[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"economic-problems\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:economic-problems":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,50],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100563640","recovery-legal-care-clinical-trial-100563640",false,"NCT06618794","Recovery Legal Care Clinical Trial","HVIP-MLP","Inclusion Criteria:\n\n* Treatment for an interpersonal violent injury at the University of Chicago Trauma Center (e.g., gunshot, stab wound, assault)\n* Ages 14+ years\n* Able to provide informed consent (18 years and older) or assent (14-17 years)\n\nInclusion of women and minorities: This research proposal includes women and ethnic minorities. Patient participants will be primarily non-Hispanic Black or Hispanic race and ethnicity. The study expects participants to be proportional to the population-wide estimates for the South Side community. The majority will be low-income with variable functional health literacy. These characteristics are representative of the target population and describe the population most likely to benefit from the proposed study. Youth stakeholder participants will be multi-ethnic and racially diverse.\n\nInclusion of children: This study will include children ages 14-17 years old, based on Illinois state labor laws for child employment, as well as the ages of youth who are primarily treated for penetrating injury at the UCMC trauma center. This age is also a pragmatic cutoff for children providing meaningful input on community and healthcare solutions to violence.\n\nExclusion Criteria:\n\n* Diagnosis of severe mental illness (e.g., psychotic disorder, schizophrenia, suicidality)\n* Treated for a non-interpersonal violent injury type (e.g., car accident)\n* Treated for self-inflicted or accidental injuries\n* Unable to provide informed consent due to mental status\n* Prior receipt of legal services at UCMC within the past year\n* Currently imprisoned or incarcerated\n* Residing at a non-Illinois address\n* Non-English speakers","ALL","14 Years",{"count":19,"type":20},500,"ESTIMATED","INTERVENTIONAL",[23],"NA","Hospital-Based Violence Intervention Programs (HVIPs) affiliated with trauma centers in the US often focus on individual behavior modification for reduction in re-victimization. There is a lack of reproducible evidence that has demonstrated effectiveness, given the exclusion of addressing inequities in the Social and Structural Determinants of Health (SSDOH), often the root causes of violent injury and preventable homicide. The study investigators created a Medical Legal Partnership (MLP) to partner with an existing HVIP. This novel program offers beside legal assistance to address the SSDOH. The purpose of this study is to evaluate the effectiveness of the HVIP-MLP program in improving perceived stress, violence-related outcomes, legal needs, health-related quality of life, and PTSD symptoms.",[26,27,28],"Firearm Injury","Economic Problems","Injury Traumatic",[30,31,32,33,34,35,36],"Firearm injury","Community violence","Medical-Legal Partnership","Structural violence","Civil law attorneys","Health-Harming Legal Needs","Hospital-Based Violence Intervention Program","RECRUITING","2026-06-04",{"date":40,"type":41},"2026-06-08","ACTUAL",{"date":43,"type":41},"2025-02-10",{"date":45,"type":20},"2027-08-31",{"name":47,"class":48},"University of Chicago","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":16,"minAge":57,"maxAge":4,"enrollmentInfo":58,"targetDuration":60,"studyType":61,"phases":4,"briefSummary":62,"conditions":63,"keywords":65,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":49},"100503517","the-arrc-iii-trial-of-advanced-recovery-room-care-arrc-100503517","NCT05836285","The ARRC III Trial of Advanced Recovery Room Care (ARRC).","ARRCIII","Inclusion Criteria:\n\n* Scheduled for elective or unplanned surgery\n* Scheduled to stay in hospital at least one night after surgery\n* 30-day mortality of 0.5% to 8% by the US National Safety and Quality Improvement Program risk score (NSQIP)\n\nExclusion Criteria:\n\n* Undergoing cardiac surgery\n* Scheduled for postoperative Intensive Care Unit management","18 Years",{"count":59,"type":20},3000,"18 Months","OBSERVATIONAL","A postoperative high-acuity model of care (ARRC) has been shown, in a prospective cohort study of approximately 850 patients, to produce a marked improvement in patient and hospital outcomes, and hospital costs, in medium risk patients (Ludbrook G et al., JAMA Surgery 2023).\n\nThe goal of this observational study is to examine the outcomes after non-cardiac surgery of a larger group of medium risk patients receiving different forms of care -ARRC and usual ward care. The main questions it aims to answer are:\n\nwhat are the outcomes for patients and hospital after the different forms of care, who receives benefit from high acuity care, what underlies the improved outcomes seen with high acuity care.",[64,27],"Post-Surgical Complication",[66,67,68,69,70,71],"postoperative complications","safety","health economics","quality of recovery after surgery","surgery","anaesthesia","2024-08-11",{"date":74,"type":41},"2024-08-14",{"date":76,"type":41},"2023-04-18",{"date":78,"type":20},"2025-12",{"name":80,"class":48},"University of Adelaide"]