Evaluation of a Training for Healthcare Providers in Supporting Men Experiencing Suicidal Ideation
1 other identifier
interventional
119
1 country
1
Brief Summary
The primary objective of this study is to assess how healthcare providers perceive and evaluate the developed e-learning. The findings will inform potential adjustments to enhance the e-learning as needed.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started May 2025
Shorter than P25 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
First Submitted
Initial submission to the registry
January 22, 2025
CompletedFirst Posted
Study publicly available on registry
February 5, 2025
CompletedStudy Start
First participant enrolled
May 27, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 13, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
July 13, 2025
CompletedApril 13, 2026
April 1, 2026
2 months
January 22, 2025
April 9, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
Competencies related to working with male clients (self-efficacy)
Adaptation of the Engaging Men in Therapy Scale (EMITS): scale of 13 items to be rated on a scale from 1 (strongly disagree) to 5 (strongly agree), resulting in a total score of 13-65. Higher scores indicating higher self-reported competency for engaging with male clients. The adapted version consists of 8 items, as not all aspects of the original questionnaire are included in the evaluated e-learning.
Change from Baseline (before e-learning) to post-test (immediatly after e-learning of 30-60 minutes); assessed up to 3 days after pre-test
Evaluation of the training
self-developed questionnaire: score on a scale of 1 (not good at all) to 10 (Excellent); 10 evaluation statements to be rated on a scale of 1 (totally disagree) to 5 (totally agree); 9 open questions; one question about the length of the e-learning (too short, too long or just fine)
Post-test (immediatly after e-learning of 30-60 minutes), up to 3 days after pre-test
Secondary Outcomes (1)
self-efficacy
Change from Baseline (before e-learning) to post-test (immediatly after e-learning of 30-60 minutes); assessed up to 3 days after pre-test
Other Outcomes (3)
Socio-demographic variables
Baseline
Work situation
Baseline
Experience with men with suicidal thoughts
Baseline
Study Arms (1)
Gatekeeper training (e-learning)
EXPERIMENTALParticipants in this group (all participants) are asked to complete a questionnaire and then receive access to the online training (e-learning), after which they were asked to complete another questionnaire. In case a participant does not complete the post-test, a reminder will be sent via e-mail three days later.
Interventions
This training supplements existing modules for healthcare providers working with individuals experiencing suicidal thoughts (https://sp-reflex.zelfmoord1813.be/e-learning). Specific information on working with men will be added: * Information on suicidality among men and the importance of gender-sensitive care. * Guidance on recognizing signs of suicidality in men and understanding gender differences in suicide-related communication. * Insights into the impact of gender norms and socialization on suicidality and help-seeking behavior in men experiencing suicidal thoughts. * Awareness of providers' own gender biases and the influence of societal gender norms in treating men with suicidal ideation. * Recommendations for engaging men in treatment, with specific guidance on language and approaches for interacting with men who have suicidal thoughts. Additionally, the e-learning will a model psychoeducation about the role of norms for men experiencing suicidal ideation.
Eligibility Criteria
You may qualify if:
- Healthcare providers (e.g. GP's, psychiatrists, medical doctors, psychologists, psychotherapists, and nurses working in healthcare)
- ≥18y/o
- Access to a smartphone, tablet, or computer with internet connection and proficiency in Dutch
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University Ghentlead
Study Sites (1)
Flemish Centre of Expertise in Suicide Prevention, Ghent University
Ghent, 9000, Belgium
Related Publications (1)
Seidler ZE, Wilson MJ, Benakovic R, Mackinnon A, Oliffe JL, Ogrodniczuk JS, Kealy D, Owen J, Pirkis J, Mihalopoulos C, Le LK, Rice SM. A randomized wait-list controlled trial of Men in Mind: Enhancing mental health practitioners' self-rated clinical competencies to work with men. Am Psychol. 2024 Apr;79(3):423-436. doi: 10.1037/amp0001242. Epub 2023 Nov 27.
PMID: 38010768BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Gwendolyn Portzky, PhD
University Ghent
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
January 22, 2025
First Posted
February 5, 2025
Study Start
May 27, 2025
Primary Completion
July 13, 2025
Study Completion
July 13, 2025
Last Updated
April 13, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share