Actively Recruiting
Effect of Suicide Prevention Training for Professionals on Knowledge and Attitudes Regarding Suicide Prevention
Led by University Ghent · Updated on 2023-12-06
10000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the effect of suicide prevention trainings on the knowledge and attitudes of professionals in Flanders. These trainings target intermediaries such as caregivers, teachers, and police officers, aiming to improve their skills and confidence in handling suicidal individuals and crisis situations. While previous studies show these trainings can be effective, this research focuses on assessing their impact specifically in Flanders. Participants will take part in a one-arm trial where they receive a suicide prevention training organized by the Centre for the Prevention of Suicide and suicide prevention workers from the Centers for Mental Health Care. The trainings are announced publicly or organized on demand. All participants who register will be invited to complete online questionnaires at three time points: one week before the training (pre-test), immediately after the training (post-test, within 3 days), and three months after the training (follow-up). During the study, participants will complete questionnaires to assess changes in their knowledge, attitudes, and responses related to suicide prevention. The primary outcome is the change in knowledge and attitudes from before the training to after and at follow-up. Researchers will also measure how participants' responses to suicidal situations change over time. The study includes follow-up monitoring for three months after the training to evaluate lasting effects.
CONDITIONS
Brief Title
Effect of Suicide Prevention Training for Professionals
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participating in a suicide prevention training organised by 'Centrum ter Preventie van Zelfdoding' or 'Su�fcicidepreventiewerking Centra Geestelijke Gezondheidszorg'
You will not qualify if you...
- Not participating in a suicide prevention training organised by 'Centrum ter Preventie van Zelfdoding' or 'Su�fcicidepreventiewerking Centra Geestelijke Gezondheidszorg'
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit (in-person or online)
Duration - 1 day
Participants receive a suicide prevention training provided by the Centre for the Prevention of Suicide and related organizations.
1 training session visit
Duration - 3 months
Participants are followed up to assess changes in knowledge, attitudes, and responses to suicide prevention after training.
1 follow-up visit (in-person or online)
Trial Site Locations
Total: 1 location
1
Ghent University Hospital
Ghent, Belgium, 9000
Actively Recruiting
Research Team
G
Gwendolyn Prof. Dr. Portzky
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
PREVENTION
Number of Arms
1
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