Co-creation of Tools for Men With Suicidal Thoughts and/or Behavior
1 other identifier
interventional
13
1 country
1
Brief Summary
The primary objective of this project is to co-create suicide prevention tools for men with suicidal thoughts ensuring these tools are supported by their future users. The researchers will organize up to 10 online or live co-creation meetings of maximum 2 hours each in which men (18 years or older) with a history of suicidal thoughts and/or behavior will help develop tools by providing their needs and feedback. Up to 30 men can participate.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jan 2025
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
October 4, 2024
CompletedFirst Posted
Study publicly available on registry
October 8, 2024
CompletedStudy Start
First participant enrolled
January 10, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 31, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 31, 2026
CompletedApril 14, 2026
April 1, 2026
1.2 years
October 4, 2024
April 9, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Co-creation questions
During the meetings, participants will be asked to provide feedback on developed tools and drafts (open questions). Here are some topics and questions the researchers will consider during the meetings: 1. Current healthcare/tools usage 2. Preferences and needs (this will be mainly based on the results of our previous study, BUN B6702024000090) 3. Accessibility and usability of the tool 4. Privacy and confidentiality 5. Social support and sensitivity 6. Help and professional support 7. Continuity and long-term implementation 8. Feedback on prototypes of the tool 9. Feedback on final version of the tool
From enrolment to end of co-creation sessions (10 sessions of 2 hours max over the course of the study)
Other Outcomes (9)
Socio-demographic characteristics: gender
Baseline. Completing the entire 'socio-demographic characteristics questionnaire' will take about 5 minutes
Socio-demographic characteristics: age
Baseline. Completing the entire 'socio-demographic characteristics questionnaire' will take about 5 minutes
Socio-demographic characteristics: history of suicidal ideation
Baseline. Completing the entire 'socio-demographic characteristics questionnaire' will take about 5 minutes
- +6 more other outcomes
Study Arms (1)
Co-creation meetings
OTHERAll participants will be invited to participate in the co-creation meetings.
Interventions
In the co-creation meetings, developed tools will be presented. Participants will be asked to provide feedback and input to tailor these tools to the needs and preferences of men with suicidal thoughts/behavior.
Eligibility Criteria
You may qualify if:
- Men (≥ 18y/o)
- Experienced suicidal thoughts in the past three year
You may not qualify if:
- Limited comprehension
- Acute suicidality (as evaluated by a clinical psychologist of the research team)
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 (3)
Boyle, E. (2007),
BACKGROUNDHanlon CA, McIlroy D, Poole H, Chopra J, Saini P. Evaluating the role and effectiveness of co-produced community-based mental health interventions that aim to reduce suicide among adults: A systematic review. Health Expect. 2023 Feb;26(1):64-86. doi: 10.1111/hex.13661. Epub 2022 Nov 14.
PMID: 36377305BACKGROUNDWatling D, Preece M, Hawgood J, Bloomfield S, Kolves K. Developing an Intervention for Suicide Prevention: A Rapid Review of Lived Experience Involvement. Arch Suicide Res. 2022 Apr-Jun;26(2):465-480. doi: 10.1080/13811118.2020.1833799. Epub 2020 Oct 18.
PMID: 33073734BACKGROUND
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
October 4, 2024
First Posted
October 8, 2024
Study Start
January 10, 2025
Primary Completion
March 31, 2026
Study Completion
March 31, 2026
Last Updated
April 14, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share