Randomized controlled trial to determine the best brief suicide prevention intervention for adults and adolescents who screen positive for suicidal ideation or behavior in emergency departments or primary care clinics.
Aim 1: Compare the effectiveness of two brief suicide prevention interventions (safety planning intervention plus structured phone-based follow-up from a suicide prevention hotline (SPI+), versus safety planning intervention plus caring contacts (CC)) to (a) reduce suicidal ideation and behavior, (b) reduce loneliness, (c) reduce return to care for suicidality, and (d) increase uptake of outpatient mental healthcare services over 12 months among adult and adolescent patients screening positive for suicide in emergency departments (EDs) and primary care clinics.
Aim 2: Assess the acceptability of connection and support planning and the safety planning intervention, with or without follow-up among providers and clinical staff in EDs and primary care clinics.
Aim 3: Assess the acceptability of SPI+ and SP+CC among adult and adolescent patients.
Condition | Endogenous depression, Depression (Major/Severe), Suicidal Ideation, Depressed, Crisis Intervention, Psychosis, Depression (Treatment-Resistant), mental disorder, Adolescence, Psychological Disorders, Adult, psychological disorder, psychiatric diseases, psychotic disorders, mental health, Depression (Adult and Geriatric), Mood Disorders (Pediatric), Emergency Room, Suicide, Nursing Care Plans, depressive disorders, mental disease, Loneliness, psychiatric illness, Depression, depressive disorder, Hospital Outpatient Clinic, Social support, Affective Disorders, miserable, mood disorder, Depression (Adolescent), Mood Disorders, psychiatric disorder, mental disorders, psychiatric disease, Mental Health Services, Depression (Pediatric), Suicide attempt, Outpatient, psychiatric disorders, Continuity of Care, psychotic, Ambulatory Care, psychotic disorder, Secondary Prevention, Mental illness, depressed mood |
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Treatment | SPI+, SP+CC (Caring Contacts) |
Clinical Study Identifier | NCT04893447 |
Sponsor | St. Luke's Health System, Boise, Idaho |
Last Modified on | 3 October 2021 |
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