[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"interprofessional-team-collaboration\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:interprofessional-team-collaboration":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,47],{"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":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100642849","development-of-a-pain-rehabilitation-program-for-chronic-pain-after-sci-100642849",false,"NCT07634796","Development of a Pain Rehabilitation Program for Chronic Pain After SCI","Feasibility of a New Digital Pain Rehabilitation Program for People With SCI","Inclusion Criteria:\n\n* two years since injury\n* Stable pain medication?\n\nExclusion Criteria:\n\n* severe cognitive impairment\n* Alcohol or drug abuse\n* does not understand Swedish","ALL","18 Years",{"count":19,"type":20},32,"ESTIMATED","INTERVENTIONAL",[23],"NA","Pain rehabilitation programs are essential for optimal treatment of chronic pain and are usually based on the biopsychosocial model. This is, however, not standard care for people with chronic pain after a spinal cord injury (SCI) due to a biomedical focused perspective of SCI and lack of adapted programs.\n\nThe aims of this feasibility study:\n\n1. Develop a new digital pain rehabilitation program, adapted for the needs of people living with an SCI.\n2. To investigate the feasibility and acceptability of a new digital pain rehabilitation program.",[26,27,28,29,30],"Spinal Cord Injuries","Chronic Pain","Neuropathic Pain","Interprofessional Team Collaboration","Pain Management",[32,33],"participatory design","feasibility study","NOT_YET_RECRUITING","2026-06-02",{"date":37,"type":38},"2026-06-09","ACTUAL",{"date":40,"type":20},"2026-10-01",{"date":42,"type":20},"2027-09",{"name":44,"class":45},"Umeå University","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":57,"phases":4,"briefSummary":58,"conditions":59,"keywords":64,"overallStatus":78,"whyStopped":4,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":82,"completionDateStruct":84,"leadSponsor":86,"locationsCount":46},"100589917","dosage-of-early-rehabilitation-of-icu-patients-100589917","NCT06960642","Dosage of Early Rehabilitation of ICU Patients","Early Rehabilitation of Intensive Care Unit Patients - a Multinational Prospective Observational Study on Dosage and Outcome","ERUPT","Inclusion Criteria:\n\n* Adults (≥ 18 years old) within 48 hours of ICU admission\n* Expected to stay \\> 24 hours in the ICU\n\nExclusion Criteria:\n\n* Patients who receive end-of-life care at the time of screening\n* Patients whose treatment plans are still under discussion and\u002For not all team members are committed to full active treatment\n* Patients whose functional status is unlikely to be obtainable\n* Patients with language barriers",{"count":56,"type":20},6000,"OBSERVATIONAL","Rehabilitation already begins in the intensive care unit (ICU) to maintain or restore the functional capacity of ICU patients and to counteract the long-term effects of intensive care treatment. Mobilisation is an important component.\n\nThe aim of this multinational observational study is to record and evaluate the different mobilisation practices for ICU patients worldwide. The investigators want to find out which forms of mobilisation in intensive care patients achieve the best results in terms of physical function, functional status and quality of life.\n\nThe goal is to recruit over 6,000 patients internationally. No interventions will be carried out, only routine clinical data will be documented and standardised and already established physical tests and questionnaires will be used.",[60,61,62,63,29],"Critical Care, Intensive Care","Critical Illness","Physiotherapy","Early Ambulation",[65,66,67,68,69,70,71,72,73,74,75,76,77],"early ambulation","early rehabilitation","early mobilisation","physiotherapy","Physical Therapy","ICUAW","PICS","Intensive Care Unit Acquired Weakness","Post Intensive Care Syndrom","Physical Function","Critical Care","Interprofessional","Nursing","RECRUITING","2026-02-18",{"date":81,"type":38},"2026-02-20",{"date":83,"type":38},"2025-12-14",{"date":85,"type":20},"2027-06",{"name":87,"class":45},"Medical University of Vienna"]