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Suicidal Ideation clinical trials

View clinical trials related to Suicidal Ideation.

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NCT ID: NCT03114917 Completed - Psychosis Clinical Trials

Cognitive AppRoaches to coMbatting Suicidality

CARMS
Start date: May 12, 2017
Phase: N/A
Study type: Interventional

This is a randomised controlled trial which investigates the effectiveness of CARMS (Cognitive AppRoaches to coMbatting Suicidality) therapy in reducing suicidal thoughts and how well CARMS works in practice within the NHS. The trial will compare two groups of people with psychosis who are using NHS mental health services. One group will carry on with their usual treatment. The other group will be offered 24 weekly sessions of CARMS therapy, plus their usual treatment.

NCT ID: NCT03097133 Completed - Clinical trials for Depressive Disorder, Major

54135419SUI3002: A Study to Evaluate the Efficacy and Safety of Intranasal Esketamine in Addition to Comprehensive Standard of Care for the Rapid Reduction of the Symptoms of Major Depressive Disorder, Including Suicidal Ideation, in Adult Participants Assessed to be at Imminent Risk for Suicide

Aspire II
Start date: June 15, 2017
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy of intranasal esketamine 84 milligram (mg) compared with intranasal placebo in addition to comprehensive standard of care in reducing the symptoms of Major Depressive Disorder (MDD), including suicidal ideation, in participants who are assessed to be at imminent risk for suicide, as measured by the change from baseline on the Montgomery-Asberg Depression Rating Scale (MADRS) total score at 24 hours post first dose.

NCT ID: NCT03092271 Completed - Suicide Clinical Trials

Randomized Trial of Stepped Care for Suicide Prevention in Teens and Young Adults

Step2Health
Start date: April 3, 2017
Phase: N/A
Study type: Interventional

This randomized controlled trial will evaluate two approaches to achieving the aspirational goal of Zero Suicide within a health system: 1) Zero Suicide Best Practices initiated through a zero suicide quality improvement initiative within a health system; and 2) Zero Suicide Best Practices plus an innovative stepped care for suicide prevention intervention for adolescents and young adults that matches treatment intensity with risk levels for suicide/self-harm. ..

NCT ID: NCT03080168 Completed - Suicidal Ideation Clinical Trials

The "AIM Study": Investigating Whether Actigraphy and Ideation Measures Can Promote Patient Safety

AIM
Start date: February 21, 2017
Phase:
Study type: Observational

This is a research project looking at whether measuring movements or responses to certain questions can help predict suicidal thoughts or actions. This project has two parts: The first part will occur while the participant is receiving hospitalized at the Bedford VA Hospital. It involves wearing a watch-like device on his/her wrist and answering questions or doing tasks to measure mood and other mental health symptoms, and suicidal thoughts. In the second phase, the investigators will call the participant around 12 months after s/he has left the hospital. The investigators will discuss how s/he is doing and if s/he has had suicidal thoughts or made suicidal acts.

NCT ID: NCT03039192 Completed - Clinical trials for Depressive Disorder, Major

54135419SUI3001: A Study to Evaluate the Efficacy and Safety of Intranasal Esketamine in Addition to Comprehensive Standard of Care for the Rapid Reduction of the Symptoms of Major Depressive Disorder, Including Suicidal Ideation, in Adult Participants Assessed to be at Imminent Risk for Suicide

Aspire I
Start date: June 9, 2017
Phase: Phase 3
Study type: Interventional

The purpose of the study is to evaluate the efficacy of intranasal esketamine 84 milligram (mg) compared with intranasal placebo in addition to comprehensive standard of care in reducing the symptoms of Major Depressive Disorder (MDD), including suicidal ideation, in participants who are assessed to be at imminent risk for suicide, as measured by the change from baseline on the Montgomery-Asberg Depression Rating Scale (MADRS) total score at 24 hours post first dose.

NCT ID: NCT03016572 Completed - Anxiety Disorders Clinical Trials

Promote Access to Stop Suicide: Comparison of Follow up Services for Youth at Risk for Suicide

PASS
Start date: May 4, 2017
Phase: N/A
Study type: Interventional

This research study is designed to answer specific questions about new ways to provide services for youth at-risk of suicide.

NCT ID: NCT03014518 Completed - Suicide Clinical Trials

Biomarkers as Predictors of Suicidal Risk in Adolescents

Start date: December 2016
Phase:
Study type: Observational

Suicide is one of the most devastating events in society at all levels. The primary goal of this study is to predict suicide in adolescents at risk. We will utilize blood biomarker measurement and clinical risk factor scales to develop a tool to identify adolescents at risk for suicide earlier, which will allow clinicians to prescribe timely treatment and prevent suicide.

NCT ID: NCT03014362 Completed - Suicide Clinical Trials

TMS for Suicidal Crisis in Active Duty SMs

TMS4SI
Start date: June 12, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if the use of Transcranial Magnetic Stimulation (TMS) provides rapid reduction and sustained attenuation of suicidal crisis. TMS is a treatment for suicidal crisis that is quicker, less invasive, better tolerated, and with fewer side effects than current treatments such as Electroconvulsive Therapy (ECT) and medication therapies. There will be 6 months of follow-up, in order to establish the ongoing and lasting therapeutic effect of TMS.

NCT ID: NCT02997722 Terminated - Suicidal Ideation Clinical Trials

The Effect of Ketamine on the Length of Hospital Stay of Patients Hospitalized With Suicidal Ideation.

Start date: March 2, 2017
Phase: Phase 4
Study type: Interventional

This study will evaluate the effect of ketamine on the treatment of patients hospitalized with suicidal thoughts. Half of the patients will receive one dose of ketamine in the vein. The other half will receive a placebo. Because we think that ketamine will improve depression and suicidal thoughts, we expect that patients who receive ketamine will require less time in the hospital than patients who receive placebo.

NCT ID: NCT02986113 Completed - Suicidal Ideation Clinical Trials

Men and Providers Preventing Suicide (MAPS)

Start date: December 2016
Phase: N/A
Study type: Interventional

This study will determine if suicidal middle-aged men who use a personalized computer program addressing suicide risk before a primary care visit are more likely to discuss suicide and accept treatment, reducing their suicide preparatory behaviors and thoughts.This is important because half of all men who die by suicide visit primary care within a month of death, yet few broach the topic, missing chances for prevention.