[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"vital-signs-monitoring\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:vital-signs-monitoring":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,48,76,117],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":4},"100572913","hospital-based-continuous-patient-monitoring-system-100572913",false,"NCT06739447","Hospital Based Continuous Patient Monitoring System","Implementing a Hospital-based Continuous Patient Monitoring System Using Consumer Wearable Devices in Ghana","Inclusion Criteria:\n\n* Pediatric patients presenting with traumatic injury\n* Pediatric patients postoperative status after an appendectomy\n\nExclusion Criteria:\n\n* Pediatric patients missing their upper limbs,\n* Pediatric patients who cannot wear a Fitbit on their wrist for known allergies to rubber or those with traumatic or medical conditions that prevent them from being able to comfortably wear a Fitbit on either hand","ALL","3 Years","18 Years",{"count":20,"type":21},250,"ESTIMATED","INTERVENTIONAL",[24],"NA","In Ghana, and many other low and middle income countries in Africa, manual vital signs monitoring is the prevalent mode of vital signs monitoring because continuous bedside monitors are non-functional. This lack of continuous vital signs monitoring may result in missed opportunities to catch physiologic deterioration.\n\nThe investigators propose to develop a dashboard that is based on the Garmin Venu 3, a consumer wearable device that reliably measures heart rate, SPO2, and respiratory rate, as an alternative to bedside monitors in hospitals in Ghana.",[27,28,29,30],"Trauma","Appendectomy","Pediatric ALL","Vital Signs Monitoring",[32,33,34,35],"Garmin Venu 3","pediatric appendectomy","trauma","vital sign monitoring","NOT_YET_RECRUITING","2026-06-30",{"date":39,"type":40},"2026-07-02","ACTUAL",{"date":42,"type":21},"2026-09-01",{"date":44,"type":21},"2030-01-30",{"name":46,"class":47},"University of Alabama at Birmingham","OTHER",{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":52,"acronym":4,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":16,"minAge":18,"maxAge":4,"enrollmentInfo":54,"targetDuration":55,"studyType":56,"phases":4,"briefSummary":57,"conditions":58,"keywords":61,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":75},"100630329","advance-forsee-advanced-video-monitoring-for-early-signaling-of-adverse-events-and-optimal-discharge-planning-100630329","NCT07486258","ADVANCE-FORSEE. ADVANCEd Video Monitoring FOR Early Signaling of Adverse Events and Optimal dischargE Planning.","Inclusion Criteria:\n\n* Patients admitted to the cardiothoracic ward after cardiac surgery\n* Age ≥ 18\n* Willing and able to sign informed consent form\n\nExclusion Criteria:\n\n* Pregnancy\n* Inability to provide written informed consent\n* Mental disability\n* Language barrier",{"count":20,"type":21},"1 Week","OBSERVATIONAL","In this study cameras placed at the bedside will be evaluated for their ability to safely and accurately measure vital signs, such as heart rate and breathing, continuously after heart surgery. Camera-based measurements will be compared with the usual checks that nurses perform several times a day using sensors on the skin or finger clip.\n\nThe goal is to see whether camera monitoring can help notice changes in a patient's condition earlier. Another aim of the study is to find out whether the camera monitoring can predict if a patient's health is improving or worsening.\n\nPatients and healthcare staff will be asked by the investigators about their experience to learn whether this type of monitoring is acceptable in daily care.",[30,59,60],"Complication","Discharge Planning",[62,30,63,64,65],"ADVANCE FORSEE","Video-based Monitoring","Complication Prediction","Discharge Readiness Planning","2026-03-17",{"date":68,"type":40},"2026-03-20",{"date":70,"type":21},"2026-07",{"date":72,"type":21},"2028-07",{"name":74,"class":47},"Catharina Ziekenhuis Eindhoven",1,{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":81,"acronym":4,"eligibilityCriteria":82,"healthyVolunteers":11,"sex":16,"minAge":83,"maxAge":4,"enrollmentInfo":84,"targetDuration":86,"studyType":56,"phases":4,"briefSummary":87,"conditions":88,"keywords":98,"overallStatus":107,"whyStopped":4,"lastUpdateSubmitDate":108,"lastUpdatePostDateStruct":109,"startDateStruct":111,"completionDateStruct":113,"leadSponsor":115,"locationsCount":75},"100617738","smartwatch-accuracy-for-measuring-vitals-and-anxiety-before-disc-surgery-100617738","NCT07322523","Smartwatch Accuracy for Measuring Vitals and Anxiety Before Disc Surgery","Validation of Smartwatch Technology for Preoperative Monitoring of Sleep Quality, Anxiety, and Vital Signs in Patients Undergoing Disc Herniation Surgery","Inclusion Criteria:\n\n* 22 years and older\n* Currently receiving preoperative care\u002Fassessment for disc herniation surgery.\n* No history of any cardiovascular disease other than controlled hypertension.\n* Willingness to wear the smartwatch for a minimum of 8 consecutive hours during the night before surgery.\n* Ability to follow all instructions related to the smartwatch operation and data collection independently.\n* No known allergy to nickel.\n\nExclusion Criteria:\n\n* Patients who are currently receiving prescribed medication specifically for sleep in the clinical setting.\n* Refusal or unwillingness to participate in the study.\n* The participant fails to wear the smartwatch correctly or appropriately as per study instructions, leading to incomplete or unreliable data collection.","22 Years",{"count":85,"type":21},60,"3 Months","This study aims to verify the accuracy of blood pressure, heart rate, blood oxygen saturation, anxiety level, and sleep cycle data measurements obtained from Samsung smartwatches compared to the currently accepted method used in patients with disc herniation undergoing the preoperative period.",[89,90,91,92,93,94,30,95,96,97],"Disc Herniations","Disc Herniation, Lumbar","Cervical Disc Herniation","Preoperative Anxiety Score","Sleep Quality","Preoperative Care","Smart Watch","Wearable Devices","Surgical Nursing",[99,100,101,102,103,104,105,106],"Disc herniations","wearable devices","smart watch","vital signs monitoring","sleep quality","anxiety","surgical nursing,","preoperative","RECRUITING","2025-12-22",{"date":110,"type":40},"2026-01-07",{"date":112,"type":40},"2025-11-01",{"date":114,"type":21},"2026-03-30",{"name":116,"class":47},"Halil Kalaycı",{"id":118,"slug":119,"hasResults":11,"nctId":120,"briefTitle":121,"officialTitle":122,"acronym":123,"eligibilityCriteria":124,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":125,"targetDuration":4,"studyType":22,"phases":127,"briefSummary":128,"conditions":129,"keywords":132,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":138,"lastUpdatePostDateStruct":139,"startDateStruct":141,"completionDateStruct":143,"leadSponsor":145,"locationsCount":75},"100596050","aromatherapy-and-music-on-pain-vital-signs-and-parental-satisfaction-in-children-undergoing-peritoneal-dialysis-100596050","NCT07040410","Aromatherapy and Music on Pain, Vital Signs and Parental Satisfaction in Children Undergoing Peritoneal Dialysis","The Effect of Aromatherapy and Music on Pain, Vital Signs and Parental Satisfaction in Children Undergoing Peritoneal Dialysis Treatment: A Randomized Controlled Study","2024-KAEK-11","Inclusion Criteria:\n\n* Children will be included between the ages of 3 and 18 who receive instrumental peritoneal dialysis or continuous outpatient peritoneal dialysis treatment.\n* Children who have a sufficient cognitive level (3-18 years) to determine pain scores,\n* Children who have a healthy hearing and vision system,\n* Children who did not take painkillers, opioids or sedatives 6 hours before the study,\n* Children who have absence of severe pain in another part of the body,\n* Children who have absence of a history of allergies,\n* Children and parents who can speak and understand Turkish.\n\nExclusion Criteria:\n\n* Decline to participate in the study,\n* Peritonitis diagnosis,\n* Pain due to catheter immobilization,\n* Receiving the first session of peritoneal dialysis treatment",{"count":126,"type":21},45,[24],"This study is an experimental randomized controlled study conducted to compare the effect of two different nonpharmacological treatment methods (aromatherapy and music therapy) on pain, vital signs and parental satisfaction to alleviate or eliminate pain during excretion and filling in children undergoing peritoneal dialysis treatment. The study population consists of pediatric patients aged 3 to 18 years undergoing peritoneal dialysis treatment at Basaksehir Cam and Sakura City Hospital between June 2025- 2026. According to literature, for experimental studies and parametric measurements, at least 30 participants should be included in both experimental and control groups. Therefore, this crossover randomized design will include 45 children per group: control, aromatherapy, and music therapy. Children included in the sample will be assigned to groups based on a crossover randomized design. This method is suitable for studies with a small sample size. Since three different interventions will be applied once per session over three sessions, to avoid bias, the order of interventions will be randomized and labeled as A, B, and C. The researcher will write the names of the interventions on three separate papers, draw them one by one, and assign them accordingly: Method A: Aromatherapy, Method B: Music Therapy, Method C: Control. Then, the six possible sequences (ABC, ACB, BAC, BCA, CAB, CBA) will be written on six papers and drawn randomly to determine the intervention order for each participant.",[130,30,131],"Pain","Parental Satisfaction",[133,134,135,136,137],"peritoneal dialysis treatment","pain management","pain in children","non-pharmacological method","satisfaction","2025-06-26",{"date":140,"type":40},"2025-06-27",{"date":142,"type":21},"2025-06-25",{"date":144,"type":21},"2026-06-25",{"name":146,"class":47},"Istanbul Saglik Bilimleri University"]