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Clinical Trial Summary

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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Adolescent
  • Adult
  • Ambulatory Care
  • Continuity of Patient Care
  • Crisis Intervention
  • Depression
  • Depressive Disorder
  • Emergencies
  • Emergency Service, Hospital
  • Loneliness
  • Mental Disorder
  • Mental Disorders
  • Mental Health
  • Mental Health Services
  • Outpatient Clinics, Hospital
  • Outpatients
  • Patient Care Planning
  • Secondary Prevention
  • Social Support
  • Suicidal Ideation
  • Suicide
  • Suicide Prevention
  • Suicide, Attempted

NCT number NCT04893447
Study type Interventional
Source St. Luke's Health System, Boise, Idaho
Contact
Status Active, not recruiting
Phase N/A
Start date May 20, 2021
Completion date July 16, 2024

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