[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"suicide-threat\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:suicide-threat":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,45,73,97],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100506777","written-exposure-therapy-for-suicide-prevention-100506777",false,"NCT05878795","Written Exposure Therapy for Suicide Prevention","Written Exposure Therapy for Suicide Prevention (WET-SP)","Inclusion Criteria:\n\n* Current active duty military service member, veteran, and beneficiaries\n* Admitted to Carl R. Darnall Army Medical Center (CRDAMC) for suicidal thoughts, a suicide plan, or a suicide attempt\n* Elevated levels of suicidal ideation severity in the past two weeks, as indicated by a score \\>= 3 on the Depressive Symptom Index-Suicidality Subscale (DSI-SS)\n* Ability to read, write, and speak English\n\nExclusion Criteria:\n\n* Active psychosis as the priority of care for hospitalization\n* Moderate or greater cognitive impairment (as determined by the inability to comprehend the baseline screening questionnaires)\n* Unable to provide informed consent","ALL","18 Years",{"count":19,"type":20},160,"ESTIMATED","INTERVENTIONAL",[23],"NA","Military service members admitted to inpatient psychiatry for self-injurious thoughts and behaviors (SITBs) represent an at-risk group for continued SITBs and rehospitalizations in the post-discharge period. However, there is an absence of evidence-based interventions designed to be delivered on inpatient psychiatric units to reduce the risk of post-discharge SITBs. To address this gap, the investigator's research group developed Written Exposure Therapy for Suicide Prevention (WET-SP), a brief, scalable, suicide-specific psychotherapy based on the written disclosure paradigm. Written disclosure, in which an individual writes about a personally stressful experience and the related thoughts and feelings, yields improvements across physical and psychiatric domains. Pilot data suggest that written exposure also yields reductions in SITBs. Yet, no study has adapted the written exposure paradigm specifically to target the amelioration of distress associated with suicidal crises and examined whether implementing WET-SP reduces the risk of subsequent SITBs and suicide-related hospitalizations.\n\nThe primary objective of this randomized controlled trial (RCT) is to evaluate the efficacy of WET-SP, in reducing the incidence and severity of SITBs in active duty military service members following a psychiatric hospitalization due to suicidal ideation, suicide plans, or a suicide attempt. Secondary objectives are to evaluate a potential mechanism of change (i.e., decreases in thwarted belongingness \\[cf. social disconnectedness\\]) and moderator of outcomes (i.e., arc of narrative \\[cf. linguistical parameters of the written narratives generated during treatment\\]). Participants randomized to WET-SP + TAU will receive five sessions of WET-SP delivered by the study team during their psychiatric hospitalization plus treatment-as-usual (TAU). Participants randomized to TAU will receive daily contact and patient-centered care delivered by the acute psychiatric inpatient unit provider team (e.g., psychiatrists, therapists, case managers). TAU includes psychiatric assessment, initial stabilization, nurse case management, medication management, treatment of medical comorbidities, group and individual therapy, and discharge planning. Outcome assessments will be administered at pretreatment, posttreatment, and 10-, 20-, and 30-week follow-ups.",[26,27],"Suicide, Attempted","Suicide Threat",[29,14,30,31],"Self-injurious thoughts and behaviors (SITBs)","Military service members","Treatment as usual (TAU)","RECRUITING","2026-05-27",{"date":35,"type":36},"2026-05-29","ACTUAL",{"date":38,"type":36},"2024-08-20",{"date":40,"type":20},"2027-09",{"name":42,"class":43},"Boston University","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":52,"sex":16,"minAge":53,"maxAge":54,"enrollmentInfo":55,"targetDuration":4,"studyType":21,"phases":57,"briefSummary":58,"conditions":59,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":72},"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":56,"type":20},306,[23],"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.",[60,61,62,27],"Suicide Attempts","Suicidal Ideation","Suicide and Self-harm","2025-11-13",{"date":65,"type":36},"2025-11-14",{"date":67,"type":36},"2022-08-11",{"date":69,"type":20},"2027-01-31",{"name":71,"class":43},"Seattle Children's Hospital",2,{"id":74,"slug":75,"hasResults":11,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":79,"eligibilityCriteria":80,"healthyVolunteers":11,"sex":16,"minAge":81,"maxAge":54,"enrollmentInfo":82,"targetDuration":4,"studyType":21,"phases":84,"briefSummary":85,"conditions":86,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":88,"lastUpdatePostDateStruct":89,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":44},"100552730","intensive-crisis-intervention-100552730","NCT06476886","Intensive Crisis Intervention","Intensive Crisis Intervention (ICI) for Adolescent Suicidal Behavior","ICI","Inclusion Criteria:\n\n1. Youth between the ages of 12 years 0 months and 17 years 6 months at time of consent\n2. Present to the Nationwide Children's Hospital (NCH) Psychiatric Crisis Department (PCD) or NCH Psychiatry Consult Liaison (CL) Service with suicidal ideation and\u002For behavior as the primary referral\n3. Be eligible for admission to both YCSU and APIU based on PCD or CL clinician's clinical judgement\n4. Patient and legal guardian must be willing to be admitted to either YCSU or APIU\n5. Youth obtains a score of ≥23 on the Concise Health Risk Tracking Self-Report (CHRT-SR)\n6. Youth resides with a primary caretaker who has legal authority to consent for participation in research\n7. Legal guardian must attend the PCD or CL evaluation\n\nExclusion Criteria:\n\n1. Participants who are unable to understand study procedures (e.g., intellectual disability, actively psychotic)\n2. Inability to speak or read English adequately to understand and complete study consent and procedures\n\nYCSU clinicians, PCD staff, and NCH-BH leaders will be invited to participate based on their roles in the system-of-care.","12 Years",{"count":83,"type":20},213,[23],"The study's purpose is to improve the clinical management of severe crises experienced by youth with psychiatric disorders by examining a brief, evidence-based alternative to inpatient psychiatric care.",[87,61,26,62,27],"Suicide","2025-08-04",{"date":90,"type":36},"2025-08-07",{"date":92,"type":36},"2024-06-03",{"date":94,"type":20},"2026-07-31",{"name":96,"class":43},"Jennifer Hughes",{"id":98,"slug":99,"hasResults":11,"nctId":100,"briefTitle":101,"officialTitle":102,"acronym":4,"eligibilityCriteria":103,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":104,"enrollmentInfo":105,"targetDuration":4,"studyType":21,"phases":107,"briefSummary":108,"conditions":109,"keywords":115,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":120,"lastUpdatePostDateStruct":121,"startDateStruct":123,"completionDateStruct":124,"leadSponsor":126,"locationsCount":72},"100551920","psychoeducational-course-for-suicide-prevention-100551920","NCT06466356","Psychoeducational Course for Suicide Prevention","Psychoeducational Course for Suicide Prevention - a Randomized Controlled Trial","Inclusion Criteria:\n\n* Patients with a suicide attempt, suicidal behavior, or risk of suicidal behavior and a clinician evaluating that the patient has an intention to die\n* Patients with a suicide attempt or suicidal behavior defined as \"a self-inflicted, potentially injurious behavior with a non-fatal outcome for which there is evidence of intention of death and\u002For considered to have had or been close to a suicidal crisis syndrome.\n\nExclusion Criteria:\n\n* Not being sufficiently fluent in Norwegian to provide informed consent, valid responses on psychometric testing or to benefit from a psychoeducative course.\n* A known diagnosis of ICD-10 F 60.3 (borderline personality disorder) with similar symptoms at previous admittances.\n* Ongoing psychosis.\n* A substance abuse condition to such a degree that they are unable to comply with the protocol and are considered to be at risk when attending psychoeducational courses.\n* Organic brain disorders or mental disabilities in such a degree that they are unable to comply with the protocol.\n* Not being able to give an informed consent","99 Years",{"count":106,"type":20},80,[23],"The plan is to include patients with a history of increased risk of suicide. In the aftermath of an episode of imminent suicide risk, patients will receive a psychoeducational course that entails information on different aspects of suicide-related topics, identifying triggers and detecting early warning signals for increased suicide risk. The course culminates in working on completing a individual safety plan to prevent an future increase in suicide risk. The course will incorporate both patients and their next of kin. The psychoeducational course will be compared to a control group where the patients receive one individual session with focus on a safety plan to evaluate the intervention. Both groups will receive treatment as usual (TAU) during both the acute phase and follow-up. The study will be conducted as a randomized controlled trial.",[110,27,111,112,113,114],"Suicide Prevention","Self Efficacy","Stress, Psychological","Psychiatric Emergency","Psychiatric Disorder",[116,117,118,119],"Psychoeducation","Safety plan","Gatekeeper","Suicidal crisis syndrome","2025-02-25",{"date":122,"type":36},"2025-02-26",{"date":92,"type":36},{"date":125,"type":20},"2031-12-31",{"name":127,"class":43},"St. Olavs Hospital"]