[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"recovery-outcomes\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:recovery-outcomes":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,50,81,111,146],{"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":31,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100648355","developing-pilot-postoperative-guidelines-for-improved-functional-outcomes-after-high-risk-cancer-surgery-100648355",false,"NCT07720089","Developing Pilot Postoperative Guidelines for Improved Functional Outcomes After High-Risk Cancer Surgery","Development and Implementation of Pilot Postoperative Guidelines to Improve Functional Outcomes Following High-Risk Surgery for Cancer: A North American Prospective Feasibility Study","Inclusion Criteria:\n\n* Surgeons who perform abdominal surgery for cancer at the study institution\n\nExclusion Criteria:\n\n* Surgeons who do not perform abdominal surgery for cancer\n* Surgeons who are external to the study institution","ALL","18 Years",{"count":19,"type":20},66,"ESTIMATED","INTERVENTIONAL",[23],"NA","The objective of this study is to develop and evaluate the implementation of novel timeline-specific National Comprehensive Cancer Network (NCCN)-style clinical guidelines designed to improve functional outcomes after high-risk abdominal surgery for cancer.",[26,27,28,29,30],"Cancer","Abdominal Cancer Surgery","Surgery","Recovery Outcomes","Functional Outcomes",[32,33,34,35,36],"cancer","abdominal cancer surgery","surgery","recovery outcomes","functional outcomes","NOT_YET_RECRUITING","2026-07-31",{"date":40,"type":41},"2026-08-03","ACTUAL",{"date":43,"type":20},"2026-07",{"date":45,"type":20},"2027-08",{"name":47,"class":48},"University of Alabama at Birmingham","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":56,"eligibilityCriteria":57,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":58,"targetDuration":4,"studyType":21,"phases":60,"briefSummary":61,"conditions":62,"keywords":65,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":49},"100648652","understanding-pathways-to-wellness-and-recovery-in-detroit---digital-recovery-support-services-100648652","NCT07724275","Understanding Pathways to Wellness and Recovery in Detroit - Digital Recovery Support Services","UPWARD Study RCT of Digital Recovery Support Services (D-RSS) Among a Black Population in Recovery From Alcohol Use Disorders","UPWARD D-RSS","Inclusion Criteria:\n\n1. Able to communicate in English and read at an 8th grade reading level.\n2. Able to read and sign an informed consent form.\n3. Comfortable with smartphone technology or willing and able to learn.\n4. Identify as Black or African American.\n5. Is an adult over the age of 18.\n6. Is in recovery from alcohol problems for at least 3 months and no more than 5 years.\n7. Is receiving in-person recovery support services at our partner recovery community center at the time of screening and enrollment.\n8. Willing to receive and respond to weekly texts with a survey link for brief assessments, and complete two in-person research assessments (baseline and 13-week).\n\nExclusion Criteria:\n\nDoes not meet inclusion criteria",{"count":59,"type":20},65,[23],"The goal of this clinical trial is to learn if digital recovery support services (such as smartphone app) help to support alcohol recovery. We focus on a community of Black and African American people with alcohol use disorder (AUD) who receive in-person recovery support services from a recovery community center.\n\nParticipants will:\n\n* Have an initial 2-hour in-person visit with the research team. During this visit, participants will be asked about themselves and their recovery from alcohol problems. They will also learn about digital recovery resources.\n* Use digital recovery resources on their own for 12 weeks.\n* Complete a short, weekly survey about their experience using digital recovery resources.\n* Have a follow-up 1-hour in-person visit where the researcher asks about again about the participants, their recovery and how they felt about using the digital recovery support services.",[63,29,64],"Alcohol Use Disorder","Digital Health",[66,67,68,69,70],"alcohol use disorder","recovery","digital recovery support services","Black population","African American population","RECRUITING","2026-07-20",{"date":74,"type":41},"2026-07-24",{"date":76,"type":41},"2026-06-13",{"date":78,"type":20},"2027-05",{"name":80,"class":48},"Brandeis University",{"id":82,"slug":83,"hasResults":11,"nctId":84,"briefTitle":85,"officialTitle":85,"acronym":86,"eligibilityCriteria":87,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":88,"targetDuration":4,"studyType":90,"phases":4,"briefSummary":91,"conditions":92,"keywords":97,"overallStatus":71,"whyStopped":4,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":103,"completionDateStruct":105,"leadSponsor":107,"locationsCount":110},"100632214","up-study---decipher-persistent-critical-illness-through-in-deep-clinical-phenotyping-100632214","NCT07510776","UP STUDY - Decipher Persistent Critical Illness Through in Deep Clinical Phenotyping.","UPSt_UCI","Inclusion Criteria:\n\n* Adult patients aged 18 years or older;\n* ICU length of stay equal to or greater than 5 days.\n\nExclusion Criteria:\n\n* Patients with an ICU stay \\\u003C 5 days;\n* Patients discharged from the ICU early due to lack of ward availability, rather than clinical recovery;\n* Patients who do not survive the early phase of critical illness (i.e., early ICU deaths).",{"count":89,"type":20},7000,"OBSERVATIONAL","Persistent Critical Illness (PCI) is a condition that affects some patients who remain in the Intensive Care Unit (ICU) for a long time, usually more than 10-14 days. It is estimated to occur in 5-20% of critically ill patients. A recent Portuguese study found that more than 14% of ICU patients stayed longer than 14 days. PCI is often associated with ongoing need for life support, such as mechanical ventilation or medications to maintain blood pressure. However, patients may also experience severe muscle weakness, repeated infections, or other complications, which makes this group very diverse.\n\nOne of the main risk factors for prolonged ICU stay is sepsis, a severe infection that affects the whole body. Other factors-such as prior health conditions, use of corticosteroids, sedation practices, early versus late mobilization, fluid and antibiotic management, and delirium treatment-may also influence the development and course of PCI.\n\nThis study aims to identify different clinical patterns (\"clusters\") among critically ill patients who remain in the ICU for more than 10 days. Patients will be followed until hospital discharge, and up to one year if data are available. Understanding these different patterns will help develop more personalized and effective care strategies for each patient profile.\n\nThe study is a multicenter retrospective cohort including adult patients (≥18 years) admitted to participating ICUs for more than 5 days between 2021 and 2023. Data collected will include demographic, clinical, and laboratory information, details of organ support (such as mechanical ventilation or vasopressors), medications, nutrition, and rehabilitation practices.\n\nStatistical and machine learning methods will be used to identify groups of patients with similar clinical trajectories and to assess how these groups are related to outcomes such as survival, recovery of organ function, or long-term disability.\n\nExpected results are the identification of distinct clinical clusters of PCI that combine clinical and laboratory data, and the development of tailored management strategies to improve recovery and outcomes for patients with PCI.",[93,29,94,95,96],"Critical Illness","Critical Care, Intensive Care","Critical Care","Critical Care Medicine",[98,99,93],"Persistant Critical Illness","Critical care","2026-04-08",{"date":102,"type":41},"2026-04-13",{"date":104,"type":41},"2025-01-13",{"date":106,"type":20},"2027-12-31",{"name":108,"class":109},"Lisbon Academic Medical Center - Centro Académico de Medicina de Lisboa","NETWORK",7,{"id":112,"slug":113,"hasResults":11,"nctId":114,"briefTitle":115,"officialTitle":116,"acronym":117,"eligibilityCriteria":118,"healthyVolunteers":11,"sex":16,"minAge":119,"maxAge":120,"enrollmentInfo":121,"targetDuration":4,"studyType":21,"phases":123,"briefSummary":124,"conditions":125,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":137,"lastUpdatePostDateStruct":138,"startDateStruct":140,"completionDateStruct":142,"leadSponsor":144,"locationsCount":49},"100632971","evaluation-of-the-addpro-vocational-reintegration-program-add-pro-eval-100632971","NCT07520617","Evaluation of the ADD'Pro Vocational Reintegration Program (ADD-PRO-EVAL)","Evaluation of the ADD'Pro Program: A Partnership-Based Approach to Support Vocational Reintegration of Patients Receiving Addiction Care (ADD-PRO-EVAL)","ADD-PRO-EVAL","Inclusion Criteria:\n\n* Adult of working age (18 years or older)\n* Diagnosed substance use disorder receiving medical care\n* Unemployed or on sick leave with a vocational reorientation project\n* Motivated to work in the competitive labour market\n* Living in or wishing to work in the Puy-de-Dôme department (63), France\n* Legally authorised to work\n* Capable of providing written informed consent\n* Affiliated with a French social security scheme\n\nExclusion Criteria:\n\n* Medical care provided under a court-ordered treatment obligation\n* Previously included in the ADD'Pro program\n* Residing outside the Puy-de-Dôme with no plan to work in the department\n* Under legal guardianship (tutelle, curatelle, or sauvegarde de justice)\n* Deprived of liberty","16 Years","70 Years",{"count":122,"type":20},100,[23],"The goal of this clinical trial is to evaluate whether an integrated medico-psychosocial vocational support program (ADD'Pro) can improve employment outcomes in adults with substance use disorders receiving care at a specialized addiction day hospital.\n\nThe main question it aims to answer is:\n\n\\- Does participation in the ADD'Pro program increase the rate of competitive employment (at least one day worked in the open labour market) at 6 months compared to standard employment services?\n\nResearchers will compare participants enrolled in the ADD'Pro program to participants referred to conventional employment services (France Travail or Cap Emploi) to see if structured, dual medico-psychosocial support leads to higher rates of vocational reintegration, better employment preparation, improved quality of life, and reduced physiological stress reactivity.\n\nParticipants will:\n\n* Be randomly assigned to either the ADD'Pro program or standard employment services\n* If assigned to ADD'Pro: receive immediate individualised support from a vocational counsellor (CIP) at the CeCler Association, running in parallel with their hospital addiction care, with no fixed end date\n* If assigned to standard care: be referred to conventional employment services with monthly follow-up interviews at the hospital, and the option to join ADD'Pro after 6 months\n* Complete structured interviews and validated questionnaires at inclusion, 3, 6, and 12 months\n* A sub-sample of up to 50 participants will additionally take part in a simulated job interview stress test (adapted TSST) with salivary biomarker collection and heart rate monitoring at inclusion and 6 months",[126,127,128,129,130,29,131,132,133,134,135,136],"Addiction","Addiction Disorders","Substance Use Recovery","Return to Work","Recovery","Substance Use Disorder (SUD)","Employment, Supported","Employment","Substance Related Disorders","Vocational Rehabilitation","Substance Use (Drugs, Alcohol)","2026-04-02",{"date":139,"type":41},"2026-04-09",{"date":141,"type":20},"2026-04",{"date":143,"type":20},"2029-04",{"name":145,"class":48},"University Hospital, Clermont-Ferrand",{"id":147,"slug":148,"hasResults":11,"nctId":149,"briefTitle":150,"officialTitle":150,"acronym":151,"eligibilityCriteria":152,"healthyVolunteers":11,"sex":16,"minAge":153,"maxAge":4,"enrollmentInfo":154,"targetDuration":4,"studyType":21,"phases":156,"briefSummary":158,"conditions":159,"keywords":161,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":165,"lastUpdatePostDateStruct":166,"startDateStruct":168,"completionDateStruct":170,"leadSponsor":172,"locationsCount":174},"100606469","phase-3-improving-survivorship-for-critically-ill-patients-aged-65-and-over-100606469","NCT07175961","Improving Survivorship for Critically Ill Patients Aged 65 and Over","IMPROVE-65","Inclusion Criteria:\n\n* Was admitted to ICU for at least 48 hours\n* is aged 65 years or older at the time of hospital admission\n* Is alive and ready for hospital discharge\n* Is expected to survive for 6 months beyond hospital discharge (e.g. not discharged on palliative care)\n* Has new disability at hospital discharge measured using the global disability scale\n\nExclusion Criteria:\n\n* Is not expected to reside in Australia for 3 months following randomisation.\n* Is not expected to be living at home within 2 weeks of acute hospital discharge (e.g. prolonged inpatient rehabilitation)\n* Is unable to identify a GP or GP clinic and\u002For are unable or unwilling to attend a GP appointment scheduled by the recovery navigator.\n* Has an existing recovery or nurse navigator as part of their routine clinical care to assist with planning their care after hospital discharge","65 Years",{"count":155,"type":20},300,[157],"PHASE3","IMPROVE-65 is a randomised control trial designed specifically for people aged over 65 who have survived critical illness. It aims to support patients and general practitioners by providing timely, personalised information to help them work together to make informed goals and decisions about their care after hospital discharge. The aim of the study is to improve recovery and avoid preventable hospital readmissions.",[93,29,160],"Care Coordination",[162,163,164],"critical illness","recovery coordination","patient reported outcomes","2025-09-16",{"date":167,"type":41},"2025-09-19",{"date":169,"type":20},"2025-11",{"date":171,"type":20},"2028-02",{"name":173,"class":48},"Australian and New Zealand Intensive Care Research Centre",2]