Refinement of Suicide Risk Management Intervention

Not Applicable

Active, not recruiting

• Conditions: Safety Plan; Structured Interview; Narrative Assessment; Crisis Response Plan

• Registration Number: NCT04888845
• Lead Sponsor: University of Utah

Brief Summary

Participants will be randomly assigned to 1 of the 4 interventions using a sequential stratified randomization procedure. We will use sex (M, F) and history of suicide attempts (never, 1, and multiple) as our randomization strata. Participants will be assessed before and after the intervention to study the potential effects of each approach on suicide-related clinical outcomes.

Detailed Description

Not available

Study Timeline

• Study Start: 2021-04-22
• Study First Submitted: 2021-04-29
• Study First Submitted QC: 2021-05-11
• Study First Posted: 2021-05-17
• Status Verified: 2024-12
• Last Update Submitted: 2024-12-05
• Last Update Posted: 2024-12-11
• Primary Completion: 2026-07-30
• Study Completion: 2026-07-30

Recruitment & Eligibility

• Status: ACTIVE_NOT_RECRUITING
• Sex: All
• Target Recruitment: 120

Inclusion Criteria

• Clinical diagnosis of suicide Ideation
• History of suicide attempts

Exclusion Criteria

• Geographic location outside the U.S.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: FACTORIAL

Primary Outcome Measures

Name	Time	Method
Change in suicide relevant thoughts and behaviors after the intervention (Self Injurious Thoughts and Behaviors questionnaire)	During an average of 2-weeks pre-intervention, 2-weeks post-intervention, 1 month follow-up after intervention	Items from the Self Injurious Thoughts and Behaviors questionnaire (Fox et al., 2020) will be used to assess suicide relevant thoughts and behaviors

Trial Locations

Locations (2)

The Ohio State; 🇺🇸 Columbus, Ohio, United States

University of Utah; 🇺🇸 Salt Lake City, Utah, United States