Effect of Suicide Prevention Training for Professionals

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorUniversity Ghent

About this trial

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.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Participating in a suicide prevention training organised by 'Centrum ter Preventie van Zelfdoding' or 'Suïcidepreventiewerking Centra Geestelijke Gezondheidszorg'

Disqualifiers

Not participating in a suicide prevention training organised by 'Centrum ter Preventie van Zelfdoding' or 'Suïcidepreventiewerking Centra Geestelijke Gezondheidszorg'

Trial design

Design model

Single group

Treatments tested in this trial

  • Training on suicide prevention

    Behavioral

    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.

Treatment groups

10,000 Participants
are divided into 1 treatment group
Group A: TrainingExperimental treatment 1 intervention

Trial outcomes

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).

Time frame
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

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.

Time frame
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

1

Socio-demographic characteristics

Socio-demographic characteristics such as gender, age, and work.

Time frame
Baseline (i.e., from one week before the start of the training)
2

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.

Time frame
Post-test (immediately after the training, i.e. up to 3 days)

Sponsors and contacts

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