[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"suicide-and-self-harm\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:suicide-and-self-harm":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,9,0,[8,42,67,92,119,145,168,197,219],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100504021","combined-dialectical-behavior-therapy-and-digital-cognitive-behavioral-therapy-for-insomnia-for-adolescents-at-high-risk-for-suicide-100504021",false,"NCT05842863","Combined Dialectical Behavior Therapy and Digital Cognitive Behavioral Therapy for Insomnia for Adolescents at High Risk for Suicide","Combined Dialectical Behavior Therapy and Digital Cognitive Behavioral Therapy for Insomnia for Adolescents at High Risk for Suicide: A Pilot RCT","Inclusion Criteria:\n\n1. 12-18 years of age and not yet graduated from high school.\n2. Insomnia symptoms, defined as a total score of ≥ 8 on the Insomnia Severity Index .\n3. High suicide risk, defined as: \\> 3 lifetime self-harm episodes (with at least 1 in the 12 weeks before baseline screening) and elevated suicidal ideation (≥31 on the SIQ-Jr.).\n4. If taking medication for psychiatric disorders or sleep, must be on a stable dose (\\>2 months).\n5. Youth and parent both speak English.\n6. At least one family member or responsible adult agrees to participate in assessments and in the DBT multi-family skills group.\n7. Youth lives at home.\n\nExclusion Criteria:\n\n1. Significant current mania or psychosis; life threatening anorexia, or other diagnosis of a severe mental or physical condition requiring treatment specific to that disorder and\u002For that interferes with participation in assessments or treatment.\n2. A history of being diagnosed with an Autism Spectrum Disorder.\n3. Has a comorbid untreated sleep apnea or a severe circadian sleep-wake disorder with a habitual bedtime after 3 AM or habitual rise time after 11 AM.\n4. Insomnia symptoms are significantly impacted by substance use or withdrawal of psychoactive medications.\n5. Has conditions that require caution when implementing CBTI, such as bipolar and seizure disorders.\n6. Court-ordered to treatment.",true,"ALL","12 Years","18 Years",{"count":21,"type":22},44,"ESTIMATED","INTERVENTIONAL",[25],"NA","The proposed research addresses the urgent need to reduce suicide rates among teens. This will be the first study that the investigators know of that will examine the feasibility and preliminary effectiveness of augmenting a suicide-focused treatment (Dialectical Behavior Therapy, \\[DBT\\]) with an evidence-based treatment protocol for insomnia (a digital version of Cognitive Behavioral Therapy for Insomnia \\[CBT-I\\]). The goal of this clinical trial is to learn providing insomnia treatment in conjunction with suicide-focused treatment leads to greater reductions in suicidality and self-harm than suicide-focused treatment alone.\n\nParticipants will be randomly assigned to receive 6 months of DBT plus CBT-I or to DBT alone and will complete research assessments measuring suicidal ideation, self-harm behavior and insomnia symptoms every four weeks over the course of the study, as well as one post-treatment follow-up assessment. Participants will also wear a device on their wrist (like a Fitbit or wristwatch) for 10 days following each assessment to collect data about their sleep.",[28],"Suicide and Self-harm","RECRUITING","2026-04-23",{"date":32,"type":33},"2026-04-29","ACTUAL",{"date":35,"type":33},"2024-08-14",{"date":37,"type":22},"2026-06-30",{"name":39,"class":40},"Stanford University","OTHER",1,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":49,"enrollmentInfo":50,"targetDuration":4,"studyType":23,"phases":52,"briefSummary":53,"conditions":54,"keywords":57,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":61,"startDateStruct":62,"completionDateStruct":64,"leadSponsor":66,"locationsCount":41},"100423713","parent-intervention-for-psychiatrically-hospitalized-youth-100423713","NCT04797455","Parent Intervention for Psychiatrically-Hospitalized Youth","Pilot Intervention for Parents of Psychiatrically-Hospitalized Youth","Inclusion criteria are:\n\n* youth is currently hospitalized on the Stanford unit at Mills Peninsula Medical Center, on the Inpatient Adolescent Psychiatry Unit, for suicidal ideation and\u002For a suicide attempt.\n* youth is between the ages of 12-18 (18 year-old youth must still be in high school and living at home with parents for the duration of the study)\n* at least one parent\u002Fguardian is willing to participate in the study intervention\n* youth and parent speak English well enough to complete study treatment and assessments in English\n\nExclusion criteria are:\n\n• the youth or parent has a psychiatric or medical condition that would interfere with their ability to participate in study assessments and\u002For treatment (such as acute psychosis, neurological impairment, malnutrition due to anorexia)","85 Years",{"count":51,"type":22},40,[25],"The purpose of the present study is to conduct a pilot randomized clinical trial (RCT) of a parent coaching intervention for parents of youth hospitalized for suicidal ideation, suicide attempt(s), or non-suicidal self-injury. Parents will receive either the parent coaching intervention (which includes safety planning and behavioral parenting skills training with a clinician and assistance with linkage to follow-up care by a case manager) or treatment as usual (TAU) for the inpatient unit. The long-term goal of the research is to determine if augmenting standard inpatient treatment with additional parenting intervention improves youth treatment response on suicide-related outcomes (i.e., suicidal ideation, non-suicidal self-injury, and suicide attempts). The goal of this pilot RCT is to collect preliminary data needed for a larger RCT, including feasibility, acceptability, safety, tolerability, engagement of the presumed mechanism of change (changes in parent emotions and behaviors), and signal detection of any changes in youth suicide-related outcomes.",[55,28,56],"Adolescent - Emotional Problem","Parenting",[58,59,60],"suicide","Self-Injurious Behavior","Behavioral Symptoms",{"date":32,"type":33},{"date":63,"type":33},"2023-05-01",{"date":65,"type":22},"2026-06-01",{"name":39,"class":40},{"id":68,"slug":69,"hasResults":11,"nctId":70,"briefTitle":71,"officialTitle":72,"acronym":4,"eligibilityCriteria":73,"healthyVolunteers":11,"sex":17,"minAge":19,"maxAge":4,"enrollmentInfo":74,"targetDuration":4,"studyType":23,"phases":76,"briefSummary":77,"conditions":78,"keywords":81,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":86,"completionDateStruct":88,"leadSponsor":90,"locationsCount":41},"100560036","brief-skills-for-safer-living-brief-sfsl-100560036","NCT06571916","Brief Skills for Safer Living (Brief-SfSL)","Investigating the Efficacy of a Novel Therapy for Suicide Risk in Adults: A Randomized Controlled Trial of an Intensive Single Session of \"Brief Skills for Safer Living\"","Inclusion Criteria:\n\n* Suicidal ideation in the past week\n* Access to a computer or phone with a camera\n* Access to internet\n* Access to an emergency contact and hospital within commuting distance\n* Not receiving other psychotherapy\u002Fcounselling services concurrently\n* Willing to have the session recorded to determine therapy fidelity\n* Any psychiatric diagnosis is allowed\n* Follow-up visits with a psychiatrist and\u002For family doctor where a psychotherapeutic modality (e.g., Dialectical Behavioural Therapy, psychodynamic therapy, etc.) is not being used are allowable\n\nExclusion Criteria:\n\n* Inability to undergo psychotherapy in English\n* Presence of cognitive impairment that would limit consent and understanding of Brief Skills for Safer Living\n* Active psychosis\n* Unwilling or unable to provide informed consent\n* Previously enrolled in the Brief-SfSL pilot study\n* Unwilling or unable to communicate verbally",{"count":75,"type":22},150,[25],"The goal of this project is to assess the efficacy of Brief-Skills for Safer Living (Brief-SfSL) in a randomized control trial. The investigators will be testing 150 participants Canada-wide, half of which will be randomized to receive Brief-SfSL (B-TAU) and the other half will be randomized to receive Brief-SfSL after a 3 month waitlist (WL-TAU). The main questions this study seeks to answer are:\n\n* Is B-TAU more efficacious than WL-TAU for reducing suicidal thoughts at 3 months?\n* Is B-TAU more efficacious than WL-TAU at 3 months for reducing depression severity, anxiety, and anhedonia?\n* Is B-TAU more efficacious than WL-TAU at 3 months for improving social connectedness, emotional regulation, functioning (work, life, social), executive control and social problem-solving?\n* Are adverse events equivalent between B-TAU and WL-TAU at 3 months?",[79,80,28],"Suicide Prevention","Suicide",[58,82],"psychotherapy","2026-01-20",{"date":85,"type":33},"2026-01-22",{"date":87,"type":33},"2025-11-17",{"date":89,"type":22},"2028-12-31",{"name":91,"class":40},"Unity Health Toronto",{"id":93,"slug":94,"hasResults":11,"nctId":95,"briefTitle":96,"officialTitle":97,"acronym":4,"eligibilityCriteria":98,"healthyVolunteers":11,"sex":17,"minAge":99,"maxAge":19,"enrollmentInfo":100,"targetDuration":4,"studyType":23,"phases":102,"briefSummary":103,"conditions":104,"keywords":107,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":112,"startDateStruct":113,"completionDateStruct":115,"leadSponsor":117,"locationsCount":41},"100540302","dialectical-behavior-therapy-for-adolescents-with-self-harm-and-suicidal-behavior--an-open-trial-100540302","NCT06315075","Dialectical Behavior Therapy for Adolescents With Self-harm and Suicidal Behavior- an Open Trial","Dialectical Behavior Therapy for Adolescents With Self-harm and Suicidal Behavior- an Open","Inclusion Criteria:\n\n* Age 13-18 years\n* Ongoing or a history of self-harm the last six months; current suicidal behavior (suicidal thoughts or at least one suicide attempt within the previous six months); at least three criteria of Diagnostic and Statistical Manual -5 (DSM-5) Borderline personality disorder (BPD), or the self-destruction criterion of DSM-5 BPD in addition to minimum two subthreshold criteria as assessed by the Structured Clinical Interview for DSM-5 Personality Disorders (SCID-5-PD) (First et al., 2016)\n* Fluency in Norwegian\n* One parent\u002Ftrusted adult that can participate together with the adolescent.\n\nExclusion Criteria:\n\n* Intellectual disability\n* Significant learning or language impairments\n* Autism spectrum disorder\n* Anorexia Nervosa\n* Any psychotic disorder\n* Substance abuse disorder. These patients will be offered treatment as usual at their local outpatient clinic.","13 Years",{"count":101,"type":22},140,[25],"The goal of this pre-post-follow-up study is to examine how well the treatment Dialectical behavior therapy for adolescents (DBT-A) with a duration of 20 weeks for adolescents with self-harm and suicidal behavior works in routine clinical practice. The main questions it aims to answer are:\n\n* to investigate how well DBT-A works after treatment and at 3-month follow-up, measured by episodes of self-harm, suicide attempts, depressive symptoms and quality of life, drop-out from treatment and number of possible participants who decline DBT-A.\n* to investigate how well DBT-A works at 12 months follow-up\n* to investigate whether pre-treatment factors can predict who will benefit from treatment",[105,106,28],"Self-harm","Suicidal Ideation",[28,108,109,110,111],"Adolescents","Dialectical behavior therapy for adolescents","Routine clinical practice","Effectiveness study",{"date":85,"type":33},{"date":114,"type":33},"2024-01-15",{"date":116,"type":22},"2029-12-31",{"name":118,"class":40},"Haukeland University Hospital",{"id":120,"slug":121,"hasResults":11,"nctId":122,"briefTitle":123,"officialTitle":123,"acronym":124,"eligibilityCriteria":125,"healthyVolunteers":16,"sex":17,"minAge":126,"maxAge":127,"enrollmentInfo":128,"targetDuration":4,"studyType":23,"phases":130,"briefSummary":131,"conditions":132,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":135,"lastUpdatePostDateStruct":136,"startDateStruct":138,"completionDateStruct":140,"leadSponsor":142,"locationsCount":144},"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","11 Years","17 Years",{"count":129,"type":22},306,[25],"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.",[133,106,28,134],"Suicide Attempts","Suicide Threat","2025-11-13",{"date":137,"type":33},"2025-11-14",{"date":139,"type":33},"2022-08-11",{"date":141,"type":22},"2027-01-31",{"name":143,"class":40},"Seattle Children's Hospital",2,{"id":146,"slug":147,"hasResults":11,"nctId":148,"briefTitle":149,"officialTitle":150,"acronym":151,"eligibilityCriteria":152,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":127,"enrollmentInfo":153,"targetDuration":4,"studyType":23,"phases":155,"briefSummary":156,"conditions":157,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":159,"lastUpdatePostDateStruct":160,"startDateStruct":162,"completionDateStruct":164,"leadSponsor":166,"locationsCount":41},"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.",{"count":154,"type":22},213,[25],"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.",[80,106,158,28,134],"Suicide, Attempted","2025-08-04",{"date":161,"type":33},"2025-08-07",{"date":163,"type":33},"2024-06-03",{"date":165,"type":22},"2026-07-31",{"name":167,"class":40},"Jennifer Hughes",{"id":169,"slug":170,"hasResults":11,"nctId":171,"briefTitle":172,"officialTitle":172,"acronym":4,"eligibilityCriteria":173,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":174,"targetDuration":4,"studyType":23,"phases":176,"briefSummary":177,"conditions":178,"keywords":184,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":188,"lastUpdatePostDateStruct":189,"startDateStruct":191,"completionDateStruct":193,"leadSponsor":195,"locationsCount":41},"100537143","telehealth-behavioral-activation-for-teens-100537143","NCT06273995","Telehealth Behavioral Activation for Teens","Inclusion Criteria:\n\n1. Participants must be enrolled in the Texas Youth Depression Suicide Research Network (TX-YDSRN) Registry Study;\n2. Be between the ages of 12- 18 or currently enrolled in high school;\n3. Have a caregiver that is willing to participate in the program;\n4. Be able to commit to weekly sessions for eight weeks;\n5. Be currently experiencing depressive symptoms;\n6. Be able to participate in telehealth services within the state of Texas;\n7. Be willing to provide consent\u002Fassent (parents\u002Flegally authorized representative (LAR)\u002Fguardian or young adult participant, aged 18 or older, must be willing to provide consent; youth, aged 12-17, must be willing to provide assent);\n8. Be able to read, write and speak English or Spanish sufficiently to understand the study procedures and provide written informed consent to participate in the study;\n9. Be willing to dedicate appropriate time to complete scheduled study assessment and measures and attend intervention sessions (both parent\u002FLAR\u002Fguardian and youth)\n10. Be able to provide a reliable means of contact.\n\nExclusion Criteria:\n\n1. Have an acute medical or psychological condition(s) that that would, in the judgment of the study medical clinician, make participation difficult or unsafe;\n2. Have an acute medical or psychological condition(s) that would result in an inability to accurately complete study requirements (e.g., neurological conditions or significant neurodevelopmental concerns);\n3. Have active psychotic or manic symptoms resulting in altered mental status and inability to provide assent or requiring immediate attention and\u002For higher level of intervention;\n4. Have a parent\u002FLAR\u002Fguardian who is deemed cognitively unable to provide consent (if youth participant, aged 12-17).",{"count":175,"type":22},250,[25],"Behavioral activation is one such empirically supported intervention. Derived from cognitive-behavioral therapy, a well-established treatment for depression, behavioral activation uses psychoeducation and skill-building to increase an individual's engagement in valued and enjoyable activities (e.g., socializing with family and friends, exercising, participating in a hobby) in order to improve depressive symptoms. Research has shown that behavioral activation is an effective intervention for depressed youth. Additionally, it has been shown as a promising intervention that can be conducted in a brief, virtual format and can be effectively implemented by both trained clinicians and trained, non-licensed interventionists. This project will provide Behavioral Activation for youth (12-17) experiencing depression or suicidal ideation who are currently enrolled in the Youth Depression Suicide Network study in Texas.",[179,28,180,181,182,183],"Depression","Depression in Adolescence","Depression Mild","Depression Moderate","Depression Severe",[185,186,187],"behavioral activation","depression","adolescents","2025-07-18",{"date":190,"type":33},"2025-07-20",{"date":192,"type":33},"2024-03-01",{"date":194,"type":22},"2029-12-01",{"name":196,"class":40},"Baylor College of Medicine",{"id":198,"slug":199,"hasResults":11,"nctId":200,"briefTitle":201,"officialTitle":202,"acronym":4,"eligibilityCriteria":203,"healthyVolunteers":11,"sex":17,"minAge":19,"maxAge":204,"enrollmentInfo":205,"targetDuration":4,"studyType":23,"phases":207,"briefSummary":208,"conditions":209,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":210,"lastUpdatePostDateStruct":211,"startDateStruct":213,"completionDateStruct":215,"leadSponsor":217,"locationsCount":41},"100453116","feasibility-acceptability-and-preliminary-efficacy-of-a-novel-personalized-mobile-intervention-for-suicide---open-trial-2-100453116","NCT05180344","Feasibility, Acceptability, and Preliminary Efficacy of a Novel Personalized Mobile Intervention for Suicide - Open Trial (2)","Feasibility, Acceptability, and Preliminary Efficacy of a Novel Personalized Mobile Intervention for Suicide","Inclusion Criteria:\n\n* Suicidal ideation and\u002For suicidal behavior in the past month verified by the C-SSRS\n* Between the ages of 18 and 26\n* English proficiency\n* Comfortable with smartphone technology\n* Deemed by the treatment team to be stable enough to complete study procedures\n\nExclusion Criteria:\n\n* Current psychotic or manic symptoms severe enough to interfere with study procedures","26 Years",{"count":206,"type":22},10,[25],"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).",[80,28,158,106],"2025-07-14",{"date":212,"type":33},"2025-07-17",{"date":214,"type":33},"2024-07-25",{"date":216,"type":22},"2025-10-01",{"name":218,"class":40},"Butler Hospital",{"id":220,"slug":221,"hasResults":11,"nctId":222,"briefTitle":223,"officialTitle":224,"acronym":4,"eligibilityCriteria":225,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":226,"targetDuration":4,"studyType":23,"phases":228,"briefSummary":229,"conditions":230,"keywords":232,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":236,"lastUpdatePostDateStruct":237,"startDateStruct":239,"completionDateStruct":241,"leadSponsor":243,"locationsCount":144},"100532230","aitbs-for-nssi-and-suicide-in-adolescent-depression-100532230","NCT06210100","aiTBS for NSSI and Suicide in Adolescent Depression","Efficacy and Safety of Accelerated Intermittent Theta Burst Stimulation on Non-suicidal Self-injury and Suicide Behaviors in Adolescents With Unipolar or Bipolar Depression","Inclusion Criteria:\n\n1. Meet the DSM-5 (Diagnostic and Statistical Manual of Mental Disorders 5th Edition) diagnostic criteria for major depressive disorder.\n2. Patients aged 12-18 years with at least one guardian to monitor them for 3 months\n3. HAMD-17 Total score ≥18\n4. Hospitalized patients who had two or more non-suicidal self-injury behaviors meeting the DSM-5 diagnostic criteria in the week before admission (NSSI behavior of more than 5 days in the past year, and a baseline DSHI score ≥2 )\n5. Obtain informed consent from patients and guardians\n\nExclusion Criteria:\n\n1. Substance abusers such as psychoactive drugs or alcohol.\n2. Severe physical disability and unable to complete follow-up.\n3. Comorbid other major mental illnesses that meet the DSM-5 criteria, such as bipolar disorder, schizophrenia, mental retardation, dementia, severe cognitive impairment, attention deficit hyperactivity disorder, etc.\n4. Suffering from any severe physical disease, neurological disease, traumatic brain injury, etc, that affects the structure or function of the brain in the lifetime.\n5. Unable to read, understand and complete the assessment or to cooperate with the investigators.\n6. Any implants covering a pacemaker, metallic or magnetic objects in the body, or other conditions not suitable for rTMS.\n7. A history or family history of epilepsy and other contraindications to TMS.\n8. Daily use of benzodiazepines (more than 2mg\u002Fd), theophylline, stimulants such as methylphenidate, anticonvulsants, etc.\n9. Those who have received systematic psychotherapy (interpersonal relationship therapy, dynamic therapy, cognitive behavioral therapy) or TMS within 3 months before baseline.\n10. Other examination abnormalities considered to be inappropriate by investigators.",{"count":227,"type":22},60,[25],"Repetitive transcranial magnetic stimulation (rTMS) has been successfully used to help patients with treatment resistant depression. However, its role in alleviating self injuries with and without suicidal ideation remained uncertain. This trial will compare the effectiveness of active accelerated intermittent theta burst stimulation (aiTBS) rTMS to a placebo control on non-suicidal self injury (NSSI) and suicidal attempts in patients with major depressive disorder.",[231,106,28],"Non Suicidal Self Injury",[233,234,235],"NSSI","MDD","TMS","2024-08-15",{"date":238,"type":33},"2024-08-16",{"date":240,"type":33},"2024-01-18",{"date":242,"type":22},"2025-02-01",{"name":244,"class":40},"Central South University"]