New Generation Therapies for Suicide: Refining Brief Cognitive Behavioral Therapy
Official title: STRENGTHENS: Study To Refine the Effectiveness of New Generation Therapies for Suicide
Run by Ohio State University · NCT07818889 · Data updated 2026-11-12
This study tests different sequences and doses of Brief Cognitive Behavioral Therapy to see if it better reduces suicide risk in adults with recent suicidal thoughts or behavior.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 50 (estimated) |
| Sponsor | Ohio State University Academic / other |
| Locations | 1 site (Columbus, Ohio) |
| Status | Recruiting |
| Started | April 29, 2026 |
| Main results expected | December 31, 2029 |
| Study ends | December 31, 2029 |
| Registry record updated | September 14, 2026 |
| Trial ID | NCT07818889 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults 18 or older with recent suicide risk or behavior, able to understand English and consent, and eligible for outpatient therapy.
✕Probably not a fit
Individuals with conditions that preclude informed consent or engagement in outpatient therapy may not benefit from this intervention.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
Researchers at Ohio State University will use a SMART design to optimize Brief Cognitive Behavioral Therapy (BCBT) for suicide prevention. All participants begin with 4 BCBT sessions and weekly assessments, plus 4 weeks of ecological momentary assessment and digital phenotyping to track fluctuations in suicidality. The trial aims to identify which sequences and doses of BCBT components most effectively lower suicide risk. The study is funded by The Jordan Elizabeth Harris Foundation and involves outpatient treatment at the Columbus, Ohio site. This design allows adjustments based on each participant's response to initial therapy.
Why it matters
Potential benefit: If successful, the study could identify more effective ways to deliver BCBT to reduce suicidal thoughts and behaviors.
How similar studies have gone: Prior work in sequential randomized designs has helped tailor psychotherapy components, but the exact SMART approach for BCBT in suicidality is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 18 years of age or older; suicidal ideation (assessed with the SSI) and/or suicidal behavior within the past month (assessed with the SITBI-R), psychiatric hospitalization for elevated suicide risk within the past month, and/or SCS-R total score \>21; eligibility to understand and speak the English language; ability to complete the informed consent process Exclusion Criteria: * impaired mental status that precludes the ability to provide informed consent (e.g., intoxication, psychosis, mania) and/or a medical or psychiatric condition that precludes the ability to engage in outpatient therapy
Where it's running
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Department of Psychiatry and Behavioral Health
Columbus, Ohio, United States Recruiting
Study contacts
- Principal investigator: Melanie Bozzay, PhD — Ohio State University
- Study coordinator: Anna Crouser, MSW, LSW
- Email: anna.crouser@osumc.edu
- Phone: 614-293-2554
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.