[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Baqiyatallah Medical Sciences University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":78},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,42],{"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":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":4},"100595066","ai-driven-personalization-of-end-of-life-care-for-the-elderly-100595066",false,"NCT07027618","AI-Driven Personalization of End-of-Life Care for the Elderly","\"Evaluating the Effectiveness of an AI-Based Software in Personalizing High-Quality End-of-Life Care for the Elderly: A Randomized Controlled Clinical Trial\"","PEACE-AI","Inclusion Criteria:\n\nAge ≥ 60 years\n\nClinical diagnosis of being in the end-of-life stage, based on criteria such as the Karnofsky Performance Scale or Palliative Performance Scale\n\nInformed consent obtained from the participant or legal representative\n\nAbility to use technology independently or with support provided by the research team\n\nAccess to necessary equipment for the intervention (e.g., wearable sensors, smartphone\u002Ftablet)\n\nExclusion Criteria:\n\nPresence of severe cognitive impairment preventing software use\n\nVoluntary withdrawal from the study at any stage\n\nCritical medical deterioration or death during the study\n\nPoor adherence or insufficient engagement with the intervention software in the intervention group","ALL","60 Years",{"count":20,"type":21},140,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study aims to evaluate the effectiveness of an artificial intelligence (AI)-based software in personalizing high-quality end-of-life care for elderly patients. As the elderly population grows, providing tailored and quality care during the final stages of life becomes increasingly important. This AI software continuously monitors vital signs and behaviors through wearable sensors, offers smart medication reminders, alerts the care team to potential risks, and provides personalized care plans along with psychological and social support.\n\nThe study is designed as a randomized controlled trial comparing two groups: one receiving standard end-of-life care and the other using the AI software. Key outcomes include improving quality of life, reducing adverse events like falls and emergency hospitalizations, increasing patient and family satisfaction, improving medication management, and reducing caregiver burden. Data will be collected over six months to assess these effects. The results will help determine whether AI technology can enhance end-of-life care for seniors and support families and healthcare providers.",[27,28,29],"Artificial Intelligence (AI)","Dementia","Palliative Care","NOT_YET_RECRUITING","2025-06-11",{"date":33,"type":34},"2025-06-18","ACTUAL",{"date":36,"type":21},"2025-07",{"date":38,"type":21},"2026-09",{"name":40,"class":41},"Baqiyatallah Medical Sciences University","OTHER",{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":48,"eligibilityCriteria":49,"healthyVolunteers":50,"sex":17,"minAge":51,"maxAge":52,"enrollmentInfo":53,"targetDuration":4,"studyType":22,"phases":55,"briefSummary":56,"conditions":57,"keywords":65,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":4},"100544500","ideal-skiin-cares-bundle-to-prevent-pressure-injury-100544500","NCT06369688","IDEAL SKIIN CARES Bundle to Prevent Pressure Injury","Effect of IDEAL SKIIN CARES Bundle to Prevent Hospital-acquired Pressure Injury: A Cluster Randomized Clinical Trial","IdealSkinCares","Inclusion Criteria:\n\n* be adults aged 18 years or older;\n* have been hospitalized for a minimum of 48 hours;\n* be willing to participate.\n\nExclusion Criteria:\n\n* patients with significant pre-existing skin conditions or injuries that make it difficult to observe skin integrity;\n* have existing PIs or vascular ulcers upon admission to the hospital (pressure injuries defined by the National Pressure Ulcer Advisory Panel);\n* be at risk of PIs due to limited mobility (requiring physical or mechanical assistance to reposition or move);\n* individuals with urinary or fecal incontinence, mental illness, or severe cognitive impairment upon hospital admission;\n* patients who are hospitalized in day-surgery, critical care, emergency, maternity, pediatrics, mental health and dialysis units;\n* admitted to the hospital for \\>28 days;\n* those with prior experience of PIs or training in PIs care and prevention.",true,"18 Years","90 Years",{"count":54,"type":21},1620,[24],"The study will be a multi-center, triple-blinded, cluster randomized controlled trial (c-RCT) conducted with a three-arm parallel design and a 1:1:1 allocation ratio. The experimental groups will consist of two arms: the intervention group, where patients will receive training in relevant pressure injury care bundles, and the placebo group, where patients will receive training in an irrelevant topic like respiratory care. Both intervention and placebo groups will receive specialized pressure injury prevention (PIP) care bundle from trained wound specialist nurses (WSNs). The third arm will be the control group comprising patients who do not undergo any training course and will receive only routine standard care for PIP care bundle. The aim of c-RCT will be to compare the incidence of hospital-acquired pressure injury (HAPI) in the three study groups and to provide detailed evidence on the effect of the developed pressure injury care bundle, administered by WSNs on the development of HAPI in trained hospitalized patients, as opposed to those receiving routine standard care for PIP care bundle without training.",[58,59,60,61,62,63,64],"Pressure Ulcer","Pressure Injury","Bed Sore","Pressure Sore","Decubitus Sore","Decubitus Ulcer","Skin Ulcer",[59,66,67,68,69],"Care Bundle","Hospital-acquired pressure injury","Randomized Clinical Trial","IDEAL SKIIN CARES","2024-04-15",{"date":72,"type":34},"2024-04-17",{"date":74,"type":21},"2025-10-01",{"date":76,"type":21},"2027-10-01",{"name":40,"class":41},""]