Effect of Suicide Prevention Training for Professionals
1 other identifier
interventional
10,000
1 country
1
Brief Summary
Annually a substantial number of courses and trainings are organised in Flanders with regard to suicide prevention.These trainings are mainly aimed at intermediaries, such as caregivers, teachers, police, etc. From previous research it appears that such trainings are one of the most effective strategies for increasing knowledge, attitudes, skills and self-confidence with regard to dealing with persons who are suicidal and with crisis situations. However, such research has not yet been conducted in Flanders, which means that the effect of the training on the knowledge and attitudes of the intermediaries could not yet be determined. Therefore, this study aims to determine the effect of the trainings in Flanders. These trainings are organised by the Centre for the Prevention of Suicide (CPZ) and by the suicide prevention workers of the Centers for Mental Health Care. All participants who register for one of these trainings will be invited by e-mail at three moments to complete an online questionnaire:
- Pre-test: one week before the training,
- Post-test: after the training,
- Follow-up: three months after training.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Jan 2019
Longer than P75 for not_applicable
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
January 7, 2019
CompletedFirst Submitted
Initial submission to the registry
November 29, 2021
CompletedFirst Posted
Study publicly available on registry
September 14, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2028
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 31, 2028
December 6, 2023
December 1, 2023
10 years
November 29, 2021
December 5, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
Degree of knowledge and attitudes on suicide and suicide prevention
Self-developed questionnaire about knowledge and attitudes on suicide and suicide prevention based on the Attitudes about Suicide Scale (ATTS).
Change in knowledge and attitudes at baseline (i.e., from one week before the start of the training) compared to post-test (immediately after the training, i.e. up to 3 days) and follow-up (3 months after post-test)
Secondary Outcomes (1)
Rate of responses to suicide
Change in Response to suicide at baseline (i.e., from one week before the start of the training) compared to post-test (immediately after the training, i.e. up to 3 days) and follow-up (3 months after post-test)
Other Outcomes (2)
Socio-demographic characteristics
Baseline (i.e., from one week before the start of the training)
Evaluation of the training
Post-test (immediately after the training, i.e. up to 3 days)
Study Arms (1)
Training
EXPERIMENTALThis is a one-arm trial. The intervention group receives a training on suicide prevention.
Interventions
Suicide prevention training in Flanders is organised by the Centre for the Prevention of Suicide and the suicide prevention workers of the Centra for Mental Health Care. These trainings are announced via the website zelfmoord1813.be/vormingen or are organized on demand. When a participant registers, they will be invited to participate in the study one week before the training.
Eligibility Criteria
You may qualify if:
- Participating in a suicide prevention training organised by 'Centrum ter Preventie van Zelfdoding' or 'Suïcidepreventiewerking Centra Geestelijke Gezondheidszorg'
You may not qualify if:
- Not participating in a suicide prevention training organised by 'Centrum ter Preventie van Zelfdoding' or 'Suïcidepreventiewerking Centra Geestelijke Gezondheidszorg'
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University Ghentlead
Study Sites (1)
Ghent University Hospital
Ghent, 9000, Belgium
MeSH Terms
Conditions
Study Officials
- PRINCIPAL INVESTIGATOR
Gwendolyn Portzky, MD
University Hospital, Ghent
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 29, 2021
First Posted
September 14, 2022
Study Start
January 7, 2019
Primary Completion (Estimated)
December 31, 2028
Study Completion (Estimated)
December 31, 2028
Last Updated
December 6, 2023
Record last verified: 2023-12