[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Nablus University for Vocational and Technical Education\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":73},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,43],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100645602","resilience-building-intervention-for-emergency-nurses-in-palestinian-hospitals-100645602",false,"NCT07703319","RESILIENCE-BUILDING INTERVENTION for EMERGENCY NURSES IN PALESTINIAN HOSPITALS","The Effect of a Resilience-Building Intervention on Psychological Well-Being and Advanced Life Support Performance Among Emergency Nurses in Palestinian Hospitals: A Quasi-Experimental Study","RBI-ENPH","Inclusion Criteria:\n\nRegistered nurses currently employed in the Emergency Department of the selected Palestinian hospitals.\n\nNurses working full-time Willingness to commit to the 6-week intervention program and complete all simulation-based assessments.\n\nProvided written informed consent to participate in the study.\n\nExclusion Criteria:\n\n* Nurses who have participated in formal resilience or stress management training programs within the past year.\n\nNurses currently receiving medical or psychological treatment for diagnosed mental health conditions.\n\nNurses with physical or medical conditions that prohibit them from performing Advanced Life Support (ALS) chest compressions during the simulation assessment.",true,"ALL","23 Years","60 Years",{"count":22,"type":23},140,"ESTIMATED","INTERVENTIONAL",[26],"NA","The goal of this quasi-experimental clinical trial is to evaluate the effect of a culturally adapted, six-week resilience-building programme on psychological well-being and clinical performance in emergency nurses working in Palestinian hospitals. The main questions it aims to answer are:\n\nDoes the six-week resilience-building programme improve the psychological well-being of emergency nurses? Does the intervention enhance their Advanced Life Support (ALS) performance during a simulation-based assessment? Researchers will compare the intervention group receiving the resilience-building programme to a non-equivalent control group to see if the intervention leads to significant improvements in adaptive coping, mental health, and simulated clinical performance.\n\nParticipants will:\n\nParticipate in a six-week resilience-building programme integrating cognitive-behavioural techniques, mindfulness, stress inoculation training, and mental rehearsal (intervention group only).\n\nComplete validated questionnaires to measure psychological well-being and resilience before and after the study period.\n\nComplete a standardized, high-fidelity simulated scenario to assess their Advanced Life Support (ALS) clinical performance.",[29],"Resilience, Psychological","NOT_YET_RECRUITING","2026-07-15",{"date":33,"type":34},"2026-07-17","ACTUAL",{"date":36,"type":23},"2026-07",{"date":38,"type":23},"2026-10",{"name":40,"class":41},"Nablus University for Vocational and Technical Education","OTHER",1,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":49,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":51,"minAge":52,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":24,"phases":55,"briefSummary":56,"conditions":57,"keywords":61,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":4},"100613526","using-virtual-reality-technology-on-depression-anxiety-and-stress-among-palestinian-patients-undergoing-breast-biopsy-100613526","NCT07267741","Using Virtual Reality Technology on Depression, Anxiety, and Stress Among Palestinian Patients Undergoing Breast Biopsy","The Impact of Using Virtual Reality Technology on Depression, Anxiety, and Stress Among Palestinian Patients Undergoing Breast Biopsy: Randomized Controlled Trial","VR\u002FRCT","Inclusion Criteria:\n\n* Female patients scheduled to undergo a breast biopsy.\n* Patients older than 18 years.\n* Patients who are able to provide informed consent.\n* Patients with no prior history of severe psychiatric disorders that could affect the assessment of depression, anxiety, or stress.\n* Patients who are willing and able to participate in the VR intervention and complete self-report questionnaires.\n\nExclusion Criteria:\n\n* Patients who have a history of severe psychiatric disorders, epilepsy, hypertension, or chronic pain.\n* Patients who are mute and cannot read or write, patients with visual, hearing, or cognitive impairment.\n* Patients who have implanted hearing aids or cardiac pacemakers.\n* Patients who will receive any anxiolytic, sedative, or hypnotic drugs before or during the procedure.\n* Patients who may be exposed to complications during the procedure.","FEMALE","18 Years",{"count":54,"type":23},80,[26],"The goal of this randomized controlled trial was to investigate the impact of Virtual Reality (VR) technology on depression, anxiety, and stress levels among Palestinian patients undergoing breast biopsy. The study aimed to evaluate the effectiveness of VR as a non-pharmacological intervention to reduce psychological distress associated with the biopsy procedure.\n\nThe main research hypotheses are:\n\nH01: There will be no significant difference in depression levels between patients who receive immersive VR during breast biopsy and those who receive standard care.\n\nH02: There will be no significant difference in anxiety levels between patients who receive immersive VR during breast biopsy and those who receive standard care.\n\nH03: There will be no significant difference in stress levels between patients who receive immersive VR during breast biopsy and those who receive standard care.\n\nParticipants will:\n\nReceive either a VR intervention or standard care during their breast biopsy. Wear a VR headset for 15-30 minutes, experiencing a calming virtual environment designed to promote relaxation.\n\nComplete assessments of depression, anxiety, and stress before and after the procedure using validated psychological questionnaires.",[58,59,60],"Depression","Anxiety","Stress",[62,58,59,60,63,64],"Virtual Reality Technology","Breast Biopsy","Palestinian Patients","2025-11-25",{"date":67,"type":34},"2025-12-05",{"date":69,"type":23},"2025-12-10",{"date":71,"type":23},"2026-02-10",{"name":40,"class":41},""]