Study Summary
This trial will compare how well a self-administered vs. clinician-administered protocol helps Veterans experiencing suicidal ideation.
Eligible Conditions
- Attempted Suicide
- Suicidal Thoughts
Treatment Effectiveness
Effectiveness Progress
Study Objectives
1 Primary · 3 Secondary · Reporting Duration: Administered daily for eight consecutive days
Administered daily for eight consecutive days
Change in Crisis Response Plan Use from the previous daily assessment
Change in Patient Health Questionnaire - 2 scores from the previous daily assessment
Change in Positive and Negative Affect Schedule - Short Form scores from the previous daily assessment
Change in Suicide Visual Analog Scale scores from the previous daily assessment
Trial Safety
Safety Progress
Trial Design
2 Treatment Groups
Clinician-administered Crisis Response Plan
1 of 2
Self-administered Crisis Response Plan
1 of 2
Active Control
Experimental Treatment
150 Total Participants · 2 Treatment Groups
Primary Treatment: Crisis Response Planning for Suicide Risk · No Placebo Group · N/A
Self-administered Crisis Response Plan
Behavioral
Experimental Group · 1 Intervention: Crisis Response Planning for Suicide Risk · Intervention Types: BehavioralClinician-administered Crisis Response Plan
Behavioral
ActiveComparator Group · 1 Intervention: Crisis Response Planning for Suicide Risk · Intervention Types: BehavioralTrial Logistics
Trial Timeline
Screening: ~3 weeks
Treatment: Varies
Reporting: administered daily for eight consecutive days
Who is running the clinical trial?
Ohio State UniversityLead Sponsor
712 Previous Clinical Trials
463,764 Total Patients Enrolled
Eligibility Criteria
Age 18+ · All Participants · 3 Total Inclusion Criteria
Mark “Yes” if the following statements are true for you:They had thoughts of death or suicide within the past month.
To be 18 years old or older is to be considered an adult in the eyes of the law
suicides
US military veterans are committing suicide at an alarming rate
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Conditions
Cancer Related
Treatments