[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT06880809":3,"trial-entities:NCT06880809":112,"trial-summary:NCT06880809":116},{"id":4,"nct_id":4,"org_study_id":5,"brief_title":6,"official_title":7,"overall_status":8,"completion_date":9,"status_verified_date":10,"last_update_date":11,"start_date":12,"sponsor_name":13,"lead_sponsor_class":14,"has_dmc":15,"brief_summary":16,"detailed_description":17,"conditions":18,"keywords":20,"study_type":24,"primary_purpose":25,"phases":26,"enrollment_info":28,"interventions":31,"primary_outcomes":37,"secondary_outcomes":65,"sex":66,"minimum_age":67,"maximum_age":68,"healthy_volunteers":69,"eligibility_criteria":70,"std_ages":82,"locations":84,"central_contacts":101,"overall_officials":108,"references":110,"see_also_links":111},"NCT06880809","CHLA-25-00072","Bridge the Gap (BTG) - Black Youth Group","Bridging the Gap: A Collaborative Intervention Group for Black Youth at Risk for Suicide","RECRUITING","2027-06-01","2026-04","2026-04-30","2025-06-01","Children's Hospital Los Angeles","OTHER",false,"The goal of this clinical trial is to develop and preliminarily test a culturally adapted suicide intervention specifically for black youth. The main question it aims to answer:\n\n-To evaluate the feasibility and acceptability of the group, as well as the preliminary efficacy of the group for decreasing suicidal thoughts and behaviors and increasing protective factors such as hope, positive ethnic identity, and family and peer support.\n\nParticipants will be asked to attend 10-week group intervention and complete pre-treatment and post-treatment assessment measures.",null,[19],"Suicide Prevention",[19,21,22,23],"Black Youth","Collaborative Assessment & Management of Suicidality (CAMS)","Group Intervention","INTERVENTIONAL","PREVENTION",[27],"NA",{"count":29,"type":30},16,"ESTIMATED",[32],{"type":33,"name":6,"description":34,"armGroupLabels":35},"BEHAVIORAL","Participants will complete a group intervention, rooted in the Collaborative Assessment \\& Management of Suicidality (CAMS) evidence-based model, driven by their own unique identification of suicide drivers.",[36],"Treatment Arm",[38,42,46,49,52,55,58,61],{"measure":39,"description":40,"timeFrame":41},"The Collaborative Assessment & Management of Suicidality - Suicide Status Form (SSF)","An assessment of suicide risk that consists of six core assessment constructs: psychological pain, stress, agitation, hopelessness, self-hate, and overall risk of suicide; as well as reasons for living and reasons for dying constructs, and wish to live and wish to die constructs.","From pre-treatment until 3 months post-treatment, approximately 23 weeks.",{"measure":43,"description":44,"timeFrame":45},"Ethnic Identity Scale (EIS)","A 17-item scale that assesses the three components of ethnic identity and distinguishes between exploration, resolution, and affirmation. Scores range from 17-68, with higher scores indicating higher levels of affirmation, exploration, and resolution.","From baseline until 3 months post-treatment, approximately 22 weeks.",{"measure":47,"description":48,"timeFrame":45},"Living Ladder Scale","A one-item measure that is prospectively associated with suicidal ideation and suicide attempts by measuring readiness to continue living among individuals thinking of suicide. Scores range from 0-8, with 8 indicating an individual is committed to making changes to make their lives worth living.",{"measure":50,"description":51,"timeFrame":45},"Brief Suicide Cognitions Scale (B-SCS)","A 6-item self-report scale that measures the suicidal belief system, including dimensions of unlovability, unbearability, and unsolvability. Scores range from 6-30, with lower scores indicating fewer suicide cognitions.",{"measure":53,"description":54,"timeFrame":45},"Therapeutic Relationship Working Alliance Inventory, Short Revised (WAI-SR)","A 12-item scale that reflects Bordin's three-dimensional conceptualization of therapeutic alliance: task, goal, and bond. Scores range from 12-60, with higher scores indicating higher therapeutic alliance.",{"measure":56,"description":57,"timeFrame":45},"Optimism and Hope Scale (OHS)","A 14-item scale that measures an individual's level of both optimism, as characterized by a positive outlook on the future, and hope, as characterized by the belief in one's ability to achieve goals and navigate challenges. Scores range from 14-56, with lower scores indicating more hope and optimism.",{"measure":59,"description":60,"timeFrame":45},"Parent Readiness for Hospital Discharge Scale (RHDS)","A 23-item scale aimed at providing a discharge readiness assessment before pediatric discharge from care in hospital settings. Scores range from 0-80, with higher scores indicating more readiness.",{"measure":62,"description":63,"timeFrame":64},"Group Cohesion Scale","A 12-item self-report scale that measures group cohesion, including dimensions of engagement, conflict, and avoidance. Scores across the subscales range from 0-72; higher scores indicate more of that dimension.","From baseline until the beginning of post-treatment, approximately 10 weeks.",[],"ALL","12 Years","17 Years",true,{"inclusion":71,"exclusion":76,"raw_text":81},[72,73,74,75],"12-17 years old","Identify as Black or African American or being of African descent","Have current suicidal ideation or suicidal ideation within the last 30 days","Have assent from the adolescent participant and consent from an individual's caregiver or guardian to participate.",[77,78,79,80],"An active psychotic disorder or current psychosis symptoms","No history of suicide attempt(s) or suicide ideation in the past 30 days","Cognitive deficits or a medical condition diagnosed from a medical provider that precludes full understanding of study materials as assessed through an inability to complete the pre-treatment CAMS SSF \\& SSP","Caregivers, guardians, and\u002For the patient refuse to participate.","Inclusion Criteria:\n\n* 12-17 years old\n* Identify as Black or African American or being of African descent\n* Have current suicidal ideation or suicidal ideation within the last 30 days\n* Have assent from the adolescent participant and consent from an individual's caregiver or guardian to participate.\n\nExclusion Criteria:\n\n* An active psychotic disorder or current psychosis symptoms\n* No history of suicide attempt(s) or suicide ideation in the past 30 days\n* Cognitive deficits or a medical condition diagnosed from a medical provider that precludes full understanding of study materials as assessed through an inability to complete the pre-treatment CAMS SSF \\& SSP\n* Caregivers, guardians, and\u002For the patient refuse to participate.",[83],"CHILD",[85],{"facility":13,"status":8,"city":86,"state":87,"zip":88,"country":89,"contacts":90,"geoPoint":98},"Los Angeles","California","90027","United States",[91,96],{"name":92,"role":93,"phone":94,"email":95},"Tia Tyndal, Ph.D.","CONTACT","323-361-4648","ttyndal@chla.usc.edu",{"name":92,"role":97},"PRINCIPAL_INVESTIGATOR",{"lat":99,"lon":100},34.05223,-118.24368,[102,104],{"name":103,"role":93,"phone":94,"email":95},"Tia Tyndal, PhD",{"name":105,"role":93,"phone":106,"email":107},"Amy West, PhD","323-361-4478","amwest@chla.usc.edu",[109],{"name":103,"affiliation":13,"role":97},[],[],{"nct_id":4,"conditions":113,"biomarkers":115},[114],"Suicidal Ideation",[],{"nct_id":4,"found":69,"summary":117,"prompt_version":127},{"design":118,"status":119,"heading":120,"summary":121,"follow_up":122,"word_count":123,"commitments":124,"compensation":125,"drugs_mentioned":126},"This is an interventional study, meaning participants will receive a specific treatment. It plans to enroll 16 participants.","completed","Bridge the Gap (BTG) - Black Youth Group for Suicide Prevention","This study, called Bridge the Gap (BTG) - Black Youth Group, is testing a new group program designed to help Black youth who are having thoughts of suicide. The program is based on an existing method called Collaborative Assessment & Management of Suicidality (CAMS) but is adapted to be culturally relevant. Researchers want to see if this group program is practical and well-received, and if it can help reduce suicidal thoughts and behaviors while increasing positive feelings like hope and a strong ethnic identity. You might be able to join if you are 12-17 years old, identify as Black or African American, and have had suicidal thoughts recently. The study plans to enroll 16 participants.","Participants will be followed for approximately 3 months (22-23 weeks) after treatment to measure outcomes.",115,"Participants will attend a 10-week group intervention and complete assessments before and after the treatment.","Not stated in the trial record.",[6],"v2"]