- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07568054
Neural Correlates of Suicidal Behavior in Youth
Neural Correlates of Suicidal Behavior in Youth: a Pre and Post CAMS Therapy Neuroimaging Study
This study, titled "Neural Correlates of Suicidal Behavior in Youth: a Pre and Post CAMS Therapy Neuroimaging Study," aims to better understand the brain mechanisms underlying suicidal thoughts and behaviors in adolescents and young adults (ages 14-24). Suicide is a leading cause of death in this population, and current clinical approaches often fail to accurately predict or prevent suicidal behavior. This study seeks to identify objective neurobiological markers associated with suicide risk and treatment response.
Participants will be divided into three groups: (1) high-risk individuals recently hospitalized following a suicide attempt, (2) medium-risk individuals with chronic suicidal ideation but no attempts, and (3) low-risk healthy controls. All participants will undergo advanced neuroimaging, including magnetoencephalography (MEG) and magnetic resonance imaging (MRI), along with comprehensive psychiatric assessments.
The study focuses on brain regions and networks implicated in suicidality, including the anterior cingulate cortex and salience network, as well as neurochemical markers such as glutamate. It also examines electrophysiological activity and functional connectivity patterns associated with suicidal thoughts and behaviors.
High-risk participants will receive an evidence-based psychotherapy called the Collaborative Assessment and Management of Suicidality (CAMS). This therapeutic approach emphasizes collaboration between patient and clinician to identify and address the underlying drivers of suicidal thoughts, with a focus on increasing hope and reducing psychological distress. Neuroimaging and clinical assessments will be repeated after completion of CAMS to evaluate treatment-related changes.
The study's primary goals are to:
- Identify neural and electrophysiological correlates of suicide risk.
- Distinguish biological differences between individuals with suicidal ideation and those who have attempted suicide.
- Determine how CAMS therapy affects brain function and neurochemistry.
By integrating clinical and neurobiological data, this research aims to improve understanding of suicidality, enhance risk prediction, and inform more effective, personalized interventions for at-risk youth.
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
This research study, titled "Neural Correlates of Suicidal Behavior in Youth: a Pre and Post CAMS Therapy Neuroimaging Study," is designed to advance understanding of the neurobiological and clinical mechanisms underlying suicidal thoughts and behaviors in adolescents and young adults aged 14-24 years. Suicide is one of the leading causes of death in this age group, and current clinical tools are often insufficient for accurately predicting risk or preventing future suicide attempts. A major limitation in the field is the lack of objective biological markers that can identify individuals at highest risk and guide targeted treatment.
The overarching goal of this study is to investigate how brain structure, function, and neurochemistry differ across varying levels of suicide risk, and how these features change following an evidence-based suicide-specific psychotherapy. The study combines advanced neuroimaging techniques with detailed clinical assessments to provide a comprehensive, multimodal understanding of suicidality.
Participants will be divided into three groups (n=60 total, 20 per group):
- High Risk (HR): Individuals recently hospitalized following a suicide attempt and with a history of multiple attempts.
- Medium Risk (MedR): Individuals with chronic suicidal ideation lasting at least one year but no history of attempts.
- Minimal Risk (MinR): Healthy controls with no history of suicidal ideation or behavior and no psychiatric treatment.
All participants will complete baseline assessments including structured psychiatric interviews and validated rating scales measuring depression, hopelessness, suicidal ideation, and overall functioning. Neuroimaging will include magnetoencephalography (MEG) to measure real-time brain activity and MRI-based techniques such as resting-state functional MRI (rsfMRI), magnetic resonance spectroscopy (MRS), and task-based imaging focused on episodic future thinking.
The study specifically targets brain regions and networks implicated in suicide risk, including the anterior cingulate cortex (ACC), anterior insula (AI), salience network, and default mode network. These regions are associated with emotional regulation, self-referential thinking, and processing of future-oriented thoughts. Prior research suggests that abnormalities in these systems-such as altered connectivity, metabolic imbalances (e.g., glutamate levels), and disrupted electrophysiological patterns-may contribute to suicidal ideation and behavior.
A key component of the study is the examination of hopelessness, which is considered a central psychological factor in suicidality and a potential proxy for suicide risk. The study will explore how neural markers correlate with levels of hopelessness and how these relationships differ across risk groups.
Following baseline assessments, participants in the high-risk group will receive the Collaborative Assessment and Management of Suicidality (CAMS) intervention. CAMS is a structured, evidence-based psychotherapy that emphasizes collaboration between the patient and clinician to identify the personal drivers of suicidal thoughts. It uses the Suicide Status Form (SSF) to guide assessment, treatment planning, and ongoing monitoring. Core principles of CAMS include empathy, collaboration, honesty, and a direct focus on suicidality. Treatment typically involves weekly sessions and continues until the patient demonstrates reduced suicide risk and improved coping.
After completing CAMS therapy (typically 3-12 sessions), high-risk participants will undergo repeat neuroimaging and clinical assessments. This pre-post design allows researchers to evaluate how psychotherapy influences brain function, connectivity, and neurochemical markers, as well as clinical symptoms such as hopelessness and suicidal ideation.
The study has three primary aims:
- To identify electrophysiological markers of suicidality using MEG, including oscillatory dynamics and network connectivity patterns.
- To examine neuroimaging correlates of suicide risk, including functional connectivity, brain activation during future thinking tasks, and metabolic measures obtained through MRS.
- To assess the effects of CAMS therapy on brain function and neurochemistry in high-risk individuals.
In addition to the main study, qualitative focus groups will be conducted with adolescents participating in an intensive outpatient program. These groups aim to gather patient perspectives on barriers to research participation and treatment engagement, helping to improve study design and clinical care approaches.
Data analysis will include comparisons across risk groups using statistical models such as ANOVA and regression analyses, as well as correlation analyses to examine relationships between clinical measures and neurobiological variables. Longitudinal analyses will evaluate changes following CAMS therapy.
The potential impact of this study is significant. By identifying objective neural markers associated with suicide risk and treatment response, the research could improve early detection of high-risk individuals and guide personalized interventions. Understanding how CAMS therapy produces changes in the brain may also help refine and optimize treatment strategies for suicidal youth.
Ultimately, this study aims to bridge the gap between clinical psychiatry and neuroscience, contributing to more effective, biologically informed approaches to suicide prevention in young people.
Tipo di studio
Iscrizione (Stimato)
Fase
- Non applicabile
Contatti e Sedi
Contatto studio
- Nome: Tatiana Falcone, M.D.
- Numero di telefono: (216) 444-7459
- Email: falcont1@ccf.org
Backup dei contatti dello studio
- Nome: Christina A Deisz, LISW-S
- Numero di telefono: (440) 225-6193
- Email: deiszc@ccf.org
Luoghi di studio
-
-
Ohio
-
Cleveland, Ohio, Stati Uniti, 44195
- The Cleveland Clinic
-
Contatto:
- Tatiana Falcone, M.D.
- Numero di telefono: (216) 444-7459
- Email: falcont1@ccf.org
-
-
Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
- Bambino
- Adulto
Accetta volontari sani
Descrizione
Inclusion Criteria:
- Subjects must be 14-24 years old
Subjects must be:
- High Risk Subjects: Psychiatrically admitted due to a suicide attempt or history of 2 previous suicide attempts
- Medium Risk Subjects: Suicide ideation for the past year with no suicide attempt
- Minimal Risk Subjects: No previous history of suicidal ideation or behavior, not taking any psychiatric history or medication, and no family history of suicide
- Subjects must have the ability to understand and the willingness to sign a written informed consent/assent document
- Subjects must be English speaking
Exclusion Criteria:
- Subjects with known history of Autism Spectrum Disorder; non-verbal patients
- Subjects with moderate or severe intellectual disability (IQ less than 70 and those patients in special education classes full time)
- Subjects with Schizophrenia or history of any type of psychosis including mood related psychosis and brief reactive psychosis
- Within 6 months before initial screening, urine toxicology positive for phencyclidine, cocaine or amphetamines (subjects prescribed amphetamines for the management of ADHD will not be excluded)
- Subjects with a history of moderate or severe substance or alcohol use per DSM-5 criteria in the past 6 months
- Subjects who are currently pregnant or breastfeeding
- Subjects in custody of Children's Services
- Subjects with recent bone, tendon, spine or joint surgery
- Subjects with recent metallic dental implants
- Subjects weighing less than 30 kg or more than 200 kg
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Ricerca sui servizi sanitari
- Assegnazione: Non randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
|
Comparatore attivo: High risk (HR)
patients discharged within 1 week from the hospital for a SA and with a history of 2 previous SAs
|
CAMS weekly sessions will be started immediately as an inpatient at the start of the study for the high risk participants.
CAMS will be continued weekly after the patient is discharged and followed up as an outpatient.
Weekly CAMS sessions will be terminated after the subject, as an outpatient, has three consecutive outpatient CAMS sessions with an overall risk < 2 (# 6 on the SSF Core Assessment) along with a positive response regarding their thoughts/feelings and clinician indicating behavioral stability (suicidal behavior).
|
|
Nessun intervento: Medium risk (MedR)
patients with 1 year history of SI with no attempts
|
|
|
Nessun intervento: Minimal risk (MinR)
age-matched controls with no prior history of SI or behavior, not taking any psychotropic medication and no family history of suicide
|
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
MEG and suicidality
Lasso di tempo: 5 years
|
Measure the difference on the connectivity within the salience network.
This will be quantified using phase-locking values (PLV) across different frequency bands in 10-second intervals.
The average PLV-based connectivity will serve as an electrophysiological biomarker for correlation with SI.
To test hypothesis 1, salience network connectivity will be compared between groups using ANOVA.
|
5 years
|
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Suicidality & network connectivity
Lasso di tempo: 5 years
|
To study the relationship of suicidality with network connectivity, activation during an episodic future thinking task, and MRS measures. To test this, activation strength of the ventral medial prefrontal cortex will be tested using a between-group ANOVA. Using the MRS voxel locations as a guide, functional connectivity between the pregenual anterior cingula cortex and anterior insula will be calculated. Glutamine and myo-inositol levels and rsfMRI strength will be compared using between-group ANOVAs. |
5 years
|
Altre misure di risultato
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
CAMS on MEG and MRS metabolites
Lasso di tempo: 5 years
|
To investigate the the changes of Baseline SSF scoring before and after CAMS on MEG and MRS metabolites in the HR group.
MRS measures of Glutamine and myo-inositol and MEG salience network measures will be tested using a repeated measures ANOVA.
To test this, the change in Glutamine and myo-inositol levels will be calculated and correlated with measures of hopelessness and SI using the Beck Hopelessness Scale and Optimism and Hope scale along with the Beck SSI.
|
5 years
|
Collaboratori e investigatori
Sponsor
Collaboratori
Investigatori
- Investigatore principale: Tatiana Falcone, M.D., The Cleveland Clinic
Studiare le date dei record
Studia le date principali
Inizio studio (Stimato)
Completamento primario (Stimato)
Completamento dello studio (Stimato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- IRB 25-894
Piano per i dati dei singoli partecipanti (IPD)
Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .
Prove cliniche su CAMS
-
Evidence-Based Practice Institute, Seattle, WAUniversity of Florida; The Catholic University of AmericaCompletato
-
Louisville VA Medical CenterRocky Mountain MIRECC for Suicide PreventionCompletato
-
Nationwide Children's HospitalThe Catholic University of AmericaTerminatoIdeazione suicida | Suicidio, tentatoStati Uniti
-
Evidence-Based Practice Institute, Seattle, WAMayo Clinic; Aurora Health Care; The Catholic University of America; Harborview Injury... e altri collaboratoriCompletatoSuicidioStati Uniti
-
Duke UniversityNational Institute of Mental Health (NIMH)Completato
-
University of WashingtonNational Institute of Mental Health (NIMH)ReclutamentoIdeazione suicida | Tentativo di suicidioStati Uniti
-
Seattle Children's HospitalNationwide Children's HospitalReclutamentoIdeazione suicida | Minaccia di suicidio | Suicidio e autolesionismo | Tentativi di suicidioStati Uniti
-
China National Biotec Group Company LimitedPeking University; Shaanxi Provincial Center for Disease Control and Prevention; Changchun Institute of Biological Products Co., Ltd... e altri collaboratoriSconosciuto
-
Tatiana Falcone, MDNational Institute of Mental Health (NIMH); Massachusetts General Hospital; National...Reclutamento