[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100644949":3},{"organization":4,"armGroups":7,"interventions":10,"overallOfficials":10,"centralContacts":15,"locations":21,"responsibleParty":37,"collaborators":10,"id":39,"slug":10,"hasResults":40,"nctId":41,"briefTitle":42,"officialTitle":43,"acronym":10,"eligibilityCriteria":44,"healthyVolunteers":45,"sex":46,"minAge":47,"maxAge":10,"enrollmentInfo":48,"targetDuration":10,"studyType":51,"phases":10,"briefSummary":52,"conditions":53,"keywords":56,"overallStatus":61,"whyStopped":10,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":71},{"fullName":5,"class":6},"Shanghai Zhongshan Hospital","OTHER",[8,12],{"label":9,"type":10,"description":11,"interventionNames":10},"Post-ICU Cognitive Impairment Group",null,"Participants diagnosed with post-ICU cognitive impairment based on DSM-5 criteria, clinical assessment, and corrected MoCA score.",{"label":13,"type":10,"description":14,"interventionNames":10},"Non-Post-ICU Cognitive Impairment Group","Participants without post-ICU cognitive impairment based on DSM-5 criteria, clinical assessment, and corrected MoCA score.",[16],{"name":17,"role":18,"phone":19,"phoneExt":10,"email":20},"Ai rong Zhu, Bachelor's Degree","CONTACT","+86 15160007359","2471015405@qq.com",[22],{"facility":23,"status":10,"city":24,"state":10,"zip":10,"country":25,"cosmosGeoPoint":26,"geoPoint":31,"contacts":32},"Zhongshan hospital, Fudan university","Shanghai","China",{"type":27,"coordinates":28},"Point",[29,30],121.45806,31.22222,{"lat":30,"lon":29},[33],{"name":34,"role":18,"phone":35,"phoneExt":10,"email":36},"Yuxia Zhang, PhD","+86 13816881925","zhang.yuxia@zs-hospital.sh.cn",{"type":38,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100644949",false,"NCT07676864","Eye Tracking for Early Identification of Post-ICU Cognitive Impairment","Early Identification of Post-ICU Cognitive Impairment Using Eye-Tracking Technology: A Prospective Observational Study","Inclusion Criteria:\n\n* Successfully transferred from the ICU to a general ward after ICU treatment.\n* ICU length of stay of at least 24 hours.\n* Conscious and able to cooperate with cognitive assessment and eye-tracking tests.\n* Willing to participate in the study and able to provide written informed consent.\n\nExclusion Criteria:\n\n* Diagnosed with cognitive impairment before ICU admission, such as Alzheimer's disease, based on medical history or previous medical records.\n* Previous diagnosis of mental illness or intellectual developmental disorder.\n* Severe visual, hearing, or eye disease that prevents completion of cognitive assessment or eye-tracking tasks.\n* Severe neurological disease that may affect cognitive function, such as stroke, traumatic brain injury, or intracranial infection.\n* Unable to understand or complete the cognitive assessment or eye-tracking tasks due to severe fatigue, marked inattention, communication disorder, or other reasons as assessed by the research staff.",true,"ALL","18 Years",{"count":49,"type":50},73,"ESTIMATED","OBSERVATIONAL","Some patients may have problems with memory, attention, thinking speed, or other cognitive functions after leaving the intensive care unit (ICU). This is called post-ICU cognitive impairment. Early recognition of this problem may help clinicians provide follow-up care and support more promptly.\n\nThis study will explore whether eye-tracking technology can help identify cognitive impairment in patients soon after ICU discharge. Eye tracking is a non-invasive test that records eye movements while a person looks at images or completes simple visual tasks on a screen. The test does not involve any treatment or change in usual medical care.\n\nParticipants will be adult patients who have been transferred from the ICU to a general ward. Within 7 days after ICU discharge, participants will complete a cognitive assessment and an eye-tracking test. The study team will also collect relevant clinical information from medical records. Patients will be grouped according to whether they have post-ICU cognitive impairment based on cognitive assessment and clinical judgment.\n\nThe main purpose of this study is to assess whether information obtained from eye-tracking tests can help clinicians identify possible post-ICU cognitive impairment at an early stage, when used together with standard cognitive assessment. The study will also compare eye movement patterns between the two groups and explore whether eye-tracking measures add useful information beyond standard cognitive assessment.",[54,55],"Post Intensive Care Syndrome (PICS)","Cognitive Impairment",[57,55,58,59,60],"Eye Tracking","Cognitive Assessment","Intensive Care Unit","Post intensive Care Syndrome","NOT_YET_RECRUITING","2026-06-24",{"date":64,"type":65},"2026-06-30","ACTUAL",{"date":67,"type":50},"2026-08",{"date":69,"type":50},"2027-05",{"name":5,"class":6},1]