[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"medical-care\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:medical-care":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,50,80],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":29,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100604336","quality-of-life-and-medical-care-of-long-term-sarcoma-survivors-in-germany-prosa-100604336",false,"NCT07148193","Quality of Life and Medical Care of Long-term Sarcoma Survivors in Germany (PROSa+)","Understanding Long-Term Sarcoma Survivorship: Risk Profiles, Outcomes and Unmet Needs - A Joint Project of Research, Sarcoma Centres and Patient Experts (PROSa+)","PROSa+","Inclusion Criteria:\n\n* Diagnosis of sarcoma according to the International Classification of Diseases for Oncology (ICD-O) and World Health Organization (WHO) classification, including soft tissue sarcoma, bone sarcoma, and GIST\n* At least 5 years since initial sarcoma diagnosis\n* With or without active disease\n* Age ≥18 years at the time of study participation\n\nExclusion Criteria:\n\n* Diagnosis of Desmoid tumors\n* Inability to complete a structured questionnaire (e.g., due to insufficient German language skills, cognitive impairment, dementia)","ALL","18 Years",{"count":20,"type":21},1600,"ESTIMATED","OBSERVATIONAL","The study PROSa+ aims to assess patient-reported outcomes (PROs), patient-reported experiences (PREs), and the socioeconomic situation of long-term sarcoma survivors (≥ 5 years post-diagnosis, with or without active disease) in Germany. The mixed-methods research design includes a multicenter observational study with a cross-sectional questionnaire survey involving 1,600 participants (paper, online), qualitative interviews with up to 60 participants, and longitudinal analyses combining data from existing sarcoma registries and the previous PROSa study conducted between 2017 and 2020.",[25,26,27,28],"Sarcoma","Survivorship","Quality of Life (QOL)","Medical Care",[25,30,31,32,28,33,34,35,36],"Neoplasms","Patient-Reported Outcomes","Patient-Reported Experiences","Quality of Life","Unmet Health Needs","Oncology","Psycho-Oncology","RECRUITING","2025-12-01",{"date":40,"type":41},"2025-12-08","ACTUAL",{"date":43,"type":41},"2025-11-28",{"date":45,"type":21},"2027-09",{"name":47,"class":48},"Technische Universität Dresden","OTHER",5,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":17,"minAge":57,"maxAge":4,"enrollmentInfo":58,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":60,"conditions":61,"keywords":64,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":79},"100568163","evaluation-of-medical-and-social-care-for-elderly-patients-between-hospital-and-home-temporary-accommodation-out-of-hospitalization-by-nursing-home-and-long-term-care-units-in-ile-de-france-region-100568163","NCT06677645","Evaluation of Medical and Social Care for Elderly Patients, Between Hospital and Home: TEMPORARY ACCOMMODATION Out of Hospitalization by Nursing Home and Long-Term Care Units in Ile-de-France Region","HTSH","* Inclusion Criteria:\n\n  1. Patient selection criteria\n\n     * Patient male or female at least 60 years of age, as initially defined with the Regional Health Agency, discharged from hospital,\n     * Oral expression of non opposition to participation in the study, documented in the medical record by the physician,\n     * Presenting a defined and feasible plan for returning home,\n     * Whose social\u002Fmedical situation (stabilized) does not allow an immediate return home after hospitalization.\n  2. Caregiver selection criteria\n\n     * Person with an unpaid caregiving activity for their relative in HTSH,\n     * Person verbally expressing their non-opposition to participating in the study, and documented in the medical record of the patient they are helping,\n     * A person who is able to understand the study questionnaires and evaluations, and is able to answer them without the help of a third party.\n  3. Professional selection criteria\n\n     * Salaried professional, nursing or not, regularly and directly involved in the HTSH circuit, whether in hospital or in nursing home \u002F long term care units, for at least 6 months,\n     * Oral expression of non opposition to participation in the study, documented by the establishment.\n* Non-inclusion Criteria:\n\n  * Be already included in another clinical study,\n  * Benefit from a legal protection measure or be unable to express their consent, in accordance with article L1121-8 of the French Public Health Code.","60 Years",{"count":59,"type":21},258,"Prospective, observational, non-interventional, comparative, multicenter RIPH3 study to investigate the impact of HTSH on length of hospital stay in referring services.",[62,28,63],"Social Care","Elderly Patients",[65,66,67,68,69],"social care","Tempory hospitalization","Elderly people","Medical care","medical-economic study","2025-06-10",{"date":72,"type":41},"2025-06-13",{"date":74,"type":41},"2024-11-20",{"date":76,"type":21},"2027-11-20",{"name":78,"class":48},"Gérond'if",10,{"id":81,"slug":82,"hasResults":11,"nctId":83,"briefTitle":84,"officialTitle":85,"acronym":86,"eligibilityCriteria":87,"healthyVolunteers":11,"sex":17,"minAge":88,"maxAge":89,"enrollmentInfo":90,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":92,"conditions":93,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":102,"lastUpdatePostDateStruct":103,"startDateStruct":105,"completionDateStruct":107,"leadSponsor":109,"locationsCount":111},"100499869","invasive-group-a-streptococcal-infection-100499869","NCT05788861","Invasive Group A Streptococcal Infection","French Pediatric Nationwide Observatory of Invasive Group A Streptococcal Infection (in Childen for 0 to 18 Ages)","ISAI","Inclusion Criteria:\n\n* Age\\\u003C18 years\n* Documented invasive Group A Streptococcus infection (identification of GAS in a normally sterile site or from another site in case of toxin shock or necrotizing dermo-hypodermatitis)\n\nExclusion Criteria:\n\n* Opposition of the patient or his\u002Fher legal representative","1 Day","17 Years",{"count":91,"type":21},100,"This study is observational, retrospective and prospective study in pediatric patients hospitalized with invasive streptococcal A infection",[94,95,96,28,97,98,99,100,101],"Sepsis Due to Streptococcus, Group A","Risk Factors","Severe Infection","Medical Complications","Outcome, Fatal","Therapy","Strain","Virulence Factors","2024-02-07",{"date":104,"type":41},"2024-02-08",{"date":106,"type":41},"2022-09-01",{"date":108,"type":21},"2026-09-01",{"name":110,"class":48},"Association Clinique Thérapeutique Infantile du val de Marne",1]