[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"nurse-based-care-management\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:nurse-based-care-management":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,53,79,116,150],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":52},"100634604","effect-of-nasogastric-tube-care-training-by-simulation-based-and-video-based-methods-on-nurses-confidence-satisfaction-and-practices-100634604",false,"NCT07541846","Effect of Nasogastric Tube Care Training by Simulation-Based and Video-Based Methods on Nurses' Confidence, Satisfaction, and Practices","Effect of Nasogastric Tube Care Training by Simulation-Based and Video-Based Methods on Nurses' Confidence, Satisfaction, and Practices: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Registered nurses working at the Pediatric Hospital or Kirkuk Teaching\n* Hospital in Kirkuk\n* Male or female nurses\n* Age 18 years or older\n* Nurses involved in direct patient care\n* Nurses willing to participate in the study\n* Nurses able to attend the assigned training and complete the study assessments\n\nExclusion Criteria:\n\n* Nurses who do not agree to participate in the study\n* Nurses who are not available during the study period\n* Nurses who are unable to attend the assigned training session\n* Nurses who do not complete the required study assessments\n* Nurses who participated in the pilot study",true,"ALL","18 Years",{"count":20,"type":21},83,"ESTIMATED","INTERVENTIONAL",[24],"NA","This randomized controlled trial will evaluate the effect of simulation-based and video-based training on nurses' confidence, satisfaction, and clinical practice related to nasogastric tube care, compared with a control group receiving routine training or usual practice. Nasogastric tube care is an essential nursing procedure that requires adequate knowledge, practical skills, and confidence to ensure safe and effective patient care. Participants will be randomly assigned to one of three groups: simulation-based training, video-based training, or control. The findings of this study will provide evidence on effective educational methods to improve nurses' performance in nasogastric tube care and support better quality of care.",[27,28,29,30],"Nurse Based Care Management","Nurse Led Interventions","Nurse Training","Nurse Scope, Practice",[32,33,34,35,36,37,38,39],"Nasogastric tube care","Simulation-based training","Video-based training","Nurses","Confidence","Satisfaction","Clinical practice","Randomized controlled trial","NOT_YET_RECRUITING","2026-04-21",{"date":43,"type":44},"2026-04-24","ACTUAL",{"date":46,"type":21},"2026-05-20",{"date":48,"type":21},"2026-11-20",{"name":50,"class":51},"Heyam Adnan Jabbar","OTHER",2,{"id":54,"slug":55,"hasResults":11,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":59,"eligibilityCriteria":60,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":61,"targetDuration":4,"studyType":22,"phases":63,"briefSummary":64,"conditions":65,"keywords":67,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":78},"100615485","immersive-virtual-reality-for-the-management-of-anxiety-among-nurses-100615485","NCT07293221","Immersive Virtual Reality for the Management of Anxiety Among Nurses","Use of Immersive Virtual Reality for the Management of Anxiety Among Nurses : a Randomized Trial","RVI-Nurse","Inclusion Criteria:\n\nNurses who have received appropriate information, agreed to participate, and signed the informed consent form.\n\nNurses working day shifts (06:00-18:00) with a coffee break scheduled from 09:00 to 09:15.\n\nExclusion Criteria:\n\nNurses who have not provided informed consent or cannot comply with the study protocol.\n\nHistory of photosensitive epilepsy or seizures. Unstable vestibular disorders or a severe history of motion sickness preventing the use of immersive VR.\n\nEmployer refusal if participation cannot be organized outside work obligations (participation must remain voluntary and without professional consequences).",{"count":62,"type":21},56,[24],"The nursing profession is recognized as one of the most demanding in the healthcare sector. Constant exposure to illness, suffering, and death, combined with an increasing workload, leads to fatigue, stress, and especially persistent anxiety. This anxiety affects not only the psychological and physical health of nurses but also the quality of care provided. From an organizational perspective, anxiety promotes absenteeism, demotivation, and turnover, creating a vicious cycle of collective exhaustion.\n\nTo relieve their anxiety, an increasing number of healthcare providers are turning to complementary medicine, particularly immersive virtual reality (VR) interventions.\n\nImmersive VR hypnosis has been used for several years as a non-pharmacological approach to anxiety management. It constitutes a relational experience engaging both physiological and psychological mechanisms, allowing the user to improve their experience and reduce or even eliminate anxiety.\n\nRandomized clinical trials conducted in recent years have evaluated the efficacy of immersive VR hypnosis. Some results indicate that it reduces anxiety more significantly than pharmacological treatments in control groups and is at least as effective as other complementary therapies (relaxation, massage, acupuncture, yoga, etc.). However, the strength of these conclusions remains limited due to a substantial risk of methodological bias. Rigorous new studies, with strict control conditions, are required, particularly regarding the efficacy of hypnosis applied to nurses.\n\nSince 2024, the investigators have offered hypnotic VR sessions to nurses at the Clinique du Pont de Chaume to better manage their anxiety. Despite the high satisfaction rate reported in our questionnaires, the investigators now aim to statistically evaluate the efficacy of this intervention. Ultimately, these results could justify a broader investment in this type of equipment, making it available to a larger number of healthcare professionals but only if this complementary intervention demonstrates scientific efficacy.",[66,27],"Anxiety",[66],"RECRUITING","2026-04-01",{"date":71,"type":44},"2026-04-07",{"date":73,"type":44},"2026-03-01",{"date":75,"type":21},"2028-02-01",{"name":77,"class":51},"SCP Anesthésie - Réanimation de la Clinique du Pont de Chaume",1,{"id":80,"slug":81,"hasResults":11,"nctId":82,"briefTitle":83,"officialTitle":84,"acronym":85,"eligibilityCriteria":86,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":87,"targetDuration":4,"studyType":22,"phases":89,"briefSummary":90,"conditions":91,"keywords":98,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":107,"lastUpdatePostDateStruct":108,"startDateStruct":110,"completionDateStruct":112,"leadSponsor":114,"locationsCount":4},"100588663","reduction-of-complications-associated-with-picc-management-100588663","NCT06944327","Reduction of Complications Associated With PICC Management","Reduction of Complications Associated With PICC Management. Randomization in Care.","PICC managemen","Inclusion Criteria:\n\n* be over 18 years of age\n* accept participation in the study\n* independent patient in the care and management of activities of daily living\n\nExclusion Criteria:\n\n* patient over 18 years of age\n* patient with functional or cognitive limitation\n* patient with mild, moderate or high level of dependence\n* patient does not accept to perform the study\n* patient with device withdrawal prior to 14 days of duration",{"count":88,"type":21},460,[24],"The present study aims to analyze different care routes of the peripheral access central venous catheter to assess which alternative allows a moderate reduction in the level of complications associated with prolonged care frequency, due to the reduction of device manipulation.\n\nA high level of patient satisfaction is detected due to the controlled follow-up of the device care, as well as a decrease in the need for transfer to a center for follow-up.\n\nObjective: Identify the type of care frequency for PIVCs most beneficial for the reduction of complications associated with extraluminal device care (thrombosis, phlebitis, accidental removal, obstruction).",[92,93,94,95,96,97,27],"Treatment Outcome","Vascular Access","Vascular Access Device","Vascular Access Complication","Care Delivery","Nurse",[99,100,101,102,103,104,105,106],"vascular","vascular access","catheter","central catheter","nurse","vascular access device","management","complication","2025-04-23",{"date":109,"type":44},"2025-04-25",{"date":111,"type":21},"2025-10-01",{"date":113,"type":21},"2027-12-31",{"name":115,"class":51},"Fundacion Miguel Servet",{"id":117,"slug":118,"hasResults":11,"nctId":119,"briefTitle":120,"officialTitle":121,"acronym":122,"eligibilityCriteria":123,"healthyVolunteers":11,"sex":17,"minAge":124,"maxAge":4,"enrollmentInfo":125,"targetDuration":4,"studyType":22,"phases":127,"briefSummary":128,"conditions":129,"keywords":135,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":142,"lastUpdatePostDateStruct":143,"startDateStruct":145,"completionDateStruct":147,"leadSponsor":149,"locationsCount":78},"100588234","novel-medical-device-for-pharmacological-therapy-100588234","NCT06938750","Novel Medical Device for Pharmacological Therapy","A Pilot Study of a Novel Medical Device for Pharmacological Therapy: The SecHold Device","Sechold","Inclusion Criteria:\n\n* patients admitted to the intensive care unit\n* patients with authorization to take part in the study\n\nExclusion Criteria:\n\n* Patients with pre-existing medical conditions: Patients with diseases affecting coagulation, such as hemophilia or thrombocytopathies, could be excluded.\n* Active infection patients: Any patient with vascular access site infections or systemic infections may be excluded to avoid complications.\n* Inability to give informed consent: Patients who are unable to understand or consent to participate in the study.","1 Year",{"count":126,"type":21},262,[24],"Background: Different co-creation methods were used to design and prototype a new fixative device for multiple intravenous therapies with the ability to control and identify the pharmacological therapy administered to a patient. Objectives: To validate a newly created device for the reduction of complications related to the use of intravenous therapy Methods: A multidisciplinary team composed of eight professionals specializing in the field of critical care and an engineering professional in industrial design was responsible for collecting, evaluating, and materializing the ideas and needs arising from clinical practice in a device that met the standards of the same.",[93,95,130,131,132,133,97,27,134],"Vascular Access Complications","Catheter Malfunction","Catheter Infection","Therapeutic Drug Management","Innovative Procedures",[136,137,138,139,140,141],"VASCULAR ACCESS","CATHETER","THERAPY","COMPLICATION","DEVICE","CENTRAL VASCULAR ACCESS","2025-04-14",{"date":144,"type":44},"2025-04-22",{"date":146,"type":44},"2023-01-20",{"date":148,"type":21},"2026-09-20",{"name":115,"class":51},{"id":151,"slug":152,"hasResults":11,"nctId":153,"briefTitle":154,"officialTitle":155,"acronym":4,"eligibilityCriteria":156,"healthyVolunteers":16,"sex":17,"minAge":157,"maxAge":4,"enrollmentInfo":158,"targetDuration":4,"studyType":22,"phases":160,"briefSummary":161,"conditions":162,"keywords":163,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":167,"lastUpdatePostDateStruct":168,"startDateStruct":170,"completionDateStruct":172,"leadSponsor":174,"locationsCount":78},"100567194","how-nurses-use-and-evaluate-the-ampoule-peel-device-comparing-manually-opened-vs-device-opened-ampoules-100567194","NCT06665009","How Nurses Use and Evaluate the Ampoule Peel Device: Comparing Manually Opened Vs. Device-Opened Ampoules","Utilization and Evaluation of Ampoule Peel Device","Inclusion Criteria:\n\n* 16 nursing staff members from W72, W75, and the Department of Anesthesiology, who passed the preliminary tests and are willing to continue to the subsequent phases\n\nExclusion Criteria:\n\n* Nursing staff unwilling to participate, unable to manually break ampoules, experiencing difficulty during the preparatory phase, or deciding to discontinue or withdraw during the process.","20 Years",{"count":159,"type":21},16,[24],"Nurses frequently handle ampoule bottles in their daily work, and due to the fragile nature of these glass bottles, manual opening often leads to hand injuries. According to studies, a high proportion of occupational injuries among nurses are caused by handling ampoule bottles, especially hand lacerations. These injuries not only affect work efficiency but also increase medical risks. Therefore, to improve safety and reduce occupational injuries, this study aims to evaluate a patented ampoule peeling device, which has also won the National Innovation Award, to assess whether it can enhance the safety and satisfaction of nurses during their work.",[27],[164,165,166],"ampoule","ampoule peeling device","Device-Opened Ampoules","2024-12-04",{"date":169,"type":44},"2024-12-09",{"date":171,"type":44},"2024-11-29",{"date":173,"type":21},"2025-10-31",{"name":175,"class":51},"Chih-Cheng Wu"]