[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"pics-f\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:pics-f":32},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,55],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":33,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":43,"lastUpdatePostDateStruct":44,"startDateStruct":47,"completionDateStruct":49,"leadSponsor":51,"locationsCount":54},"100622989","behavioral-health-collaborative-care-model-in-post-icu-clinic-family-pilot-100622989",false,"NCT07390786","Behavioral Health Collaborative Care Model in Post-ICU Clinic Family Pilot","Integration of a Behavioral Health Collaborative Care Model Into an ICU Recovery Clinic-Pilot for Families","Inclusion Criteria:\n\n\\- Family member of ICU Recovery Clinic patient enrolled in parent BH CoCM study\n\nExclusion Criteria:\n\n* Serious mental illness (e.g., schizophrenia, mania)\n* Late-stage dementia or cognitive impairment\n* Limited English proficiency\n* No internet-enabled device\n* Prisoners","ALL","18 Years",{"count":19,"type":20},150,"ESTIMATED","INTERVENTIONAL",[23],"NA","This pilot study evaluates the feasibility and acceptability of implementing a Behavioral Health Collaborative Care Model (BH CoCM) for family members of ICU survivors. The intervention includes telehealth-enabled behavioral health assessments and access to the NeuroFlow platform. A subset of participants will undergo qualitative interviews.",[26,27,28,29,30,31,32],"Critical Illness Recovery","Behavioral Health Concerns","Anxiety","Depression - Major Depressive Disorder","PTSD","Critical Care, Intensive Care","PICS-F",[34,35,36,37,38,39,40,41,30,32],"Critical Ilness","critical care recovery","Post-Intensive Care Syndrome","Post-ICU care","behavioral health","mental health","anxiety","depression","RECRUITING","2026-03-11",{"date":45,"type":46},"2026-03-12","ACTUAL",{"date":48,"type":46},"2026-01-30",{"date":50,"type":20},"2028-06-30",{"name":52,"class":53},"Medical University of South Carolina","OTHER",1,{"id":56,"slug":57,"hasResults":11,"nctId":58,"briefTitle":59,"officialTitle":59,"acronym":60,"eligibilityCriteria":61,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":62,"targetDuration":64,"studyType":65,"phases":4,"briefSummary":66,"conditions":67,"keywords":69,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":85},"100615292","post-intensive-care-syndrome---multicentre-prospective-registry-database-of-the-dach-region-100615292","NCT07290712","Post-Intensive Care Syndrome - Multicentre Prospective Registry Database of the DACH Region","PICS-DACH","Inclusion Criteria:\n\n* Patients with an ICU stay longer than 72 hours will be included\n\nExclusion Criteria:\n\n* Age \\\u003C 18 years old\n* Patients who receive end-of-life care at the time of screening",{"count":63,"type":20},5000,"5 Years","OBSERVATIONAL","Post-Intensive Care Syndrome (PICS) refers to long-term cognitive, physical, and psychological impairments that can arise after intensive care treatment. These symptoms may begin within 24 hours of ICU admission and persist for years. Affected patients and their families (PICS-F) face significant burdens, with up to 94% of relatives impacted. Given its high prevalence and socioeconomic impact, this prospective registry study aims to identify risk factors and long-term consequences of PICS and PICS-F.\n\nThe study consists of six modules, starting with data collection during ICU stays and continuing with follow-ups at various intervals post-discharge (up to five years). The primary goal is to investigate diagnostic and therapeutic strategies, while secondary objectives include identifying risk factors, determining impairment severity, and exploring biological mechanisms. Standardized questionnaires and biological samples (blood) are used for data collection.",[68,32],"PICS",[68,32,70,71,72,73,74,75],"ICU","Intensive Care Unit","Critical Care","Critical Illness","Post Intensive Care Syndrome","Post Intensive Care Syndrome Family","2026-02-17",{"date":78,"type":46},"2026-02-19",{"date":80,"type":46},"2026-02-04",{"date":82,"type":20},"2035-11-01",{"name":84,"class":53},"Medical University of Vienna",4]