[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"needs-assessment\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:needs-assessment":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,49,76],{"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":21,"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":4},"100623400","baixiaoai-ai-companion-for-cancer-patient-follow-up-100623400",false,"NCT07396142","BaiXiaoAi AI Companion for Cancer Patient Follow-up","Application of BaiXiaoAi Companion AI in the Diagnosis, Treatment, and Follow-up Management of Oncology Patients: A Single-Center, Prospective, Exploratory Study","Inclusion Criteria:\n\n* Adults aged 18 years or older;\n* Patients with a confirmed diagnosis of malignant neoplasms who are currently undergoing treatment or in follow-up, or their primary caregivers;\n* Able to read and communicate in Chinese and independently use WeChat;\n* Willing and able to provide informed consent.\n\nExclusion Criteria:\n\n* Presence of severe psychiatric disorders (e.g., schizophrenia, bipolar disorder) or cognitive impairment (MMSE score \\\u003C 24);\n* Inability to use WeChat or communicate in Chinese;\n* Considered by the investigators to be unsuitable for participation due to psychological or physical conditions.","ALL","18 Years",{"count":19,"type":20},300,"ESTIMATED","6 Months","OBSERVATIONAL","This is a prospective, single-center, exploratory study designed to evaluate the accuracy, user engagement, and user experience of the BaiXiaoAi Companion AI. Upon signing the informed consent form and enrollment, a dedicated \"Doctor-Nurse-Patient-AI\" WeChat group will be established for each participant. Within the group, the BaiXiaoAi AI will provide timely responses based on patient communications and proactively push information regarding disease management and patient education.",[25,26,27,28],"Symptoms and Signs","Artificial Intelligence","Artificial Intelligence Mobile Application","Needs Assessment",[30,31,32,33,34,35,36],"WeChat-based AI companion","Tumor patients,","Cancer patients","Patient satisfaction","Symptom management","Emotional support","Clinical needs assessment","NOT_YET_RECRUITING","2026-02-01",{"date":40,"type":41},"2026-02-09","ACTUAL",{"date":43,"type":20},"2026-01-14",{"date":45,"type":20},"2027-11-30",{"name":47,"class":48},"Cancer Institute and Hospital, Chinese Academy of Medical Sciences","OTHER",{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":56,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":59,"phases":60,"briefSummary":62,"conditions":63,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":4},"100607813","a-pilot-effectiveness-and-implementation-trial-of-csnat-i-in-hong-kong-100607813","NCT07193433","A Pilot Effectiveness and Implementation Trial of CSNAT-I in Hong Kong","Refinement, Pilot Implementation, and Testing of the Carer Support Needs Assessment Tool Intervention (CSNAT-I) in Hong Kong Palliative Care Settings","Inclusion Criteria\n\n* adults ≥18 years old;\n* family members taking a primary role in patient care at home as nominated by the palliative cancer patient;\n* ability to communicate in Chinese.\n\nExclusion Criteria:\n\n* paid caregivers;\n* unable to complete the questionnaire due to mental impairment determined by physicians.",true,{"count":58,"type":20},60,"INTERVENTIONAL",[61],"NA","In this hybrid Type 1 effectiveness-implementation pilot randomized controlled trial, 60 caregivers will be randomized into either the CSNAT-I group or usual care. Preliminary effectiveness outcomes include caregiver burden, distress, and health-related quality of life. Preliminary implementation outcomes include feasibility, fidelity, appropriateness, acceptability, cost of the intervention, as well as barriers and facilitators to intervention implementation. Quantitative data will be analyzed using descriptive analysis and linear mixed effects model, while qualitative data using thematic analysis. The CSNAT-I is expected to be preliminarily effective in improving caregiver outcomes and implementable in Hong Kong palliative care context, which will serve as the foundation for a large trial before integration into daily practice.",[64,65,28,66],"Carers","Palliative Care","Supportive Care","2025-09-18",{"date":69,"type":41},"2025-09-25",{"date":71,"type":20},"2025-09-20",{"date":73,"type":20},"2026-05-20",{"name":75,"class":48},"The Hong Kong Polytechnic University",{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":81,"acronym":82,"eligibilityCriteria":83,"healthyVolunteers":56,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":84,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":86,"conditions":87,"keywords":98,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":118,"lastUpdatePostDateStruct":119,"startDateStruct":121,"completionDateStruct":123,"leadSponsor":125,"locationsCount":127},"100579648","global-survey-on-newborns-hospitalisation-and-parental-experiences---the-hope-study-100579648","NCT06827028","Global Survey on Newborns' HOspitalisation and Parental Experiences - the HOPE Study","Global Survey on Newborns' HOspitalisation and Parental Experiences","HOPE","Inclusion Criteria:\n\nParent or caregiver of a newborn infant born on January 1, 2023, or thereafter, who received\u002Fis receiving special\u002Fintensive care starting within the first week of life such as oxygen therapy or other respiratory support, incubator treatment, intravenous infusions, treatment of (suspected) sepsis, pneumonia, necrotising enterocolitis, malformations, jaundice, nutritional\u002Ffeeding problems, hypoglycemia, etc.\n\nExclusion Criteria:\n\n* Other family members than parents\u002F(primary) caregivers\n* Parents of newborns that did not receive special\u002Fintensive care starting within the first week of life\n* Parents or caregivers of infants born before 1 January 2023\n* Persons with insufficient proficiency of one of the languages of the questionnaire",{"count":85,"type":20},100,"This study aims to explore parents' experiences and emotional burdens related to their newborn's hospital stay using an online survey. Our target population consists of parents of newborns born preterm, with low birthweight, or critically ill. Particularly the presence of infant- and family-centred developmental care (IFCDC) principles as well as support through political framework conditions will be investigated.",[88,89,90,91,28,92,93,94,95,96,97],"Infant, Premature","Infant, Low Birth Weight","Parents","Life Change Events","Anxiety","Fear","Stress, Psychological","Uncertainty","Emotions","Caregiver Burden",[99,100,101,102,103,104,105,106,107,28,108,90,109,110,111,112,113,114,115,116,117],"Parental needs","Infant- and Family-centred developmental care","IFCDC","EFCNI","NICU","Global Parent Survey","Breastfeeding","Breastfeeding support","Politics","HRQoL","Infant, Newborn","Family","Family Support","Family Health","Intensive Care, Neonatal","Patient-Centered Care","Infant Care","Surveys and Questionnaires","Health Care Surveys","2025-04-24",{"date":120,"type":41},"2025-04-27",{"date":122,"type":20},"2025-09-01",{"date":124,"type":20},"2027-12-31",{"name":126,"class":48},"Global Foundation for the Care of Newborn Infants",1]