Safety Planning Intervention to Reduce Short Term Risk

Completed · Not applicable

Conditions studied: Suicide, Attempted

In brief

This study will determine the efficacy of Safety Planning Intervention (SPI) compared to receiving risk factors and warning sign information (RWI) in recent suicide attempters during the 6 months following an acute care visit on: (1) suicidal behaviors; (2) mental health/substance use treatment engagement; (3) suicide-related coping strategies; (4) suicidal ideation; and (5) use of means restriction.

Key facts

Study ID

NCT03227991

Run by

New York State Psychiatric Institute

People needed

422

Starts

2017-09-10

Expected to finish

2020-06-30

Last updated by the study team

2024-01-05

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Presented for an acute care visit within 8 weeks of a suicide attempt, interrupted or aborted attempt, or suicidal ideation with intent and plan within 4 weeks.
• Are 18 years of age or older
• Able to speak and read English
• Able to understand the nature of the study, provide written informed consent, and complete study procedures
• Have been evaluated by a health care professional who provides permission for research staff to approach the patient.

You may not qualify if…

• Under 18 years of age
• Cannot speak or read English
• Unable to understand the nature of the study, provide written informed consent, or complete study procedures
• Unable or unwilling to provide a personal phone number for follow up purposes.

Where it is running

• University of Massachusetts — Worcester, Massachusetts, United States
• New York State Psychiatric Institute — New York, New York, United States
• University of Pennsylvania — Philadelphia, Pennsylvania, United States

Full record on ClinicalTrials.gov

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