[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100570876":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":25,"centralContacts":29,"locations":38,"responsibleParty":59,"collaborators":61,"id":65,"slug":66,"hasResults":67,"nctId":68,"briefTitle":69,"officialTitle":70,"acronym":71,"eligibilityCriteria":72,"healthyVolunteers":67,"sex":73,"minAge":74,"maxAge":75,"enrollmentInfo":76,"targetDuration":18,"studyType":79,"phases":80,"briefSummary":82,"conditions":83,"keywords":86,"overallStatus":41,"whyStopped":18,"lastUpdateSubmitDate":90,"lastUpdatePostDateStruct":91,"startDateStruct":94,"completionDateStruct":96,"leadSponsor":98,"locationsCount":99},{"fullName":5,"class":6},"Tulane University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Intervention Condition","EXPERIMENTAL","The experimental arm condition consists of motivational interviewing with case management and firearm safety training with a licensed clinical social worker (LCSW). Motivational Interviewing (MI) is a participant-centered yet directive method for enhancing readiness to change. The purpose of MI is to help an individual articulate their own reasons and develop their own plans for making behavioral change. MI respects these values of self-determination and self-efficacy, and emphasizes the participant's right to make decisions about change. The firearm safety training (FST) will be led by the team's LCSW and include a brief demonstration, identification of reasons why the participant may or may not practice safe storage, and develop a plan moving forward. The FST will integrate MI techniques throughout the session.",[13],"Behavioral: Motivational Interviewing and Firearm Safety Training, with Case Management",{"label":15,"type":16,"description":17,"interventionNames":18},"Treatment as Usual","NO_INTERVENTION","Patients assigned to the TAU condition will receive standard care for victims of violence at the Trauma Center. All TAU-assigned patients will be screened by psychiatry consult\u002Fliaison staff for posttraumatic symptoms, depression, and substance use. Patients with significant symptoms will be offered pharmacotherapy and\u002For supportive psychotherapy. Patients will also be provided with a list of community resources available for victims of violence, including mental health and social services.\n\nPatients in TAU will receive the same information sheet (e.g., job training) provided to patients in the MI condition.",null,[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":18},"BEHAVIORAL","Motivational Interviewing and Firearm Safety Training, with Case Management","The basic principles of MI as applied to violence risk reduction in victims of gun violence are as follows: Express Empathy, Develop Discrepancy, Roll with Resistance, and Support Self-Determination\u002FSelf- Efficacy. MI practitioners offer themselves as a \"consultant\" while respecting the participant as the real \"expert\" in their own life. MI also affirms the patient's ability to make changes and communicates trust in the patient's judgments about readiness and plans for change. Motivational interviewing sessions will occur once a month, for six months with a licensed clinical social worker (LCSW).\n\nThe LCSW will additionally provide case management over the course of the six month study, and a one time firearm safety training that covers safe storage methods. At the end of the firearm safety training, the participant will be offered a biometric lock box for free.",[9],[26],{"name":27,"affiliation":5,"role":28},"Julia M Fleckman, PhD, MPH","PRINCIPAL_INVESTIGATOR",[30,35],{"name":31,"role":32,"phone":33,"phoneExt":18,"email":34},"Julia M Fleckman, PHD, MPH","CONTACT","504-988-9937","jfleckma@tulane.edu",{"name":36,"role":32,"phone":18,"phoneExt":18,"email":37},"Timothy K Craft, MSW","tcraft@tulane.edu",[39],{"facility":40,"status":41,"city":42,"state":43,"zip":44,"country":45,"countryCode":46,"cosmosGeoPoint":47,"geoPoint":52,"contacts":53},"Tulane School of Public Health and Tropical Medicine","RECRUITING","New Orleans","Louisiana","70112","United States","US",{"type":48,"coordinates":49},"Point",[50,51],-90.07507,29.95465,{"lat":51,"lon":50},[54,57],{"name":55,"role":32,"phone":18,"phoneExt":18,"email":56},"Lexie M Contreras, MPH","lornelas@tulane.edu",{"name":58,"role":28,"phone":18,"phoneExt":18,"email":18},"Julia M Fleckman, PhD",{"type":60,"investigatorFullName":18,"investigatorTitle":18,"investigatorAffiliation":18,"oldNameTitle":18,"oldOrganization":18},"SPONSOR",[62],{"name":63,"class":64},"Centers for Disease Control and Prevention","FED","100570876","supportive-hospital-based-intervention-for-firearm-trauma-100570876",false,"NCT06712940","Supportive Hospital-Based Intervention for Firearm Trauma","Preventing Youth Firearm Violence in New Orleans: A Hospital-Initiated Community Integrated Approach","SHIFT","Inclusion Criteria:\n\n* 16 to 24 years old\n* gunshot wound, stab wound, or assault related blunt force trauma injury treated at University Medical Center\n* reside in the state of Louisiana\n* capacity to provide voluntary informed consent or assent as approved by the Institutional Review Board of Tulane University\n\nExclusion Criteria:\n\n* not voluntarily agreeing to participate\n* not available to participate in study activities in a private room\n* age under 16 or over 24\n* do not reside in the state of Louisiana\n* not acknowledging English as their first language\n* being in the judgment of the trauma surgery service as too physically compromised to participate\n* intellectual disability as estimated by clinician judgment following mental status examination\n* current psychosis as evidenced by structured clinical interview and mental status examination that are administered on as needed basis\n* current legal detention status\n* injury was a result of intimate partner violence\n* does not have the capacity to provide voluntary informed consent or assent as approved by the Institutional Review Board of Tulane University","ALL","16 Years","24 Years",{"count":77,"type":78},350,"ESTIMATED","INTERVENTIONAL",[81],"NA","This study is a quasi-experimental design, specifically a non-randomized controlled trial (NCT) designed to test the effects of gun violence reduction intervention including MI for youth ages 16-24 years old who present to the Emergency Department or ICU Spirit of Charity Trauma Center (SCTC) at University Medical Centers or another area hospital in New Orleans, Louisiana following a gunshot injury or stab wound. The study will utilize an enrollment strategy that involves alternating, across recruitment days, the assigned study condition. Thus, Day 1 participants would be enrolled into TAU, Day 2 participants would be enrolled in MI-case management condition, Day 3 participants would be enrolled in TAU, etc. This proposed design will minimize any confounds associated with self-selection while possibly increasing enrollment rate.\n\nResearch questions include:\n\n1. Will youth allocated to the MI prevention condition have safer firearm related behaviors and beliefs compared to the TAU control condition at 6 months post- enrollment?\n2. Will youth allocated to the MI prevention condition have reduced gun violence recidivism compared to the TAU control condition at 18 months post-enrollment.\n3. How do youth's social and normative environments influence their gun behaviors and attitudes?\n\nResearchers will compare intervention and TAU arms to see if there are any differences in outcome measures.\n\nParticipants will:\n\n1. complete study eligibility assessment, be assigned to one of two conditions depending on the date of assessment, consent, and enroll in the Emergency Department (ED) or inpatient unit of hospital by a study team member,\n2. participate in one of two conditions: MI administered by a licensed clinical social worker, or treatment as usual control group (TAU) administered by a study team member (n=170 per condition)\n3. complete three surveys (baseline, 3-month, and 6-month) conducted by a study team member\n4. 18-month post examination of participant hospital records\n5. have the option to complete a 1-1.5 hour interview, 1-3 months after the 6-month survey is completed (n=50)",[84,85],"Gun Violence Prevention","Adolescent Behavior",[87,88,89],"Firearm","Violence prevention","Youth","2025-02-13",{"date":92,"type":93},"2025-02-17","ACTUAL",{"date":95,"type":93},"2022-08-31",{"date":97,"type":78},"2028-03-30",{"name":5,"class":6},1]