Focused Suicide Prevention Strategy for Youth Presenting to the Emergency Department With Suicide Related Behaviour
Suicide, Attempted | Suicidal Ideation | Behavioral Symptoms | Suicide and Self-harm | Suicide | Suicide...Suicide is the leading cause of death due to illness among Canadian youth, claiming more lives than any medical illness, including cancer. Suicide prevention is possible, and early intervention is needed. The investigators will examine the effectiveness of a previously-piloted, ED-based suicide prevention intervention, across Canadian sites, using a randomized clinical trial design. The investigators will determine whether the patient- and family-centered intervention is more effective than enhanced usual care in reducing suicide-related behaviors in 330 youth at high-risk of suicide.
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Conditions de participation
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Sexe:
ALL -
Âges admissibles:
12 to 17
Critères de participation
Inclusion Criteria:
* Youth presenting in the Emergency Department with SIQ-Jr score ≥ 31,
* Has a participating parent or caregiver who is able to communicate easily in English, or is willing to communicate using a hospital-organized translator,
* Between the ages 12-17 years old,
* Living in the catchment area of one of the three hospital sites and access to a telephone.
Exclusion Criteria:
* Score of 3 on KSADS screen for current psychosis or elevated mood
* Moderate to severe intellectual disability, and/or autism based on clinical chart.
Lieu de l'étude
McMaster Children's Hospital - Hamilton Health Sciences
McMaster Children's Hospital - Hamilton Health SciencesHamilton, Ontario
Canada
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Alberta Children's Hospital - Alberta Health Services & University of Calgary
Alberta Children's Hospital - Alberta Health Services & University of CalgaryCalgary, Alberta
Canada
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Trillium Health Partners
Trillium Health PartnersMississauga, Ontario
Canada
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The Hospital for Sick Children
The Hospital for Sick ChildrenToronto, Ontario
Canada
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- Étude parrainée par
- The Hospital for Sick Children
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT06225661