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Advancing Suicide Intervention Strategies for Teens (ASSIST): study protocol for a multisite randomised controlled trial.
Adrian, Molly; McCauley, Elizabeth; Gallop, Robert; Stevens, Jack; Jobes, David A; Crumlish, Jennifer; Stanley, Barbara; Brown, Gregory K; Green, Kelly L; Hughes, Jennifer L; Bridge, Jeffrey A.
Afiliação
  • Adrian M; University of Washington, Seattle, Washington, USA adriam@uw.edu.
  • McCauley E; University of Washington, Seattle, Washington, USA.
  • Gallop R; West Chester University, West Chester, Pennsylvania, USA.
  • Stevens J; Ohio State University, Columbus, Ohio, USA.
  • Jobes DA; The Catholic University of America, School of Arts and Sciences, Washington, DC, USA.
  • Crumlish J; The Catholic University of America, School of Arts and Sciences, Washington, DC, USA.
  • Stanley B; Columbia University Medical Center, New York, New York, USA.
  • Brown GK; University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Green KL; University of Pennsylvania, Philadelphia, Pennsylvania, USA.
  • Hughes JL; Nationwide Children's Hospital, Columbus, Ohio, USA.
  • Bridge JA; The Ohio State University College of Medicine, Research Institute at Nationwide Children's Hospital, Columbus, Ohio, USA.
BMJ Open ; 13(12): e074116, 2023 12 12.
Article em En | MEDLINE | ID: mdl-38086585
ABSTRACT

INTRODUCTION:

Brief interventions that reduce suicide risk following youth's experience with acute care due to suicidality are needed. METHODS AND

ANALYSIS:

The study will use a three-arm randomised controlled trial designed to test the effectiveness of the Safety Planning Intervention with structured follow-up (SPI+) and the Collaborative Assessment and Management of Suicidality (CAMS) compared with enhanced usual care. The primary outcomes measure will be suicidal events, defined as death by suicide, attempted suicide, preparatory acts toward imminent suicidal behaviour or suicidal ideation resulting in a change in emergency evaluation or inpatient admission. Secondary measures will be the number of suicide attempts and severity of suicidal ideation. The experimental interventions, SPI+ and CAMS, consist of up to eight sessions over approximately 8 weeks that are designed to manage (SPI+) or treat (CAMS) patient-identified 'drivers' of suicidal thoughts and behaviours. Mechanisms and moderators of change will be evaluated to understand treatment impacts. ETHICS AND DISSEMINATION This study has been approved by the Seattle Children's Institutional Review Board and is monitored by external agencies including the University of Washington Institute for Translational Health Sciences, and a National Institute of Mental Health (NIMH)-appointed Data Safety and Monitoring Board. Trial results will help establish evidence towards safe and effective treatment strategies for youth transitioning from acute to outpatient care due to a suicidal crisis. The data will be shared with the NIMH Data Archives and disseminated through publications and conferences. TRIAL REGISTRATION NUMBER NCT05078970.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tentativa de Suicídio / Ideação Suicida Limite: Adolescent / Child / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Tentativa de Suicídio / Ideação Suicida Limite: Adolescent / Child / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article