[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"photoplethysmography\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:photoplethysmography":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,45,76,107],{"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":4,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100648378","wearable-blood-pressure-monitoring-comparison-study-100648378",false,"NCT07719660","Wearable Blood-Pressure Monitoring Comparison Study","Wearable Blood-Pressure Monitoring Comparison Study (WBPMCS)","WBPMCS","Inclusion Criteria:\n\n* Blood pressure measurements can be performed on at least one arm, for example no amputation, dialysis shunt, or obstructive dressing\n* Ability to understand the study information and provide written informed consent\n* For participants in the intensive care unit: an arterial line placed for clinical reasons\n\nExclusion Criteria:\n\n* Wrist circumference exceeds the size range of the investigated wearable devices\n* Physical or medical conditions preventing placement of the wearable devices, including relevant skin lesions, wounds, severe edema, or patient restraint\n* Inability to provide written informed consent",true,"ALL","21 Years","85 Years",{"count":22,"type":23},120,"ESTIMATED","OBSERVATIONAL","The goal of this clinical trial is to compare the accuracy, clinical applicability, and usability of different wearable blood pressure monitoring methods integrated in wearable devices, such as smartwatches, in hospitalized patients. The study evaluates novel photoplethysmography (PPG)-based and wrist-oscillometric blood pressure measurement methods against established clinical reference methods (upper-arm cuff measurements on the general ward and invasive arterial blood pressure monitoring (A-line) in the intensive care unit).\n\nThe main questions the study aims to answer are:\n\n* Can novel blood pressure monitoring methods suitable for integration into wearable devices achieve clinically acceptable agreement with established reference measurements?\n* How does the performance of calibration-dependent wearable devices change over time following calibration?\n* How does the performance of the investigated methods compare with each other?\n* How do the investigated methods perform for patients with different pre-existing conditions ?\n\nTo answer these questions, participants will undergo:\n\n* blood pressure measurements using different wearable devices based on PPG and wrist oscillometry\n* standardized reference blood pressure measurements using an upper-arm cuff (general ward) or an existing invasive arterial line (intensive care unit)\n* repeated measurements over three consecutive days on the general ward to assess calibration stability and measurement reproducibility,",[27,28,29,30,31],"Hypertension","Blood Pressure Monitoring","Wearable Devices","Photoplethysmography","Cuff","NOT_YET_RECRUITING","2026-07-22",{"date":35,"type":36},"2026-07-23","ACTUAL",{"date":38,"type":23},"2026-07-20",{"date":40,"type":23},"2027-12-31",{"name":42,"class":43},"Technische Universität Dresden","OTHER",2,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":17,"sex":18,"minAge":53,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":24,"phases":4,"briefSummary":56,"conditions":57,"keywords":60,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":4},"100647061","synchronised-ecg-and-ppg-data-collection-for-ai-based-qtqtc-reconstruction-ilecs-ecgppg-100647061","NCT07684807","Synchronised ECG and PPG Data Collection for AI-based QT\u002FQTc Reconstruction (ILECS-ECGPPG)","Collection of Synchronised ECG and PPG Recordings in Healthy Adult Volunteers to Develop and Evaluate AI Methods for ECG- Parameter Reconstruction From PPG (Focus: QT\u002FQTc).","ILECS-ECGPPG","Inclusion Criteria:\n\n* Able to provide written informed consent.\n* Willing and able to comply with all study procedures and attend the required study visits.\n* Age ≥18 years.\n* Able to read or understand Dutch or English.\n\nExclusion Criteria:\n\n* Children\u002Fminors or vulnerable individuals.\n* Skin conditions or allergies preventing safe wear of the CardioWatch or ECG electrodes.\n* Any condition that, in the investigator's opinion, may interfere with study completion or data quality.\n* Compromised circulation, injury, or physical malformation at sensor sites.\n* Known clotting disorders or current prescription anticoagulant therapy.\n* Other health conditions preventing safe participation.\n* Wrist circumference \\\u003C14 cm or \\>23 cm.\n* Any participant who, in the investigator's opinion, does not meet study requirements","18 Years",{"count":55,"type":23},50,"This observational study will collect synchronized photoplethysmography (PPG) and electrocardiogram (ECG) recordings from approximately 50 healthy adult volunteers. Participants will wear the Corsano CardioWatch 297-2 and a reference ECG device simultaneously for approximately 24 hours, including standardized activities and free-lining conditions. The objective is to generate a high-quality paired ECG-PPG dataset to support the development and evaluation of artificial intelligence methods fro reconstructing ECG parameters, with a particular focus on QT\u002FQTc, from PPG signals. The study will also evaluate the feasibility and usability of the wearable monitoring system.",[58,30,59],"Electrocardiography (ECG)","Healthy Volunteers",[61,62,63,64,65],"ECG","PPG","Wearable device","CardioWatch","Digital Health","2026-06-29",{"date":68,"type":36},"2026-07-06",{"date":70,"type":23},"2026-07",{"date":72,"type":23},"2026-10",{"name":74,"class":75},"Corsano Health B.V.","INDUSTRY",{"id":77,"slug":78,"hasResults":11,"nctId":79,"briefTitle":80,"officialTitle":80,"acronym":81,"eligibilityCriteria":82,"healthyVolunteers":11,"sex":18,"minAge":53,"maxAge":4,"enrollmentInfo":83,"targetDuration":85,"studyType":24,"phases":4,"briefSummary":86,"conditions":87,"keywords":90,"overallStatus":95,"whyStopped":4,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":106},"100576520","types-of-photoplethysmographic-waves-in-adult-patients-with-septic-shock-100576520","NCT06786364","Types of Photoplethysmographic Waves in Adult Patients with Septic Shock","SHOCK PLETH","Inclusion Criteria:\n\n* Adult patients of 18 years of age and above dignossed with septic shock according to the definition stated in Sepsis 3.0\n* Patients with axillary temperature above 36°C\n* Patients and\u002For family that agree to participate in such study and sign the informed consentment\n* Patients that tolerate supine position\n\nExclusion Criteria:\n\n* Patients with Cardiogenic shock, hipovolemic, obstructive and distributive (neurogenic, anafilactic) shock the exception being septic shock\n* Patients with history of any type of cardiac arrhythmia\n* Patients with history of chronic hepatic disease\n* Patients with limited or diffuse systemic sclerosis\n* Patients that have scarring, nail polish or thickened nails that may impede the proper placement and accurate measurement of photoplethysmography with the pulse oximeter\n* Patients with history of heart insufficiency P- atients with septic shock that already have vasopressor aggents",{"count":84,"type":23},116,"1 Day","The objective of this study is to identify the types of Photoplethysmographic waves present in adults with septic shock and determine whether these waves correlate with other variables of tissue hypoperfusion such as capillary refil, serum lactate and mottling score.",[88,30,89],"Shock Septic","Waveform",[91,92,93,30,94],"shock septic","waveform","vasodilation","arterial tone","RECRUITING","2025-01-15",{"date":98,"type":36},"2025-01-22",{"date":100,"type":36},"2024-11-01",{"date":102,"type":23},"2025-05-30",{"name":104,"class":105},"Hospital General de México Dr. Eduardo Liceaga","OTHER_GOV",1,{"id":108,"slug":109,"hasResults":11,"nctId":110,"briefTitle":111,"officialTitle":112,"acronym":113,"eligibilityCriteria":114,"healthyVolunteers":11,"sex":18,"minAge":53,"maxAge":4,"enrollmentInfo":115,"targetDuration":4,"studyType":24,"phases":4,"briefSummary":117,"conditions":118,"keywords":120,"overallStatus":95,"whyStopped":4,"lastUpdateSubmitDate":123,"lastUpdatePostDateStruct":124,"startDateStruct":126,"completionDateStruct":128,"leadSponsor":130,"locationsCount":44},"100557325","contactless-assessment-of-patient-vital-signs-for-triage-using-remote-photoplethysmography-in-the-emergency-department-100557325","NCT06536647","Contactless Assessment of Patient Vital Signs for Triage Using Remote Photoplethysmography in the Emergency Department","Contactless Assessment of Patient Vital Signs for Triage Using Remote Photoplethysmography in the Emergency Department - 1 Observational Study (CAPTURE-1 Study)","CAPTURE-1","Inclusion Criteria:\n\n* age \\>\u002F= 18 years\n* a valid written consent\n\nExclusion Criteria:\n\n* age \\\u003C 18 years\n* refusal of consent\u002Fpre-existing mental illness rending consent impossible",{"count":116,"type":23},1200,"Remote photoplethysmography (rPPG) is a camera-based method that enables contactless measurement of variation in light absorbance by haemoglobin as reflected by the changes in skin colour\u002Fpixel intensity unperceivable by human eyes. Beat-to-beat variation of light-absorbance can be used to estimate the change in the arterial blood volume underneath the skin and different vital signs including the blood pressure, heart rate, respiratory rate and oxygen saturation (SpO2) of the patient.\n\nThe investigators propose an observational prospective study to independently evaluate the accuracy of contactless vital sign measurements using a cell phone-based remote photoplethysmography (rPPG) technology. This study will recruit adult patients presenting to the Accident and Emergency Department (A\\&E) of Queen Mary Hospital (QMH) between 1 August 2024 and 30 October 2024. The study will be divided into 2 stages. In the initial run-in period, the investigators will collect facial video data from 200 patients to calibrate the VitalsTM system in the A\\&E environment. Then, the investigators will evaluate the accuracy of the VitalsTM in estimating vital signs of 1,000 ambulatory patients in the A\\&E setting.\n\nA trained research nurse and research assistant will be deployed from 09:00 to 17:00 on weekdays to screen for eligible patients in the A\\&E waiting hall and to recruit patient participants throughout the study period. In this study, the investigators will only recruit triage category 3 (semi-urgent) to 5 (non-urgent) patients who are clinically stable and evaluate the performance of the VitalsTM in a designated room in A\\&E. Written informed consent will be obtained from all patient participants after an explanation of the details of the study, including the rationale, benefits and risks of participation.\n\nAfter informed consent, contactless and manual measurement of patient blood pressure, heart rate, respiratory rate, body temperature and SpO2 will be carried out simultaneously in a designated room in A\\&E. A mounted light emitting diode (LED) will be used as the light source. Facial video of the patient participant will be captured using an iPhone, an iPad and a thermal camera placed at around 50 cm from the patient. A reference object for thermal and visual imaging will be placed at the background. Also, ambient temperature and light intensity will be measured.\n\nThe patient will be asked to sit down and remain still during video-recording. Manual measurement will be performed simultaneously by a trained research nurse or research assistant using standard hospital device or other medical-grade devices. A software program will be used to log vital sign measurements and recordings simultaneously so that data can be synchronised to reduce variations.\n\nThe primary outcome is the accuracy of the VitalsTM platform in estimating patient heart rate measured in intraclass correlation coefficient (ICC). The investigators will also measure of accuracy of the VitalsTM platform in estimating other vital signs, including blood pressure, respiratory rate, SpO2 and body temperature. The investigators will also evaluate patient satisfaction and comfort with the contactless and manual measurement techniques.\n\nThe accuracy of contactless measurement will be determined by calculating the ICC from the manual measurement readings as the ground truths. The investigators will also calculate the root mean square error (RMSE) and Pearson correlation between the contactless and manual measurement readings for individual vital signs. Altman Bland plot will be used to evaluate the bias and limits of agreement between two vital sign measurement methods.",[30,119],"Vital Signs",[30,119,121,122],"Emergency department","Triage","2025-01-14",{"date":125,"type":36},"2025-01-16",{"date":127,"type":36},"2024-09-23",{"date":129,"type":23},"2025-12-31",{"name":131,"class":43},"The University of Hong Kong"]