Violence in ICU: Outcomes, Lessons, and Experiences of ICU Team (The VIOLENT-Study)
Investigating Management and Perceptions of Aggression, Conflict, and Threat in ICU Environments
1 other identifier
observational
500
1 country
1
Brief Summary
This study aims to investigate the perceptions, experiences, and responses of healthcare professionals working in intensive care units in Switzerland concerning patient violence.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Mar 2025
Shorter than P25 for all trials
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
Study Start
First participant enrolled
March 1, 2025
CompletedFirst Submitted
Initial submission to the registry
March 20, 2025
CompletedFirst Posted
Study publicly available on registry
April 10, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2025
CompletedApril 10, 2025
April 1, 2025
9 months
March 20, 2025
April 7, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (12)
Demographic information (ICU Staff Questionnaire)
Participants provide demographic details, including gender and age, using a questionnaire.
2025
Completion date (ICU Staff Questionnaire)
The date of questionnaire completion is recorded.
2025
Professional background (ICU Staff Questionnaire)
Assessment of professional role of the intensive care unit (ICU) staff, including their education and work experience, using a questionnaire.
2025
Frequency of violent incident (ICU Staff Questionnaire)
Participants report the frequency of violent incidents encountered from patients or their relatives in the ICU setting, using a questionnaire.
2025
Type of violent incident (ICU Staff Questionnaire)
Participants report the type of violent incidents (verbal, physical, and sexual) encountered from patients or their relatives in the ICU setting, using a questionnaire.
2025
Characteristics of violent incident (ICU Staff Questionnaire)
Participants provide detailed information about specific violent incidents they have experienced in the ICU, including the context and perceived triggers, using a questionnaire.
2025
Reporting of violent incident (ICU Staff Questionnaire)
Participants report whether the violent incident has been reported, using a questionnaire.
2025
Personal impact of workplace violence (ICU Staff Questionnaire)
Participants describe the personal impact of workplace violence, including psychological and mental health consequences, using a questionnaire.
2025
Professional impact of workplace violence (ICU Staff Questionnaire)
Participants report how workplace violence influences professional factors such as job satisfaction and workload, using a questionnaire.
2025
Actions taken during or after violent incident (ICU Staff Questionnaire)
Participants report the responses and measures taken during or after the violent incident, using a questionnaire.
2025
Strategies for enhancing workplace safety in the ICU (ICU Staff Questionnaire)
Participants provide information on strategies for enhancing workplace safety in the ICU, such as existing institutional policies, prior training in handling workplace violence, and their opinions on workplace violence prevention and recommendations for enhancing ICU safety, using a questionnaire.
2025
Open-ended feedback from participant (ICU Staff Questionnaire)
Participants have the opportunity to share additional comments or remarks related to workplace violence and safety in the ICU, using a questionnaire. This information is collected through a freetext field in the questionnaire.
2025
Eligibility Criteria
Nurses and physicians working in the intensive care unit at Swiss hospitals
You may qualify if:
- Consenting nurses and physicians currently working in Swiss intensive care units
- Nurses and physicians consenting to participate will be included
You may not qualify if:
- Nurses and physicians who do not consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University Hospital Basel, Intensive Care Unit
Basel, Canton of Basel-City, 4031, Switzerland
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Raoul Sutter, Prof. Dr. med.
University Hospital Basel, Department of Acute Medicine, Intensive Care Unit
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 20, 2025
First Posted
April 10, 2025
Study Start
March 1, 2025
Primary Completion
December 1, 2025
Study Completion
December 1, 2025
Last Updated
April 10, 2025
Record last verified: 2025-04