[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"physiologic-monitoring\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:physiologic-monitoring":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,41,70,95],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":4},"100649924","detection-of-infant-gastrointestinal-activity-using-sound-technology-100649924",false,"NCT07743216","Detection of Infant GastrointEstinal Activity Using Sound Technology","DIGEST","Inclusion Criteria:\n\n* ≥ 37 weeks Gestational Age (GA)\n\nExclusion Criteria:\n\n* Congenital anomalies\n* Gastrointestinal abnormalities or disorders\n* Low birth weight (\\\u003C 2500 g)\n* Maternal magnesium sulfate exposure prior to delivery\\*\n* Fragile skin or skin conditions precluding sensor placement","ALL","1 Minute","30 Weeks",{"count":20,"type":21},10,"ESTIMATED","OBSERVATIONAL","This pilot study aims to evaluate the feasibility and safety of continuous bowel sound monitoring in healthy term newborn infants using a novel wireless acoustic monitoring system. Participants will undergo a single 4-hour recording during routine postnatal care while bowel sounds are continuously recorded using wearable abdominal sensors. Feasibility will be assessed by participant recruitment and study completion, as well as the acquisition of high-quality, analyzable acoustic data. Bowel sounds will be characterized by assessing the temporal and spectral features of bowel sounds during the early neonatal period and exploring their relationship with routine caregiving activities and feeding.",[25,26,27,28],"Infant, Newborn, Diseases","Bowel Sounds","Physiologic Monitoring","Wearable Sensors","NOT_YET_RECRUITING","2026-07-29",{"date":32,"type":33},"2026-08-03","ACTUAL",{"date":35,"type":21},"2026-09-01",{"date":37,"type":21},"2027-12-01",{"name":39,"class":40},"McGill University Health Centre\u002FResearch Institute of the McGill University Health Centre","OTHER",{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":16,"minAge":48,"maxAge":49,"enrollmentInfo":50,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":52,"conditions":53,"keywords":55,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":64,"startDateStruct":66,"completionDateStruct":67,"leadSponsor":69,"locationsCount":4},"100649755","validation-of-a-wireless-wearable-vital-signs-monitor-in-pediatric-patient-100649755","NCT07739823","Validation of a Wireless Wearable Vital Signs Monitor in Pediatric Patient","Wireless Skin-Adherent Physiologic Sensor Validation in Pediatric Patients - Phase 1 Clinical Study","Inclusion Criteria:\n\n* Neonates (0-28 days of life)\n* Infants (29 days of life - 2 years, i.e., not turned 2 years old)\n* Children (2 years old - 12 years old, i.e., not turned 12 years old)\n\nExclusion Criteria:\n\n* Contraindication to application of skin sensors (e.g., rash, surgical site, skin breakdown, open wounds, burns, active dermatitis, etc.) at the application site.\n* Severe hemodynamic instability requiring escalating interventions.\n* Congenital airway abnormalities interfere with accurate capnography.\n* Diagnosed neuromuscular disorders affecting respiratory mechanics.\n* Known adhesive allergies.\n* Inability to tolerate device placement due to behavioral issues.\n* Participation in conflicting clinical trials.\n* High-frequency oscillatory or mechanical ventilation.\n* Active bronchiolitis with mask intolerance.\n* Recent facial surgery preventing EtCO₂ nasal line placement.\n* Behavioral conditions preventing adherence to device wearing.","0 Days","12 Years",{"count":51,"type":21},42,"This prospective observational study aims to evaluate the accuracy, safety, and feasibility of the ANNE® Chest wireless wearable sensor for continuous monitoring of heart rate, respiratory rate, oxygen saturation, and skin temperature in hospitalized neonates, infants, and children (0 days to 12 years of age) in the neonatal and pediatric intensive care units (NICU and PICU). Measurements obtained from the wireless device will be compared with standard-of-care bedside monitoring and capnography. The study will also assess skin tolerability, signal reliability, and caregiver and healthcare provider perceptions of the device.",[54,27],"Vital Signs Monitoring",[56,57,58,59,60,61,62],"Wireless monitoring","Wearable sensors","Pediatric","Neonate","Infant","Intensive care","Physiologic monitoring","2026-07-28",{"date":65,"type":33},"2026-07-31",{"date":35,"type":21},{"date":68,"type":21},"2027-09-01",{"name":39,"class":40},{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":74,"acronym":4,"eligibilityCriteria":75,"healthyVolunteers":76,"sex":16,"minAge":4,"maxAge":77,"enrollmentInfo":78,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":80,"conditions":81,"keywords":83,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":63,"lastUpdatePostDateStruct":91,"startDateStruct":92,"completionDateStruct":93,"leadSponsor":94,"locationsCount":4},"100649740","miniaturized-vital-sign-monitoring-for-newborns-in-the-delivery-room-100649740","NCT07739810","Miniaturized Vital Sign Monitoring for Newborns in the Delivery Room","Inclusion Criteria:\n\n\\- Infants born by C-Section or vaginal delivery, with ≥35 weeks of gestational age and judged clinically stable immediately after birth.\n\nExclusion Criteria:\n\n* Infants with skin abnormality would potentially increase the risk of injury.\n* Family experiencing too much stress as determined by an attending physician or bedside care team, to not be approached for recruitment.\n* Infants born at \\\u003C35 weeks gestational age.",true,"24 Hours",{"count":79,"type":21},5,"This prospective observational study aims to evaluate the accuracy, safety, and feasibility of the Wireless MicroPremVitals Button Sensor System for continuous monitoring of electrocardiography (ECG), heart rate, respiratory rate, oxygen saturation, and skin temperature in newborn infants in the delivery room. Measurements obtained from the wireless sensor system will be compared with standard-of-care monitoring. The study will also assess skin tolerability, signal quality, and parent and healthcare provider perceptions of the device.",[54,82,27],"Newborn Monitoring",[56,84,85,59,86,87,88,89,90],"Vital signs","Newborn","Delivery room","Wearable sensor","Electrocardiography","Respiratory rate","Skin temperature",{"date":65,"type":33},{"date":35,"type":21},{"date":68,"type":21},{"name":39,"class":40},{"id":96,"slug":97,"hasResults":11,"nctId":98,"briefTitle":99,"officialTitle":100,"acronym":4,"eligibilityCriteria":101,"healthyVolunteers":76,"sex":16,"minAge":102,"maxAge":4,"enrollmentInfo":103,"targetDuration":4,"studyType":105,"phases":106,"briefSummary":108,"conditions":109,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":112,"lastUpdatePostDateStruct":113,"startDateStruct":115,"completionDateStruct":117,"leadSponsor":119,"locationsCount":4},"100645192","non-contact-patient-monitoring-with-millimeter-wave-radar-technology-100645192","NCT07677735","Non-contact Patient Monitoring With Millimeter Wave Radar Technology.","Development of a Contactless Patient Monitoring System Using Millimeter Wave Radar Technology","Inclusion Criteria:\n\n* Participating in the research as a researcher\n\nExclusion Criteria:\n\n* Wanting to withdraw from the research","18 Years",{"count":104,"type":21},6,"INTERVENTIONAL",[107],"NA","This study aims to develop a millimeter wave radar technology-based patient monitoring system that allows for the monitoring of physiological and movement-based data in healthcare settings without requiring physical contact with individuals. The study will involve the creation of hardware and software components for processing, analyzing, and converting signals obtained through radar sensors into clinically meaningful data.",[110,111,27],"Radar","Monitoring","2026-06-25",{"date":114,"type":33},"2026-07-01",{"date":116,"type":21},"2026-08-01",{"date":118,"type":21},"2026-10-01",{"name":120,"class":40},"Rukiye Kokkiz"]