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Behavioral Intervention
Safety Planning Intervention with Navigation Services for Suicide
N/A
Waitlist Available
Led By Aaron Blashill, Ph.D.
Research Sponsored by San Diego State University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
1) age 15 to 29 years; 2) identifies as gay, lesbian, bisexual, transgender, genderqueer, asexual, pansexual, non-binary, or another non-exclusively heterosexual identity, and/or reports same-gender romantic attraction, and/or reports same-gender sexual behavior in the past 12 months; 3) resides in San Diego County, California; 4) speaks English; 5) is willing and able to provide informed consent; 6) reports suicidal ideation over the past two weeks, as indicated by the clinician-administered Columbia-Suicide Severity Rating Scale (C-SSRS) Baseline version; and 7) reports a lifetime history of one or more suicide attempts.
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up change from baseline suicide-related external coping scores at 3 and 6 months
Awards & highlights
Summary
This trial aims to test a support program for young people from sexual and gender minority groups who are at high risk of suicide. The program combines safety planning with ongoing guidance to help participants feel more connected and teach them how to cope with suicidal thoughts. Attachment-based family therapy (ABFT) has been adapted to address the needs of transgender and gender diverse youth experiencing suicidal thoughts and behavior.
Eligible Conditions
- Suicide
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ change from baseline thwarted belongingness scores at 3 and 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change from baseline thwarted belongingness scores at 3 and 6 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Suicide-Related Coping Scale (SRCS) - External Coping Skills
Suicide-Related Coping Scale (SRCS) - Internal Coping Skills
The Interpersonal Needs Questionnaire-15 (INQ-15) - Thwarted Belongingness
Trial Design
1Treatment groups
Experimental Treatment
Group I: Safety Planning Intervention with Navigation ServicesExperimental Treatment1 Intervention
A patient navigation (PN) intervention for SGM youth/emerging adults designed to target mechanisms (i.e., decreasing thwarted belongingness and increasing suicide-related coping skills) that theoretically underlie suicide. The proposed intervention will integrate a single-session, empirically supported, suicide prevention intervention (Safety Planning Intervention; SPI) with PN services (PN+SPI). The patient navigator will deliver the SPI and continue frequent contact for the purpose of providing motivational enhancement, problem-solving, reinforcing coping strategies, and connecting participants to social support and mental health resources (e.g., SGM-specific support groups within the community).
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Safety Planning Intervention with Navigation Services
2021
N/A
~40
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Who is running the clinical trial?
San Diego State UniversityLead Sponsor
163 Previous Clinical Trials
113,391 Total Patients Enrolled
2 Trials studying Suicide
179 Patients Enrolled for Suicide
National Institute of Mental Health (NIMH)NIH
2,869 Previous Clinical Trials
2,777,505 Total Patients Enrolled
123 Trials studying Suicide
1,237,699 Patients Enrolled for Suicide
Aaron Blashill, Ph.D.Principal InvestigatorSan Diego State University
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