NCT05539534

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
10,000

participants targeted

Target at P75+ for not_applicable

Timeline
30mo left

Started Jan 2019

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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 Progress76%
Jan 2019Dec 2028

Study Start

First participant enrolled

January 7, 2019

Completed
2.9 years until next milestone

First Submitted

Initial submission to the registry

November 29, 2021

Completed
10 months until next milestone

First Posted

Study publicly available on registry

September 14, 2022

Completed
6.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2028

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2028

Last Updated

December 6, 2023

Status Verified

December 1, 2023

Enrollment Period

10 years

First QC Date

November 29, 2021

Last Update Submit

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

EXPERIMENTAL

This is a one-arm trial. The intervention group receives a training on suicide prevention.

Behavioral: 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.

Training

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

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

Study Sites (1)

Ghent University Hospital

Ghent, 9000, Belgium

RECRUITING

MeSH Terms

Conditions

Behavior

Study Officials

  • Gwendolyn Portzky, MD

    University Hospital, Ghent

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Gwendolyn Prof. Dr. Portzky

CONTACT

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

Locations