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.
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
- Conditions the study is for
- Suicidal Ideation, Suicide Attempt, Suicidal Behavior
- What is being tested?
- CAMS
- Type of treatment
- Lifestyle or therapy programme
- 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
- Are there results?
- Not yet: the study is under way
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
Show all 10Show fewer
- 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.
United States1 site
The Cleveland Clinic
Cleveland, Ohio, 44195
Tatiana Falcone, M.D., (216) 444-7459, falcont1@ccf.org
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:
- 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.
- Conditions
- Suicidal Ideation, Suicide Attempt, Suicidal Behavior, Depression / Major Depressive Disorder, Hopelessness, Neurobiological
- 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 group | Role | What they receive |
|---|---|---|
| High risk (HR) | Active comparator | patients 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 intervention | patients with 1 year history of SI with no attempts |
| Minimal risk (MinR) | No intervention | age-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.
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)
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.
- First posted5 May 2026
- Study start30 Oct 2026 (estimated)
- Primary completion1 Sep 2031 (estimated)
- Study completion1 Oct 2031 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Suicidal IdeationStudies of the same condition, open and under way.
- More trials run by The Cleveland ClinicThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- The Cleveland Clinic
- Sponsor type
- University, hospital or other
- Collaborators
- MQ Mental Health Research
- Responsible party
- Principal investigator, Tatiana Falcone, MD, The Cleveland Clinic
- Investigators
- Tatiana Falcone, M.D., Principal investigator, The Cleveland Clinic
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
Study at a glance
From the registry record, last updated by the sponsor on 3 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Neural Correlates of Suicidal Behavior in Youth: a Pre and Post CAMS Therapy Neuroimaging Study
- ClinicalTrials.gov ID
- NCT07568054
- Acronym / sponsor ID
- IRB 25-894
- Conditions
- Suicidal Ideation, Suicide Attempt, Suicidal Behavior, Depression / Major Depressive Disorder, Hopelessness, Neurobiological
- Keywords
- Suicidal ideation, Suicide attempt, Suicidal behavior, Youth suicide, Depression, Hopelessness, CAMS therapy, Neuroimaging
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 60 participants (estimated)
- Lead sponsor
- The Cleveland ClinicUniversity, hospital or other
- Collaborators
- MQ Mental Health Research
- Study start
- 30 Oct 2026 (estimated)
- Primary completion
- 1 Sep 2031 (estimated)
- Study completion
- 1 Oct 2031 (estimated)
- First posted
- 5 May 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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:
- 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.
Study design
- Primary purpose
- Health services research
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 3
- 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.
| Arm | Type | Receives |
|---|---|---|
| High risk (HR) | Active comparator | Behavioral: CAMSpatients discharged within 1 week from the hospital for a SA and with a history of 2 previous SAs |
| Medium risk (MedR) | No intervention | –patients with 1 year history of SI with no attempts |
| Minimal risk (MinR) | No intervention | –age-matched controls with no prior history of SI or behavior, not taking any psychotropic medication and no family history of suicide |
Who may qualify
- Ages
- 14 to 24 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult
Key inclusion criteria (7 listed)
- Subjects must be 14-24 years old
- Subjects must be:
- Subjects must have the ability to understand and the willingness to sign a written informed consent/assent document
- Subjects must be English speaking
Key exclusion criteria (10 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| CAMSCAMS 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). | Behavioural | High risk (HR) |
Primary outcome
MRS & suicidality
Time frame: 5 years
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.
1 secondary outcome
MRS & suicidality
Time frame: 5 years
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 3 Sep 2026.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Tatiana Falcone, M.D. principal investigator
The Cleveland Clinic
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing CAMS in people with Suicidal Ideation and Suicide Attempt, run by The Cleveland Clinic at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 7 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 3 Sep 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Christina A Deisz, LISW-S ((440) 225-6193, deiszc@ccf.org), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
MRS & suicidality (time frame: 5 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Sep 2026.