Actively Recruiting

Phase Not Applicable
All Genders
Healthy Volunteers
ID05539534

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

All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Participating in a suicide prevention training organised by 'Centrum ter Preventie van Zelfdoding' or 'Su�fcicidepreventiewerking Centra Geestelijke Gezondheidszorg'
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 screening and enrollment visit (in-person or online)

Outpatient Treatment

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

Follow-up

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

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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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