Effectiveness of the Suicidal Crisis Intervention (SCI)

Recruiting N/A Interventional Study
Suicide Suicidal Ideation Suicide, Attempted
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Treatment
Participants needed
390 (estimated)
Sponsor
University Hospital, Ghent · Other
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About This Trial

The main objective of this project is to be able to offer a new, specific evidence-based short-term treatment method, the Suicidal Crisis Intervention (SCI), to reduce suicidality. In addition, this study aims to investigate the influence of SCI on other important aspects of suicidality (secondary goal) such as hopelessness, defeat, entrapment, and interpersonal needs.

Trial Locations
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Eligibility Criteria
Inclusion Criteria Patient: * After a suicide attempt or suicidal crisis * ≥ 18 years * Availability of a smartphone, tablet and/or computer with internet access, * Dutch-speaking. Exclusion Criteria Patient: * Limited comprehension, cognitive impairment * Psychotic disorder * Unsuitable for indi…
Contacts

Eva De Jaegere, Msc

+32 (0)9 332.07.75

eva.dejaegere@ugent.be

CONTACT

Pauline Stas, Msc

+32 (0)9 332.07.75

pauline.stas@ugent.be

CONTACT