[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"suicide-attempts\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:suicide-attempts":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,47,77,110],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":4},"100639344","phase-3-brief-cognitive-behavioral-therapy-for-suicide-prevention-in-a-brazilian-sample-a-study-protocol-of-a-randomized-clinical-trial-100639344",false,"NCT07574658","Brief Cognitive Behavioral Therapy for Suicide Prevention in a Brazilian Sample: a Study Protocol of a Randomized Clinical Trial","Study participants meet inclusion criteria if they are (1) Between the ages of 18-65; (2) Treatment-seeking status in outpatient mental health and\u002F or inpatient psychiatry discharge; (3) Report current (within the past week) suicide ideation (e.g., score greater than 2 on the Scale for Suicide Ideation) and\u002For a suicide attempt within the past month (e.g., as assessed by the Beck Scale for Suicide Ideation (BSI); (4) Able to understand and speak Portuguese; (5) Able to complete the informed consent process.","ALL","18 Years","60 Years",{"count":19,"type":20},150,"ESTIMATED","INTERVENTIONAL",[23],"PHASE3","The vast majority of suicides occur in low-and middle-income countries (LMICs), and evidence on effective psychotherapeutic interventions to prevent suicide that are culturally adapted to these contexts is limited. This scenario implies an urgent need for evidence-based suicide prevention strategies in Brazil. This research aims to evaluate the effectiveness of brief cognitive-behavioral therapy in preventing suicide in an outpatient setting of a Brazilian university. A randomized, controlled clinical trial with two arms, whose participants are adults who have attempted suicide or have had suicidal ideation with intent to die, will be designed. Inclusion criteria will be suicidal ideation with intent to die in the last week and\u002For suicide attempt in the last month. Patients will be randomly assigned to receive either a weekly 12-session supportive therapy or brief cognitive-behavioral therapy. The duration of treatment will be approximately 3 months. Both groups will have weekly individual therapy. Follow-up contact will be made 1 month and 6 months after treatment. If necessary, patients are entitled to two booster sessions during the follow-up period. The outcomes to be assessed, a priori, are suicide attempts, self-harm without suicidal intent and suicidal ideation, assessed by the Beck Scale for Suicide Ideation (BSI). Linear mixed models will be used to assess the outcomes of continuous variables, logistic regression models for categorical outcomes and survival analysis for the analysis of suicide attempts.",[26,27],"Suicide Ideation","Suicide Attempts",[29,30,31,32,33,34],"Suicide","Suicide prevention","Brief Cognitive Behavioral Therapy (BCBT)","Randomized clinical trial","Evidence-based psychotherapy","Low- and middle-income countries (LMICs)","NOT_YET_RECRUITING","2026-05-04",{"date":38,"type":39},"2026-05-08","ACTUAL",{"date":41,"type":20},"2026-05-10",{"date":43,"type":20},"2028-07-10",{"name":45,"class":46},"University of Sao Paulo","OTHER",{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":54,"sex":15,"minAge":55,"maxAge":56,"enrollmentInfo":57,"targetDuration":4,"studyType":21,"phases":59,"briefSummary":61,"conditions":62,"keywords":4,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":76},"100445325","advancing-suicide-intervention-strategies-for-teens-during-high-risk-periods-100445325","NCT05078970","Advancing Suicide Intervention Strategies for Teens During High Risk Periods","ASSIST","Inclusion Criteria:\n\n1. Provision of signed and dated informed consent form\n2. Youth, aged 11-17\n3. Endorse suicidal ideation and\u002For behavior\n4. Admitted to acute care (emergency, inpatient medical or inpatient psychiatric) due to suicidality\n\nExclusion Criteria:\n\n1. Presence of psychosis, intellectual disability, autism spectrum disorder, eating disorder with unstable vitals\n2. Limited English proficiency that would interfere with the ability to complete study assessments",true,"11 Years","17 Years",{"count":58,"type":20},306,[60],"NA","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.",[27,63,64,65],"Suicidal Ideation","Suicide and Self-harm","Suicide Threat","RECRUITING","2025-11-13",{"date":69,"type":39},"2025-11-14",{"date":71,"type":39},"2022-08-11",{"date":73,"type":20},"2027-01-31",{"name":75,"class":46},"Seattle Children's Hospital",2,{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":83,"eligibilityCriteria":84,"healthyVolunteers":54,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":85,"targetDuration":4,"studyType":21,"phases":87,"briefSummary":88,"conditions":89,"keywords":94,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":103,"completionDateStruct":105,"leadSponsor":107,"locationsCount":109},"100593929","couple-based-crisis-safety-planning-100593929","NCT07012824","Couple-Based Crisis Safety Planning","Couple-Based Crisis Response Planning for Veterans","CRP-C","Inclusion Criteria:\n\n* (At least) One participant from the couple must have Veteran status\n* Currently resides in Georgia\n* English speaking\n* The Veteran must own a smartphone\n* Veteran must have experienced crisis symptoms in the past three months. At least 1 symptom of entrapment, and at least 1 symptom from 2 of the associated disturbance categories \\[i.e. affective disturbance, loss of cognitive control, hyperarousal, or social withdrawal\\]\n* Currently be in a committed relationship for at least one year\n* The Veteran must be able to present a copy of DD form 214 (Certificate of Release or Discharge from Active Duty issued by the U.S. Department of Defense)\n\nExclusion Criteria:\n\n* Non-English speaking\n* Under 18 years of age\n* Resides in a different state than Georgia\n* Either partner reports injury or fear resulting from intimate partner violence in the past three months.\n* Participants who meet study criteria for imminent suicide risk Depressive Symptom Index - Suicidality Subscale (Joiner et al., 2002), defined as a DSI- SS score of 7 or greater, or selecting \"3\" on items B \\[formulated plan\\] or D \\[constant urge to kill self (I. H. Stanley et al., 2021)",{"count":86,"type":20},100,[60],"Suicide is a leading cause of death in Veterans. Suicide rates among Veterans have increased approximately 36% from 2001 to 2020. Veterans are at increased risk for suicide compared to non-Veterans, with the rate of suicide death being 57.3% higher for Veterans than non-Veterans. The present study will pilot test a virtual couple-based crisis response plan (CRP-C) for Veterans in order to reduce crisis symptoms and decrease suicide risk.",[90,63,91,27,92,93],"Suicidal Ideas","Crisis; Emotional","Suicidal and Self-injurious Behaviour","Suicidal Impulses",[95,96,97,98,99],"Veteran safety","Suicide risk","Crisis safety plan","Suicide crisis","intervention","2025-06-08",{"date":102,"type":39},"2025-06-10",{"date":104,"type":20},"2025-06",{"date":106,"type":20},"2027-08",{"name":108,"class":46},"University of Georgia",1,{"id":111,"slug":112,"hasResults":11,"nctId":113,"briefTitle":114,"officialTitle":114,"acronym":115,"eligibilityCriteria":116,"healthyVolunteers":11,"sex":15,"minAge":117,"maxAge":118,"enrollmentInfo":119,"targetDuration":4,"studyType":21,"phases":121,"briefSummary":122,"conditions":123,"keywords":4,"overallStatus":66,"whyStopped":4,"lastUpdateSubmitDate":125,"lastUpdatePostDateStruct":126,"startDateStruct":128,"completionDateStruct":130,"leadSponsor":132,"locationsCount":109},"100500459","therapeutic-evaluative-conditioning-to-reduce-adolescents-self-injurious-thoughts-and-behaviors-during-and-after-psychiatric-inpatient-hospitalization-100500459","NCT05796531","Therapeutic Evaluative Conditioning to Reduce Adolescents' Self-injurious Thoughts and Behaviors During and After Psychiatric Inpatient Hospitalization","TEC","Inclusion Criteria:\n\n* Be a patient on McLean-Franciscan Child and Adolescent Inpatient Program (MF-CAIP) of Franciscan Children's (FC)\n* Be 12-19 years-old\n* Own a smartphone\n* Have a parent\u002Fguardian that can provide permission\n* Child can assent\n* Presentation to the hospital with non-suicidal self-injury (NSSI), suicidal ideation or a suicide attempt.\n\nExclusion Criteria:\n\n* Any factor that impairs an individual's ability to comprehend and effectively participate in the study, including\n* an inability to speak or write English fluently\n* the presence of gross cognitive impairment due to florid psychosis, intellectual disability, dementia, acute intoxication, etc., or the presence of extremely agitated or violent behavior\n* a potential discharge location anticipated to be a residential program in which the average length of stay is more than 14 days","12 Years","19 Years",{"count":120,"type":20},155,[60],"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 and behaviors among adolescents during and after inpatient hospitalization. Scalable interventions, such as the one proposed that reduce suicide risk during this markedly high-risk period, could result in large-scale decreases in suicide death.",[124,63,27],"Self-Injurious Behavior","2024-07-10",{"date":127,"type":39},"2024-07-12",{"date":129,"type":39},"2023-03-31",{"date":131,"type":20},"2026-12-31",{"name":133,"class":46},"Franciscan Hospital For Children, INC."]