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Recruiting NCT07259408

Co-creation of Tools for People in Detention With Suicidal Thoughts and/or Behavior

Observational Suicide Prevention Suicide Suicidal Ideation

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Co-creation process for suicide prevention tools in detention.
Who it may be relevant to
Registry conditions: Suicide Prevention, Suicide, Suicidal Ideation. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Belgium
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

People in detention are at significantly higher risk of suicide compared to the general population. In Belgian prisons, the suicide rate is five times higher than average. Despite the availability of suicide prevention tools, many are not scientifically validated or adapted to the detention context, leading to inconsistent use and missed warning signs. This study aims to evaluate and adapt three evidence-based suicide prevention tools-the Safety Plan, the guideline for the care and evaluation of suicidality , and the Risk Formulation template-for use in detention settings. Through interviews with both professionals working in prisons and individuals in detention, the study explores how these tools can be made more relevant, practical, and effective in this unique environment. The research involves 40 participants: 20 professionals and 20 individuals in detention. Interviews will gather feedback on the tools' usability, clarity, and fit with the realities of prison life. The ultimate goal is to improve suicide prevention practices in detention by offering tailored, scientifically grounded tools that support both staff and detainees.

Interventions

  • Other Co-creation process for suicide prevention tools in detention
    The intervention consists of a co-creation process involving detained individuals and detention professionals through semi-structured interviews. For professionals, the interviews will focus on the usability, applicability, and implementation of three suicide prevention tools. Interviews with individuals in detention will focus only on the Safety Plan. They will be asked about what helps them in moments of crisis and their views on the Safety Plan in detention. The goal is to collect feedback

Primary outcome measures

  • Evaluation of Suicide Prevention Tools in the Detention Context [Time frame: Each participant is assessed during one (for incarcerated individuals) or up to three (for professionals) interviews]

Eligibility criteria

For professionals working in detention:

Inclusion criteria

  • Aged 18 years or older
  • Currently working in a professional care role within a prison setting (e.g., psychologist, psychiatirst, social worker, nurse, etc.)
  • Experience in supporting or treating incarcerated individuals with suicidal thoughts or behaviours

Exclusion criteria

  • Under the age of 18
  • Not employed in a professional caregiving role within detention (e.g., correctional officers or security staff)

For people in detention:

Inclusion criteria

  • Aged 18 years or older
  • Experienced suicidal thoughts within the past three years

Exclusion criteria

  • Under the age of 18
  • Significant cognitive limitations that would make the participation in an interview infeasible
  • Insufficient command of the Dutch language to understand and respond to interview questions

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Other

Study locations

Belgium · 1 center
  • Flemish Centre of Expertise in Suicide Prevention, Ghent University — Ghent

Identifiers

NCT: NCT07259408 · ONZ-2025-0349

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗