Workplace Violence and Safety Perception Among ENT Physicians in Turkey

April 21, 2026 updated by: Sumeyra DOLUOGLU, Saglik Bilimleri Universitesi

Perceived Safety and Security Against Workplace Violence Among Otolaryngology-Head and Neck Surgery Physicians: A Multicenter Cross-Sectional Survey Study in Turkey

This multicenter, cross-sectional survey study aims to evaluate the perceived level of safety and security against workplace violence among otolaryngology-head and neck surgery (ENT-HNS) physicians in Turkey. The study investigates the association between exposure to workplace violence and perceived safety, as well as the adequacy of institutional support mechanisms. Data will be collected through an anonymous online questionnaire distributed nationwide. The findings are expected to contribute to awareness and the development of preventive strategies and institutional safety policies for healthcare professionals.

Study Overview

Detailed Description

Workplace violence against healthcare professionals represents a significant occupational hazard, particularly for physicians working in high-risk clinical settings. ENT-HNS physicians frequently encounter high patient volumes, emergency conditions, and invasive procedures, which may increase the risk of violent incidents.

This non-interventional, cross-sectional study will be conducted using an anonymous, online survey distributed to ENT-HNS specialists and residents across Turkey. The questionnaire includes demographic and professional characteristics, workload indicators, exposure to different types of workplace violence (verbal, physical, and threats), reporting behaviors, and perceived safety levels measured using the "Healthcare Professionals' Safety and Security Perception Scale Against Violence."

The study involves minimal risk, limited to possible psychological discomfort due to recalling prior experiences of violence. No identifying information will be collected, and all data will be stored securely. Results will be reported in aggregate form only.

Study Type

Observational

Enrollment (Estimated)

450

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
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Otolaryngology-Head and Neck Surgery (ENT-HNS) specialist and resident physicians aged 18 years or older working in Turkey who voluntarily participate in the study.

Description

Inclusion Criteria:

  • Licensed ENT-HNS specialist or resident physician
  • Aged 18 years or older
  • Willingness to participate and provide informed consent

Exclusion Criteria:

  • Physicians from other medical specialties
  • Surveys with more than 20% missing data

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
ENT Physicians
Otolaryngology-Head and Neck Surgery (ENT-HNS) specialist and resident physicians aged 18 years or older working in Turkey who voluntarily participate in the study.
An anonymous, web-based questionnaire administered via Google Forms to assess demographic characteristics, workload, exposure to workplace violence, reporting behaviors, and perceived safety against workplace violence using a validated safety perception scale.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Perceived Safety Score Against Workplace Violence
Time Frame: At survey completion (single time point, baseline assessment)

Total score obtained from the Healthcare Professionals' Safety and Security Perception Scale Against Violence, a self-administered questionnaire assessing perceived safety and security in the workplace.

The scale consists of items scored on a Likert-type scale, with a minimum score of 0 and a maximum score of 10.

Higher scores indicate a higher perceived level of safety and security against workplace violence.

At survey completion (single time point, baseline assessment)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number of Participants Reporting Exposure to Workplace Violence
Time Frame: At survey completion (single time point, baseline assessment)
Self-reported exposure to workplace violence, categorized as verbal violence, physical violence, and threats, assessed using a structured questionnaire developed for this study.
At survey completion (single time point, baseline assessment)
Correlation Between Perceived Safety Score and Exposure to Workplace Violence
Time Frame: At survey completion (single time point, baseline assessment)

Correlation between:

Perceived Safety Score measured by the Healthcare Professionals' Safety and Security Perception Scale Against Violence (continuous total score, range 0-10), and

Exposure to workplace violence (yes/no), assessed via self-reported questionnaire.

At survey completion (single time point, baseline assessment)

Collaborators and Investigators

This is where you will find people and organizations involved with this 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 (Estimated)

April 2, 2026

Primary Completion (Estimated)

June 1, 2026

Study Completion (Estimated)

September 1, 2026

Study Registration Dates

First Submitted

December 16, 2025

First Submitted That Met QC Criteria

December 29, 2025

First Posted (Actual)

December 31, 2025

Study Record Updates

Last Update Posted (Actual)

April 22, 2026

Last Update Submitted That Met QC Criteria

April 21, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • Sumeyra Doluoglu (Other Identifier: University of Health Sciences, Ankara Etlik City Hospital)

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Individual participant data will not be shared.

De-identified data may be available from the corresponding investigator upon reasonable request, subject to ethics committee approval.

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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