Crucial elements in suicide prevention strategies.
Merete Nordentoft
https://pubmed.ncbi.nlm.nih.gov/21130823/Actively Recruiting
Led by University Hospital, Ghent · Updated on 2025-11-18
390
Participants Needed
12
Research Sites
34 weeks
Total Duration
Researchers are evaluating the Suicidal Crisis Intervention SCI as a new short-term treatment method for people after a suicidal crisis or suicide attempt. This study aims to determine if SCI can reduce suicidality and also explore its effect on related factors such as hopelessness, defeat, entrapment, and interpersonal needs. The SCI was developed to provide evidence-based care in Flanders, addressing the limited interventions currently available for this high-risk group. The study compares two groups one receiving the SCI alongside their usual treatment, and the other receiving only their usual treatment. The SCI includes four sessions focusing on providing insight into suicidal crises, involving loved ones, creating a safety plan, and ensuring continuity of care. It emphasizes a structured, person-centered approach and aims to motivate participants toward specialized care. Participants will be followed for approximately 222 days after randomization. Researchers will assess changes in suicidality using the Beck Scale for Suicide Ideation at multiple points, along with secondary measures such as suicidal behavior, hopelessness, defeat, entrapment, isolation, follow-up care readiness, and treatment satisfaction. Assessments are conducted at baseline, 42 days, 132 days, and 222 days to monitor progress and outcomes throughout the study period.
CONDITIONS
Effectiveness of the Suicidal Crisis Intervention (SCI)
E
Eva De Jaegere, Msc
P
Pauline Stas, Msc
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University Hospital, Ghent
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Approximately 6 weeks (42 days)
Participants receive the Suicidal Crisis Intervention (SCI), a short-term treatment consisting of 4 sessions that aims to provide tools for dealing with future suicidal crises, involving close relatives and focusing on continuity of care. Participants in the control group receive their usual treatment.
4 treatment sessions over the course of the intervention
Duration - Approximately 6 months (180 days)
Participants are followed after treatment to assess changes in suicidality, hopelessness, suicidal behavior, and other related outcomes, as well as treatment satisfaction.
2 follow-up visits at 132 days and 222 days after randomization
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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Merete Nordentoft
https://pubmed.ncbi.nlm.nih.gov/21130823/Keith Hawton, Daniel Zahl, Rosamund Weatherall
https://pubmed.ncbi.nlm.nih.gov/12777346/E C Harris, B Barraclough
https://pubmed.ncbi.nlm.nih.gov/9229027/University Hospital, Ghent
Lead Sponsor