Suicide Prevention Among Recipients of Care (SPARC)
Suicide, Suicide, Attempted, Suicidal Ideation
About this trial
This is an interventional prevention trial for Suicide focused on measuring Brief Interventions, Caring Contacts, Care Transitions, Follow-up, Emergency Department, Primary Care, Safety Planning Intervention, Safety Plan, Suicide, Suicide Prevention, Adult, Adolescent, Brief Contact Intervention
Eligibility Criteria
Inclusion Criteria:
- Patient at St. Luke's Health System Emergency Department or Primary Care Clinic
- 12-17 years old (adolescents) or 18+ years old (adults)
- Screened positive for suicide risk on C-SSRS (any response of "yes") during current visit, or current visit is related to a suicide attempt
- Access to a phone for the duration of the study with the ability to receive calls
- The ability to send and receive email messages (required) and text messages (optional)
- English or Spanish speaking and reading
Exclusion Criteria:
- Unable or unwilling to provide informed consent to participate
- Inappropriate for study participation based on the clinical judgment of provider
Sites / Locations
- St. Luke's Health System
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
SPI+: Safety Planning Intervention plus structured phone-based follow-up
Caring Contacts: Safety Planning Intervention plus Caring Contacts (SP+CC)
The Safety Planning Intervention (SPI+) includes safety planning (moderate or high risk for suicide) or connection & support planning (low risk for suicide) at the clinic or ED, plus a structured telephone-based intervention from a suicide prevention hotline
SP+CC will include safety planning (moderate or high risk for suicide) or connection & support planning (low risk for suicide) at the clinic or ED, plus caring text messages or emails from a suicide prevention hotline.