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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05539534
Other study ID # 2018/1329
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 7, 2019
Est. completion date December 31, 2028

Study information

Verified date December 2023
Source University Ghent
Contact Gwendolyn Prof. Dr. Portzky
Phone +3293320775
Email info@vlesp.be
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 10000
Est. completion date December 31, 2028
Est. primary completion date December 31, 2028
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Participating in a suicide prevention training organised by 'Centrum ter Preventie van Zelfdoding' or 'Suïcidepreventiewerking Centra Geestelijke Gezondheidszorg' Exclusion Criteria: - Not participating in a suicide prevention training organised by 'Centrum ter Preventie van Zelfdoding' or 'Suïcidepreventiewerking Centra Geestelijke Gezondheidszorg'

Study Design


Intervention

Behavioral:
Training on suicide prevention
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.

Locations

Country Name City State
Belgium Ghent University Hospital Ghent

Sponsors (1)

Lead Sponsor Collaborator
University Ghent

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Other Socio-demographic characteristics Socio-demographic characteristics such as gender, age, and work. Baseline (i.e., from one week before the start of the training)
Other Evaluation of the training Self-developed questionnaire about how the participants experienced the training, i.e. how satisfied they were, how applicable the training was, and an overall score of the training. Post-test (immediately after the training, i.e. up to 3 days)
Primary 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 Rate of responses to suicide ONLY APPLICABLE FOR TRAININGS THAT LAST MORE THAN 3 HOURS. Questionnaire Responses to Suicide is a Dutch questionnaire (original name: Vragenlijst Reacties op Suïcidaliteit (VROS). This questionnaire assesses how appropriately someone can react to suicide. The lower the score, the better the person knows how to react. 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)
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