Youth suicide risk factors and personalized reduction strategies in young adults
Official title: Youth Suicide Risk Factors: Clinical, Neuroimaging, Genetic, and Microbiome Insights, and Predictors of Response to Deep Transcranial Magnetic Stimulation (dTMS)
Run by Fondazione Policlinico Universitario Agostino Gemelli IRCCS · NCT07188506 · Data updated 2026-11-12
This study tests whether combining clinical data, genetic information, neuroimaging, and microbiome data can help identify risk factors and see if a dTMS-based intervention reduces suicide risk in young adults with mood disorders.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 25 Years |
| Sex | All |
| Enrollment | 180 (estimated) |
| Sponsor | Fondazione Policlinico Universitario Agostino Gemelli IRCCS Academic / other |
| Locations | 1 site (Roma, RM) |
| Status | Recruiting |
| Started | November 15, 2025 |
| Main results expected | December 31, 2027 |
| Study ends | October 31, 2028 |
| Registry record updated | August 28, 2026 |
| Trial ID | NCT07188506 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal participants are 18–25 years old with a mood disorder (depression or bipolar) who can undergo MRI and speak Italian.
✕Probably not a fit
Individuals with severe neurological conditions, cognitive impairment, inability to consent, or non-Italian speakers may not benefit from the study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
YOU-SURF aims to integrate multimodal data to identify risk factors for suicide in youth and test a dTMS-based intervention. The study includes clinical assessments, blood tests, genome-wide genotyping, and neuroimaging, alongside an innovative neuromodulation treatment. It compares participants with mood disorders aged 18–25 to a control group without DSM-5 disorders, all undergoing MRI and Italian-language screening. The approach targets personalized risk profiling and tailored treatment strategies based on multiple biological and clinical dimensions.
Why it matters
Potential benefit: If successful, participants could receive more effective, individualized risk reduction strategies for suicidal thoughts or behaviors.
How similar studies have gone: Previous studies have shown promise with multimodal approaches, but this project is among the first to combine multimodal data with dTMS in youth.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Diagnosis of mood disorder (major depressive episode, major depressive disorder, or bipolar disorder) according to DSM-5; * Age between 18 and 25 years; * Eligibility for magnetic resonance imaging; * Proficiency in the Italian language. Exclusion Criteria: * Comorbidity with severe neurological or medical conditions; * Diagnosis of cognitive impairment; * Inability to provide informed consent. For the control group: Inclusion Criteria: the same as the experimental group. Exclusion Criteria: * subjects with DSM-5 disorders * subjects with a family history of psychiatric disorders will be excluded.
Where it's running
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Fondazione Policlinico Universitario A. Gemelli IRCCS - UOC Psichiatria Clinica e d'Urgenza
Roma, Rm, Italy Recruiting
Study contacts
- Principal investigator: Delfina Janiri — Fondazione Policlinico Universitario Agostino Gemelli IRCCS
- Study coordinator: Delfina Janiri
- Email: delfina.janiri@unicatt.it
- Phone: +390630159527
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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.