[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"brief-intervention\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:brief-intervention":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,52,84],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":32,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":46,"leadSponsor":48,"locationsCount":51},"100646254","testing-family-firearm-secure-storage-training-ffast-to-prevent-suicide-100646254",false,"NCT07692854","Testing Family Firearm Secure Storage Training (FFAST) to Prevent Suicide","Improving Secure Storage of Firearms to Reduce Suicide Deaths: A Hybrid Type 1 Implementation Effectiveness Randomized Controlled Trial of the Family Firearms Secure Storage Training (FFAST) Intervention","FFAST RCT","Inclusion Criteria:\n\nVeteran Inclusion Criteria:\n\n1. Enrolled or eligible to be enrolled in the VA healthcare system\n2. enrolled in the Caregiver Program\n3. able to comprehend the informed consent form and provide consent over the phone or via teleconference\n4. firearm owner in which they report at least 1 firearm is currently located in the home and stored in an unsecure manner (e.g., unlocked and\u002For loaded)\n5. an identifiable CSO enrolled in the VA CSP who agrees to participate\n6. willing to participate in the follow-up\n7. technology available to complete the appointment remotely (e.g., computer, tablet, phone)\n\nCSO Inclusion Criteria:\n\n1. CSO of Veteran participant (e.g., spouse, friend, relative)\n2. enrolled in the VA CSP\n3. able to comprehend the informed consent form and provide consent over the phone or via teleconference\n4. willing to participate in the follow-up\n5. willing to assist the Veteran with secure firearm storage\n6. willing to participate in the follow-up\n7. technology available to complete the appointment remotely (e.g., computer, tablet, phone)\n\nExclusion Criteria:\n\nVeteran Exclusion Criteria:\n\n1\\) At imminent risk of suicide or homicide warranting crisis intervention (Veterans can participate once stabilized)\n\nCSO Exclusion Criteria:\n\n1\\) At imminent risk of suicide or homicide warranting crisis intervention (CSOs can participate once stabilized)",true,"ALL","18 Years","80 Years",{"count":22,"type":23},176,"ESTIMATED","INTERVENTIONAL",[26],"NA","Firearms are the lethal means used in over 70% of Veteran suicides with rates of Veteran deaths via self-induced firearm injury rising dramatically (by 64.8%) from 2001 to 2022. Upstream, evidence-based lethal means safety interventions are urgently needed within the VA to address this serious issue. The Family Firearms Secure Storage Training (FFAST) intervention consists of single session in which Veterans and their concerned significant others (CSOs) are guided through a discussion on secure firearm storage practices and develop a safety plan to prepare them for a mental health crisis. This study aims to evaluate the relative effectiveness of FFAST against a control condition in promoting secure firearm storage planning, preparedness for a mental health crisis, and secure storage practices within Veterans and their CSOs. In addition, barriers and facilitating factors of implementing FFAST within the VA Caregiver Support Program and Suicide Prevention 2.0 will be examined to aid in the widespread adoption of FFAST across the VA.",[29,30,31],"Lethal Means Safety","Brief Intervention","Concern Significant Others",[29,33,34,35,36,37,38],"Veterans","Suicide Prevention","Concerned Significant Others","Secure Storage","Firearms","Intervention","NOT_YET_RECRUITING","2026-07-14",{"date":42,"type":43},"2026-07-16","ACTUAL",{"date":45,"type":23},"2026-10-01",{"date":47,"type":23},"2030-09-30",{"name":49,"class":50},"VA Office of Research and Development","FED",1,{"id":53,"slug":54,"hasResults":11,"nctId":55,"briefTitle":56,"officialTitle":56,"acronym":57,"eligibilityCriteria":58,"healthyVolunteers":17,"sex":18,"minAge":59,"maxAge":4,"enrollmentInfo":60,"targetDuration":4,"studyType":24,"phases":62,"briefSummary":63,"conditions":64,"keywords":69,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":76,"startDateStruct":77,"completionDateStruct":79,"leadSponsor":81,"locationsCount":51},"100595983","harm-reduction-intervention-for-anabolic-androgenic-steroids-users-a-randomized-controlled-trial-100595983","NCT07039539","Harm Reduction Intervention for Anabolic-androgenic Steroids Users: a Randomized Controlled Trial","SOS-RCT-HR","Inclusion Criteria:\n\n* Anyone over 15 years of age;\n* Planning to use\u002Fincrease the dose of AAS for aesthetic and\u002For physical performance purposes;\n* Plan to use\u002Fincrease the dose of AAS during eight to twelve weeks.\n\nExclusion Criteria:\n\n* Medical prescription for AAS use;\n* Use for sexual reassignment.","15 Years",{"count":61,"type":23},32,[26],"This clinical trial aims to investigate the short and long-term efficacy of a harm reduction intervention in reducing the use of non-clinical anabolic-androgenic steroids (AAS) in abusive users of AAS. As secondary objectives, the study will investigate the intervention's effect on health parameters (i.e., blood), quality of life, sleep quality, body image, eating behavior, depression, anxiety, fatigue, aggressiveness, cardiovascular parameters, muscle strength, body composition and muscle cross-sectional area outcomes.",[65,66,67,68,30],"Drug Abuse","Harm Reduction","Minimization, Harm","Anabolic Steroids Adverse Events",[70,71,72,73,74,75,30],"human enhancement drug","performance and image enhancement drug","anabolic androgenic steroids","drug consumption","doping","harm reduction",{"date":42,"type":43},{"date":78,"type":23},"2026-08-01",{"date":80,"type":23},"2028-01-30",{"name":82,"class":83},"University of Sao Paulo","OTHER",{"id":85,"slug":86,"hasResults":11,"nctId":87,"briefTitle":88,"officialTitle":89,"acronym":4,"eligibilityCriteria":90,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":91,"enrollmentInfo":92,"targetDuration":4,"studyType":94,"phases":4,"briefSummary":95,"conditions":96,"keywords":4,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":108,"lastUpdatePostDateStruct":109,"startDateStruct":111,"completionDateStruct":113,"leadSponsor":115,"locationsCount":51},"100640122","exploration-of-acceptability-of-alcohol-interventions-100640122","NCT07580378","Exploration of Acceptability of Alcohol Interventions","A Mixed-methods Study Exploring the Acceptability of Psychosocial Interventions and Social Determinants of Engagement With an NHS-led Alcohol Care Service.","Inclusion Criteria:\n\n* Clinical staff who worked in the ELHT alcohol care service, and received training in the delivery of psychosocial interventions using the ITEP Manual, and who are still employed by ELHT in other roles (following de-commissioning of the alcohol care service).\n* Patient data under part 2 of the study, who have not opted to have their data removed, in accordance with the NHS MESH, opt out scheme.\n\nExclusion Criteria:\n\n* Clinical staff who worked in the ELHT alcohol care service, but who no longer work for the trust, or are retired.\n* Clinical staff who did not receive training in the delivery of psychosocial interventions.\n* Any patient data under part 2 of the study, who have opted to have their data removed for use, under the NHS MESH protocols.","67 Years",{"count":93,"type":23},2000,"OBSERVATIONAL","This is a mixed-methods study consisting of a qualitative assessment the acceptability of psychosocial interventions, delivered by clinical staff. The study will also investigate the correlation between demographic variables and engagement with a North West England, NHS-led, alcohol care service, amongst the patient population.",[97,98,99,100,30,101,102,103,104,105,106,107],"Alcohol Misuse","Alcohol Use Disorder","Behaviour Change","Health Behaviour","Outcome Assessment","Social Determinants of Health","Psychosocial Intervention","Socioeconomic Factors","Primary Healthcare","Primary Heath Care","Problem Behavior","2026-05-05",{"date":110,"type":43},"2026-05-12",{"date":112,"type":23},"2026-05-01",{"date":114,"type":23},"2026-06-10",{"name":116,"class":83},"East Lancashire Hospitals NHS Trust"]