[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"clinical\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:clinical":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,44,71],{"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":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100386546","virtual-biopsy-development-to-identify-patients-glioma-grade-at-the-chu-of-poitiers-using-magnetic-resonance-imaging-100386546",false,"NCT04313140","Virtual Biopsy Development to Identify Patient's Glioma Grade at the CHU of Poitiers Using Magnetic Resonance Imaging","MR3TGLIOBIOPSY","Inclusion Criteria:\n\n* Age≥ 18 years,\n* Patient with suspected glioma with prior imaging\n* Subject free, with legal protection guardianship or curatorship;\n* Enrollment in the French Social Security system;\n* Informed consent signed by the patient\n\nExclusion Criteria:\n\n* Any contraindication to an MRI examination\n* Legal protection, namely minors, persons deprived of their liberty by a judicial or administrative decision, persons residing in a health or social establishment, adults under legal protection and finally patients in emergency situations\n* Pregnant or lactating women, women of childbearing age who do not have effective contraception","ALL","18 Years",{"count":19,"type":20},500,"ESTIMATED","INTERVENTIONAL",[23],"NA","Glioma is a tumor of the central nervous system. These lesions are sorted with the WHO ranking regarding the tumoral oncotype. The tumoral MRI assessment is the first step before any medical decision. Currently, only anatomical biopsy can give the tumor grade definition and help to define the most adapted treatment.",[26,27,28,29,30],"Development of the Virtual Biopsy","Tumor Grade","Artificial Intelligence Algorithms","Clinical","Radiological","RECRUITING","2026-05-04",{"date":34,"type":35},"2026-05-08","ACTUAL",{"date":37,"type":35},"2021-02-22",{"date":39,"type":20},"2029-02",{"name":41,"class":42},"Poitiers University Hospital","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":52,"sex":16,"minAge":53,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":21,"phases":56,"briefSummary":57,"conditions":58,"keywords":4,"overallStatus":60,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":70},"100636350","ai-based-clinical-orientation-for-nursing-students-100636350","NCT07564544","AI-Based Clinical Orientation for Nursing Students","The Effects of an Artificial Intelligence-Based Clinical Orientation Program on Nursing Students Orientation Process in Pediatric Nursing Practice","ClinicOrient","Inclusion Criteria:\n\n* Being enrolled in the Pediatric Nursing course for the first time.\n* Being a third-year nursing student.\n* Providing voluntary informed consent to participate in the study.\n\nExclusion Criteria:\n\n* Being absent during the course of the study.\n* Currently being employed as a healthcare professional.\n* Having a frozen enrollment status.",true,"19 Years",{"count":55,"type":20},90,[23],"Aim: This experimental study aims to investigate the impact of an Artificial Intelligence (AI)-based orientation program on the clinical orientation process of nursing students during their pediatric nursing clinical practice.Materials and Methods: The study population will consist of 186 third-year nursing students enrolled in the spring semester at a state university. The sample will include 90 students (45 intervention, 45 control) who meet the study criteria and volunteer to participate. Students in the intervention group will receive an AI-based clinical orientation program, while the control group will receive no additional intervention beyond the standard faculty and hospital orientation. Data will be collected between February and March 2026 using a \"Descriptive Information Form,\" the \"Clinical Adaptation Scale for Student Nurses,\" and the \"Therapeutic Communication Skills Scale for Nursing Students\" in a pre-test\u002Fpost-test design.Statistical Analysis: Data will be analyzed using SPSS 25.0. Descriptive statistics (frequency, percentage, mean, and standard deviation) will be used. Normality will be assessed via Kolmogorov-Smirnov\u002FShapiro-Wilk tests. For group comparisons, Chi-square, ANOVA, independent samples t-test, Mann-Whitney U, and Wilcoxon tests will be utilized. The statistical significance level will be set at $p \\\u003C 0.05$.Ethical Considerations: Ethical committee approval and necessary permissions from scale authors will be obtained before the study begins. Informed consent will be collected from all participants after explaining the study objectives.Keywords: Orientation training, nursing, student, artificial intelligence, clinical practice.",[59,29],"Orientation","NOT_YET_RECRUITING","2026-05-03",{"date":63,"type":35},"2026-05-07",{"date":65,"type":20},"2026-04-30",{"date":67,"type":20},"2026-06-11",{"name":69,"class":42},"Selcuk University",2,{"id":72,"slug":73,"hasResults":11,"nctId":74,"briefTitle":75,"officialTitle":75,"acronym":4,"eligibilityCriteria":76,"healthyVolunteers":11,"sex":16,"minAge":77,"maxAge":4,"enrollmentInfo":78,"targetDuration":4,"studyType":80,"phases":4,"briefSummary":81,"conditions":82,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":86,"lastUpdatePostDateStruct":87,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":43},"100570454","postoperative-clinical-and-neurophysiological-assessment-of-patients-after-open-heart-surgery-100570454","NCT06707454","Postoperative Clinical and Neurophysiological Assessment of Patients After Open Heart Surgery","Inclusion Criteria:\n\n* Patient ≥ 60 years.\n* Both sexes.\n* Patients who are scheduled for on-pump open heart surgery either isolated coronary artery bypass grafting (CABG) or combined CABG and valve surgery.\n\nExclusion Criteria:\n\n* Patients with a past history of CNS disease (e.g. Epilepsy, brain tumors, or Dementia).\n* Patients with metabolic disturbance.\n* Illiterate patient.\n* Patient with sever cognitive impairment on Mini-mental state Examination (MMSE) and\u002For Montreal Cognitive Assessment (MoCA)\n* Patients who cannot undergo DEEG recordings (eg, uncooperative).\n* Patients with abnormal brain images except for small vessel disease.","60 Years",{"count":79,"type":20},80,"OBSERVATIONAL","This study aims to investigate postoperative clinical, cognitive and neurophysiological assessment of patients after open heart surgery among sample of Egyptian patients.",[83,29,84,85],"Postoperative","Neurophysiological Assessment","Open Heart Surgery","2024-11-24",{"date":88,"type":35},"2024-11-27",{"date":90,"type":35},"2023-06-01",{"date":92,"type":20},"2025-05-01",{"name":94,"class":42},"Ain Shams University"]