Suicidal Ideation Clinical Trials

50 studies are recruiting for suicidal ideation in the United States right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.

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Studies, page 2

  1. Feasibility and Safety of Ketamine for Suicidal Patients in the Emergency Department

    There is currently no readily available pharmacologic intervention for suicidal ideation, a true psychiatric emergency, in the Emergency Department (ED). Investigators aim to trial low-dose, intravenous ketamine, a drug with well-established use in treatment-resistant depression, for patients who p…

    Stage
    Phase 1
    Ages
    18 to 65
    Site
    University of Kansas Medical Center Emergency Department, Kansas City, Kansas
    Locations
    2 in total
    Run by
    Lindsay Maguire, MD
  2. Frontal iTBS for Impulsivity and Suicidal Ideation in Veterans With Mild Traumatic Brain Injury

    The investigators hope to develop a treatment for suicidal ideation (SI), impulsivity and functional impairments (such as difficulties in social and work settings) that occur after a mild traumatic brain injury (mTBI). These conditions have been shown to be linked. The investigators are using a hig…

    Stage
    Phase 1
    Ages
    22 to 65
    Site
    Edward Hines Jr. VA Hospital, Hines, IL, Hines, Illinois
    Run by
    VA Office of Research and Development
  3. Flourish in Schools Pilot Study

    This study will test Flourish, a digital suicide prevention intervention for cyberbullied youth, within schools. Specifically, the study aims to: 1. Examine if Flourish is effective and can be feasibly delivered within schools among middle and high school students who are experiencing cyberbullying…

    Stage
    Not phased
    Ages
    11 to 21
    Site
    Bay Village School District, Bay Village, Ohio
    Locations
    2 in total
    Run by
    Candice Biernesser
  4. MicroRNA Correlates of Childhood Maltreatment and Suicidality

    This is a research study to find out if childhood trauma and stress are associated with depression or suicidal risk. The study will assess the effects of both short-term and long-term stress on biomarker (e.g. miRNA [MiRNA]) levels. miRNAs are a type of RNA (genetic material that is translated into…

    Stage
    Not phased
    Ages
    18 to 60
    Site
    University of Alabama at Birmingham, Birmingham, Alabama
    Locations
    2 in total
    Run by
    University of Alabama at Birmingham
  5. Brain Changes During Social Reward Psychotherapy for Mid- and Late-Life Suicidality

    The investigators hypothesized that during the 9-week course of Engage \& Connect treatment there will be an increase in brain functions of the Positive Valence System which in turn will lead to reduction in suicidality.

    Stage
    Not phased
    Ages
    50 to 80
    Site
    Weill Cornell Medicine, New York, New York
    Run by
    Weill Medical College of Cornell University
  6. Accelerated Intermittent Theta Burst Stimulation for Adolescent and Young Adult Depression With Elevated Suicide Risk

    The goal of this clinical trial is to learn if a fast-acting brain stimulation treatment called transcranial magnetic stimulation (TMS) can help people with depression and suicidal thoughts. The treatment is non-invasive (does not involve surgery or medications), is given over 5 days, and uses brai…

    Stage
    Not phased
    Ages
    15 to 25
    Site
    UC Davis Medical Center, Sacramento, California
    Run by
    University of California, Davis
  7. Cannabis, Linked Emotions, and Adolescent Risk Study

    The goal of this study is to disentangle relationships between acute cannabis use and withdrawal on proximal depression and suicide risk and recovery in adolescents ages 12-18 years by incorporating time-varying patterns of substance use, mood, and SI. This project aims to guide the development of …

    Stage
    Not phased
    Ages
    12 to 18
    Site
    Massachusetts General Hopsital, Boston, Massachusetts
    Run by
    Massachusetts General Hospital
  8. Augmenting Massed Cognitive Processing Therapy (CPT) to Prevent Suicide Risk Among Patients With PTSD

    The purpose of this research is to see if Crisis Response Planning (CRP), a brief strategy designed to help people cope effectively with emotional crises, combined with Cognitive Processing Therapy (CPT), a talk treatment for posttraumatic stress disorder (PTSD), will reduce suicidal thoughts and b…

    Stage
    Not phased
    Ages
    18 and older
    Site
    Carl R. Darnall Army Medical Center, Fort Hood, Texas
    Run by
    Ohio State University
  9. Efficacy, Effectiveness, and Implementation of Jaspr Health in Emergency Department- Part A

    This Study will comprehensively evaluate a multi-component suicide prevention technology (Jaspr Health) that facilitates delivery of suicided-related evidence-based practices (EBPs) while replacing wasted waiting time with productive time in the Emergency Departments (EDs). The EBPs satisfy several…

    Stage
    Not phased
    Ages
    18 and older
    Site
    UMass Memorial Health, Worcester, Massachusetts
    Run by
    University of Massachusetts, Worcester
  10. Assessment of Emotion Regulation Strategies Used When Suicidal

    Crisis Response Planning is an efficacious, one-session intervention that increases positive affect, decreases negative affect and psychiatric hospitalizations, and reduces suicide attempts by 76% among Servicemembers. Crisis Response Planning is hypothesized to reduce suicidality by identifying a …

    Stage
    Not phased
    Ages
    18 and older
    Site
    The Ohio State University Wexner Medical Center, Columbus, Ohio
    Run by
    Ohio State University
  11. Improving Outcomes in Adolescent Inpatient Depression With Deep Transcranial Magnetic Stimulation

    Evaluate the feasibility, safety, and preliminary efficacy of deep Transcranial Magnetic Stimulation (dTMS) as an adjunctive treatment for adolescents hospitalized with major depressive disorder (MDD).

    Stage
    Not phased
    Ages
    14 to 18
    Site
    Cincinnati Childrens Hospital Medical Center, Cincinnati, Ohio
    Run by
    Children's Hospital Medical Center, Cincinnati
  12. Targeting Adolescent Insomnia to Lessen Overall Risk of Suicidal Behavior

    This study will test the effectiveness of a sleep-related primary suicide prevention program entitled TAILOR (Targeting Adolescent Insomnia to Lessen Overall Risk of Suicidal Behavior), which includes specific behavior-change strategies for adolescents at risk of suicidal behavior who suffer from d…

    Stage
    Not phased
    Ages
    11 to 18
    Site
    Nationwide Children's Hospital, Columbus, Ohio
    Run by
    Jeff Bridge
  13. Teen Recovery Through Inspiration, Support, and Empowerment

    The goal of this pilot study is to test the effectiveness of a novel intervention for teenagers (ages 15-18) with mental health conditions who have been released from an acute care psychiatric facility. The intervention aims to reduce suicidality, depression, anxiety, re-hospitalization, and to imp…

    Stage
    Not phased
    Ages
    15 to 18
    Site
    The University of Texas Southwestern Medical Center, Dallas, Texas
    Run by
    University of Texas Southwestern Medical Center
  14. Randomized Clinical Trial of Re-Evaluating Suicidal Thoughts in Veterans

    Suicide prevention is a top priority for VA as all continue to seek new and inventive ways to reduce suicide rates among Veterans. Many experts agree that suicide prevention efforts could be improved by making suicide-specific interventions easier to access. The current project aims to move toward …

    Stage
    Not phased
    Ages
    18 and older
    Site
    Southeast Louisiana Veterans Health Care System, New Orleans, LA, New Orleans, Louisiana
    Run by
    VA Office of Research and Development
  15. Advancing Suicide Intervention Strategies for Teens During High Risk Periods

    To inform the effective management of adolescent suicide risk by evaluating promising treatments and developing the evidence-base for interventions that are well suited for widespread adoption, sustained quality, and impact.

    Stage
    Not phased
    Ages
    11 to 17
    Site
    Nationwide Children's, Columbus, Ohio
    Locations
    2 in total
    Run by
    Seattle Children's Hospital
  16. Preventing Suicide Among Sexual and Gender Diverse Young Adults in Primary Care

    The overall aim of this study is to reduce suicide among sexual and gender diverse youth ages 18-24 years old. This study will compare the effectiveness of two brief suicide prevention interventions that have been adapted for use with this population to use in primary care via telehealth and will r…

    Stage
    Not phased
    Ages
    18 to 24
    Site
    University of Pittsburgh, Pittsburgh, Pennsylvania
    Locations
    3 in total
    Run by
    Elizabeth Arnold
  17. Cortical Inhibition as a Biomarker of Response in a Comparison of Bilateral Versus Unilateral Accelerated Theta Burst Stimulation for Suicidal Ideation in Treatment-Resistant Depression -COMBAT-SI

    This is a prospective clinical trial to confirm the effectiveness of bilateral accelerated theta burst stimulation (aTBS) on suicidal ideation (SI), while exploring cortical inhibition measures in this treatment paradigm. In this proposed study, the investigators will evaluate the anti-suicidal eff…

    Stage
    Not phased
    Ages
    18 to 70
    Site
    UCSD Interventional Psychiatry, San Diego, California
    Run by
    University of California, San Diego
  18. Effect of Morning Light Exposure on Mood

    Mood dysregulation and suicidal ideation are closely associated with disruption of sleep and circadian rhythms. Moreover, sleep problems and circadian disruption are commonplace features of military life. Critically, specifically timed light exposure plays a powerful role in regulating mood, circad…

    Stage
    Not phased
    Ages
    18 to 60
    Site
    University of Arizona, Tucson, Arizona
    Run by
    University of Arizona
  19. Pilot of Reconnecting to Internal Sensations and Experiences in Undergraduates

    Project RISE is a randomized control trial. The intervention consists of four modules that focus on multiple aspects of interoception including: body awareness, body sensations/movement, eating, health and self-care, emotional awareness, and understanding the self in relation to others. The compara…

    Stage
    Not phased
    Ages
    18 to 65
    Site
    Auburn University, Auburn, Alabama
    Run by
    Auburn University
  20. Piloting a Culturally Adapted Suicide Prevention for Black Students in Chicago

    Suicide has been the third leading cause of death for Black youth in the U.S since the 1980s and persists as a leading cause of death for Black youth today. For example, in 2018 suicide was reported as the 2nd leading cause of death among Black Americans ages 10 to14 years old. Findings yielded fro…

    Stage
    Not phased
    Ages
    11 to 15
    Site
    University of Chicago, Chicago, Illinois
    Run by
    University of Chicago
  21. Stepped Approach to Reducing Risk of Suicide in Primary Care

    Suicide is the second leading cause of death among young people aged 12-17 years in the United States, yet many youth at risk for suicide are not identified or go untreated. Stepped care approaches have been shown to be effective at reducing suicide risk in clinical settings, including primary care…

    Stage
    Not phased
    Ages
    12 to 17
    Site
    AxessPointe Community Health Centers/Health Quarters, Akron, Ohio
    Locations
    15 in total
    Run by
    Cynthia Fontanella
  22. Feasibility, Acceptability, and Preliminary Efficacy of a Novel Personalized Mobile Intervention for Suicide - Open Trial (2)

    The primary aim of this grant is to conduct pilot testing on a novel personalized mobile intervention for suicide - Mobile Application to Prevent Suicide (MAPS) - and to establish feasibility, acceptability, safety, and primary outcomes (i.e., suicidal ideation and behavior; re-hospitalization).

    Stage
    Not phased
    Ages
    18 to 26
    Site
    Butler Hospital, Providence, Rhode Island
    Run by
    Butler Hospital
  23. Swift Outpatient Alternatives for Rapid Stabilization

    The goal of this clinical trial is to improve the effective outpatient management of acute youth suicide risk by optimizing intervention components to build an efficient, evidence-based intervention that is responsive to the needs of, and coordinated with, providers in primary care settings. The ma…

    Stage
    Not phased
    Ages
    13 to 21
    Site
    Seattle Children's, Seattle, Washington
    Run by
    University of Washington
  24. Therapeutic Evaluative Conditioning to Reduce Adolescents' Self-injurious Thoughts and Behaviors During and After Psychiatric Inpatient Hospitalization

    Suicide is the 2nd leading cause of death among adolescents, with the highest risk period for suicide being the month following psychiatric inpatient hospitalization. The investigators propose testing a brief, scalable intervention using evaluative conditioning aimed at reducing suicidal thoughts a…

    Stage
    Not phased
    Ages
    12 to 19
    Site
    Franciscan Hospital For Children, Inc., Brighton, Massachusetts
    Run by
    Franciscan Hospital For Children, INC.
  25. Suicide Treatment Alternatives for Teens

    Quasi-Randomized trial to compare inpatient care versus outpatient crisis intervention clinic. This study plans to enroll up to 1,000 participants across 4 sites in a 5 years period.

    Stage
    Not phased
    Ages
    12 to 18
    Site
    Northwell Health, Glen Oaks, New York
    Locations
    4 in total
    Run by
    Children's Hospital Medical Center, Cincinnati

How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.

What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.

Paid placement. Some studies pay us when someone asks to be connected to them. Those are labelled Sponsored wherever they appear, and they only appear when they match what you were actually looking for.