Tracking suicide attempts and suicidal thoughts in Flanders
Official title: The Epidemiology of Suicide Attempts and Suicidal Thoughts in Flanders
Run by University Hospital, Ghent · NCT07021404 · Data updated 2026-11-12
This project collects detailed information about people in Flanders who have suicidal thoughts or who have survived suicide attempts to see how often these events happen, which methods are used, and whether they get follow-up care.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 12 Years and up |
| Sex | All |
| Enrollment | 50000 (estimated) |
| Sponsor | University Hospital, Ghent Academic / other |
| Locations | 33 sites (Aalst and 32 other locations) |
| Status | Recruiting |
| Started | December 31, 2006 |
| Main results expected | March 31, 2033 |
| Study ends | March 31, 2033 |
| Registry record updated | June 15, 2025 |
| Trial ID | NCT07021404 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal participants are people who present alive to participating healthcare services in Flanders after a suicide attempt or with current suicidal thoughts.
✕Probably not a fit
People with accidental overdoses or intoxication without suicidal intent, individuals who died before arrival, and those treated outside the participating hospitals or region are not eligible and will not benefit from this project.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational project registers the frequency and characteristics of suicidal ideation and suicide attempts among individuals presenting to emergency departments, psychiatric hospitals, mobile crisis teams, and general practitioners at participating centers in Flanders. Clinical staff conduct a semi-structured interview using the Guideline for Suicide Care and Evaluation (LOES) to record sociodemographic details, mental state, history of self-harm, method of attempt, and immediate care needs. The LOES basic assessment is done shortly after presentation to document cognition, observable behavior, psychiatric concerns, social support, hopelessness, and willingness to engage in follow-up. Data are compiled to map suicidal behaviors regionally and to identify gaps in aftercare and prevention pathways across sites.
Why it matters
Potential benefit: If successful, findings could help improve how emergency and mental health services identify people at risk and provide timely follow-up care in Flanders.
How similar studies have gone: Similar regional surveillance and registry efforts have previously provided valuable information for prevention and care planning, so the approach is established rather than novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Everyone who is admitted alive to the emergency department after a suicide attempt is included. All methods used during the suicide attempt are included. Regarding the method of suicide attempts, a distinction is made between self-injury (hanging, strangulation, drowning, stab and cut wounds, jumping from a height, etc.) and self-poisoning (ingestion of (psycho)pharmaceuticals, drugs, alcohol, chemicals, or other harmful substances). * Everyone who is admitted with suicidal thoughts Exclusion Criteria: * Accidental overdose, e.g., someone taking medication for a medical condition without any intent to harm themselves * Alcohol intoxication without any intent to harm oneself * Accidental overdose involving party drugs * Individuals who were deceased upon arrival at the hospital due to suicide
Where it's running
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Azorg
Aalst, Belgium Recruiting -
Ziekenhuis aan de Stroom (UKJA)
Antwerp, Belgium Recruiting -
Universitair ziekenhuis Antwerpen
Antwerp, Belgium Recruiting -
Psychiatrisch ziekenhuis Bilzen-Hoeselt
Bilzen, Belgium Recruiting -
Imeldaziekenhuis
Bonheiden, Belgium Recruiting -
AZ Klina
Brasschaat, Belgium Recruiting
Show 27 more locations
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AZ sint Jan
Bruges, Belgium Recruiting -
AZ sint Lucas
Bruges, Belgium Recruiting -
AZ Sint Vincentius
Deinze, Belgium Recruiting -
AZ Sint Blasius
Dendermonde, Belgium Recruiting -
AZ Monica
Deurne, Belgium Recruiting -
AZ Diest
Diest, Belgium Recruiting -
AZ Alma
Eeklo, Belgium Recruiting -
Ziekenhuis Geel
Geel, Belgium Recruiting -
Ziekenhuis Oost Limburg
Genk, Belgium Recruiting -
AZ Jan Palfijn
Ghent, Belgium Recruiting -
AZ Sint-Lucas
Ghent, Belgium Recruiting -
AZ Sint Maria
Halle, Belgium Recruiting -
AZ Herentals
Herentals, Belgium Recruiting -
Jan Yperman ziekenhuis
Ieper, Belgium Recruiting -
Sint-Jozefskliniek
Izegem, Belgium Recruiting -
AZ Groeninge
Kortrijk, Belgium Recruiting -
Heilig Hart Lier
Lier, Belgium Recruiting -
AZ Voorkempen
Malle, Belgium Recruiting -
AZ Sint Maarten
Mechelen, Belgium Recruiting -
AZ oostende
Ostend, Belgium Recruiting -
AZ Oudenaarde
Oudenaarde, Belgium Recruiting -
AZ Delta
Roeselare, Belgium Recruiting -
Sint-Trudo ziekenhuis
Sint-Truiden, Belgium Recruiting -
Sint Andriesziekenhuis
Tielt, Belgium Recruiting -
AZ West
Veurne, Belgium Recruiting -
O.L.V. van Lourdes ziekenhuis Waregem
Waregem, Belgium Recruiting -
Vitaz
Sint-Niklaas, Belgium Active not recruiting
Study contacts
- Principal investigator: Gwendolyn Portzky, Prof — University Ghent
- Study coordinator: Nikita Vancayseele, Msc
- Email: nikita.vancayseele@ugent.be
- Phone: +32 (0)9 332 07 75
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Recovery-oriented suicide prevention for young people at clinical high risk for psychosis
This program tests a peer-supported, clinician-led suicide prevention group for young people at clinical high risk for psychosis to see if it helps reduce suicidal thoughts and support recovery.
-
Digital sleep treatment for teens with insomnia after hospitalization
This project will try a six-session digital cognitive behavioral therapy for insomnia (Sleepio) plus usual care to see if it helps 14–18-year-olds recently hospitalized for suicide risk who have insomnia.
-
Shame-focused cognitive behavioral therapy to reduce suicide risk in hospitalized teens
This program will test whether shame-focused cognitive behavioral therapy helps hospitalized teens (ages 13–18) with recent suicide attempts or severe suicidal thoughts reduce shame and lower suicide risk.
-
Crisis Response Planning added to intensive Cognitive Processing Therapy to reduce suicide risk in PTSD
We will test whether adding Crisis Response Planning to intensive Cognitive Processing Therapy helps reduce suicidal thoughts and behaviors in military members and veterans with PTSD.
-
Teen Recovery: Inspiration, Support, and Empowerment program
This pilot will test whether an online peer-led recovery and support program helps 15–18-year-olds recently discharged from psychiatric care reduce suicidal thoughts, depression, anxiety, and re-hospitalization.
-
I-CARE digital program to teach coping skills during psychiatric boarding
This project will test whether the I-CARE digital program helps adolescents (ages 12–17) boarding in the emergency department for suicide risk learn coping skills and feel less distressed.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.