NCT06629220

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

87
On Track

Trial Health Score

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

Enrollment
13

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jan 2025

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 4, 2024

Completed
4 days until next milestone

First Posted

Study publicly available on registry

October 8, 2024

Completed
3 months until next milestone

Study Start

First participant enrolled

January 10, 2025

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 31, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 31, 2026

Completed
Last Updated

April 14, 2026

Status Verified

April 1, 2026

Enrollment Period

1.2 years

First QC Date

October 4, 2024

Last Update Submit

April 9, 2026

Conditions

Keywords

co-creationparticipatory researchmensuicide preventionsuicidal ideationmale health

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

OTHER

All participants will be invited to participate in the co-creation meetings.

Other: Tools

Interventions

ToolsOTHER

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.

Co-creation meetings

Eligibility Criteria

Age18 Years+
Sexall(Gender-based eligibility)
Gender Eligibility DetailsSelf-identified male participants can participate (based on gender and not sex)
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (1)

Flemish Centre of Expertise in Suicide Prevention, Ghent University

Ghent, 9000, Belgium

Location

Related Publications (3)

  • Boyle, E. (2007),

    BACKGROUND
  • Hanlon 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: 36377305BACKGROUND
  • Watling 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

Suicide PreventionSuicidal IdeationMultiple Endocrine Neoplasia Type 1

Condition Hierarchy (Ancestors)

SuicideSelf-Injurious BehaviorBehavioral SymptomsBehaviorMultiple Endocrine NeoplasiaEndocrine Gland NeoplasmsNeoplasms by SiteNeoplasmsNeoplasms, Multiple PrimaryNeoplastic Syndromes, HereditaryGenetic Diseases, InbornCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesEndocrine System Diseases

Study Officials

  • Gwendolyn Portzky, PhD

    University Ghent

    PRINCIPAL INVESTIGATOR

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

Locations