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

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07259408
Enrollment
40
Registered
2025-12-02
Start date
2025-10-27
Completion date
2026-05-01
Last updated
2025-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Suicidal Ideation, Suicide, Suicide Prevention

Keywords

Safety Plan, Safety Planning, Suicide prevention, Risicoformulering, risk formulation, detention, prison, incarceration

Brief summary

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

OTHERCo-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 on usability, perceived barriers, and suggestions for real-world implementation in the detention context. Interviews are repeated up to three times per professional participants depending on availability and co-creation progress. For individuals in detention there is only one interview. Feedback from all participants will be used to adapt and refine the tools for future use in detention facilities.

Sponsors

University Ghent
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion 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

Design outcomes

Primary

MeasureTime frameDescription
Evaluation of Suicide Prevention Tools in the Detention ContextEach participant is assessed during one (for incarcerated individuals) or up to three (for professionals) interviewsThis outcome measure assesses the usability, applicability, and improvement potential of three suicide prevention tools based on qualitative feedback from professionals working in detention and individuals in detention. Through semi-structured interviews, the study explores how these tools are experienced in practice, identifies perceived strengths and limitations, and gathers concrete suggestions for adaptation to better fit the detention environment.

Countries

Belgium

Contacts

Primary ContactEva De Jaegere, PhD
eva.dejaegere@ugent.be+32 (0)9 332.07.75
Backup ContactKirsten Pauwels, Msc
kirsten.pauwels@ugent.be+32 (0)9 332.07.75

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026