
University of Health Sciences, Haydarpasa Numune Training and Research Hospital
Istanbul, Uskudar, 34860, Turkey (Türkiye)
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 1, 2026
First Posted
April 8, 2026
Study Start
May 1, 2026
Primary Completion (Estimated)
May 1, 2027
Study Completion (Estimated)
August 1, 2027
Last Updated
April 8, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share
Individual participant data will not be shared due to privacy and confidentiality considerations, as well as the absence of prior participant consent for data sharing.