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Suicidal IdeationNCT07568054

Neural Correlates of Suicidal Behavior in Youth

A study testing CAMS in people with Suicidal Ideation and Suicide Attempt, run by The Cleveland Clinic at 1 site in United States.

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Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

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Official record

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Trial summary

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). Read more about this study

Who is it for?
Ages 14 to 24 yearsHealthy volunteers can take part
What is being tested?
CAMS
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 siteUnited States
Study dates
30 Oct 2026to 1 Oct 2031
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 14 to 24 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult

Who may be able to join

  • 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

Who cannot join

  • 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
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  • 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

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Christina A Deisz, LISW-S contact

(440) 225-6193

deiszc@ccf.org

Tatiana Falcone, M.D. contact

(216) 444-7459

falcont1@ccf.org

United States1 site
  • The Cleveland Clinic

    Cleveland, Ohio, 44195

    Tatiana Falcone, M.D., (216) 444-7459, falcont1@ccf.org

Other trials in United States

About this study

Official title: 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.

Read more

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.

Read the detailed description

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:

  1. To identify electrophysiological markers of suicidality using MEG, including oscillatory dynamics and network connectivity patterns.
  2. To examine neuroimaging correlates of suicide risk, including functional connectivity, brain activation during future thinking tasks, and metabolic measures obtained through MRS.
  3. 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.

Being tested
CAMS
Keywords
Suicidal ideation, Suicide attempt, Suicidal behavior, Youth suicide, Depression, Hopelessness, CAMS therapy, Neuroimaging
Medical subject headings
Suicidal Ideation, Suicide, Attempted, Depression, Depressive Disorder, Major

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • CAMSBehavioural

    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).

Study groups in NCT07568054
Study groupRoleWhat they receive
High risk (HR)Active comparatorpatients discharged within 1 week from the hospital for a SA and with a history of 2 previous SAs
Receives: Behavioral: CAMS
Medium risk (MedR)No interventionpatients with 1 year history of SI with no attempts
Minimal risk (MinR)No interventionage-matched controls with no prior history of SI or behavior, not taking any psychotropic medication and no family history of suicide

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. MRS & suicidality

    To investigate the effect of changes in Suicide Status Form (SSF) scores (low severity 1-5 high severity) as a result of CAMS therapy on Glx levels.

    Measured: 5 years

Secondary outcomes (1)
  1. MRS & suicidality

    To investigate the effect of changes in Suicide Status Form (SSF) scores (low severity 1-5 high severity) as a result of CAMS therapy on myo inositol levels.

    Measured: 5 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 May 2026
  2. Study start30 Oct 2026 (estimated)
  3. Primary completion1 Sep 2031 (estimated)
  4. Study completion1 Oct 2031 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Non-randomised
Intervention model
Parallel groups
Model description
This study uses a parallel-group design with three cohorts (high, medium, and minimal suicide risk) to examine neurobiological correlates of suicidality in youth (ages 14-24). All participants undergo baseline clinical assessments and neuroimaging (MEG, MRI, fMRI, MRS) to compare brain function, connectivity, and neurochemistry across risk groups. The high-risk group additionally receives the Collaborative Assessment and Management of Suicidality (CAMS) intervention and completes follow-up assessments after treatment. This allows for both cross-sectional comparisons between groups and longitudinal evaluation of treatment-related changes. The study aims to identify biomarkers of suicide risk and predictors of therapeutic response.
Masking
None (open label)
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07568054
Sponsor's protocol ID
IRB 25-894
Status last verified
Sep 2026
First submitted
10 Apr 2026
Last updated
3 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

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