[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100652505":3},{"organization":4,"armGroups":7,"interventions":15,"overallOfficials":25,"centralContacts":29,"locations":34,"responsibleParty":78,"collaborators":10,"id":81,"slug":82,"hasResults":83,"nctId":84,"briefTitle":85,"officialTitle":85,"acronym":10,"eligibilityCriteria":86,"healthyVolunteers":83,"sex":87,"minAge":88,"maxAge":10,"enrollmentInfo":89,"targetDuration":10,"studyType":92,"phases":10,"briefSummary":93,"conditions":94,"keywords":96,"overallStatus":37,"whyStopped":10,"lastUpdateSubmitDate":99,"lastUpdatePostDateStruct":100,"startDateStruct":103,"completionDateStruct":105,"leadSponsor":107,"locationsCount":108},{"fullName":5,"class":6},"Mayo Clinic","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Active Adults Undergoing Ambulatory ECG Monitoring",null,"Participants prescribed clinical ambulatory ECG monitoring will wear the Frontier X Plus chest-strap ECG device simultaneously with the MoMe ARC traditional ambulatory ECG monitor during their prescribed monitoring period and typical daily activities, including exercise.",[13,14],"Device: Frontier X Plus chest-strap ECG device","Device: MoMe ARC ambulatory ECG monitor",[16,21],{"type":17,"name":18,"description":19,"armGroupLabels":20,"otherNames":10},"DEVICE","Frontier X Plus chest-strap ECG device","The Frontier X Plus is a chest-strap-based wearable ECG device with embedded dry electrodes and a sensor that captures, stores, analyzes, and transmits ECG data through a mobile application and cloud-based platform for subsequent review.",[9],{"type":17,"name":22,"description":23,"armGroupLabels":24,"otherNames":10},"MoMe ARC ambulatory ECG monitor","The MoMe ARC monitor will be used as the traditional ambulatory ECG comparator and processed according to standard clinical workflows.",[9],[26],{"name":27,"affiliation":5,"role":28},"Elizabeth Dineen, DO","PRINCIPAL_INVESTIGATOR",[30],{"name":27,"role":31,"phone":32,"phoneExt":10,"email":33},"CONTACT","904-953-5230","dineen.elizabeth@mayo.edu",[35,52,64],{"facility":36,"status":37,"city":38,"state":39,"zip":40,"country":41,"countryCode":42,"cosmosGeoPoint":43,"geoPoint":48,"contacts":49},"Mayo Clinic Arizona","RECRUITING","Scottsdale","Arizona","85259","United States","US",{"type":44,"coordinates":45},"Point",[46,47],-111.89903,33.50921,{"lat":47,"lon":46},[50],{"name":51,"role":31,"phone":10,"phoneExt":10,"email":10},"Satyajit Reddy, MD",{"facility":53,"status":37,"city":54,"state":55,"zip":56,"country":41,"countryCode":42,"cosmosGeoPoint":57,"geoPoint":61,"contacts":62},"Mayo Clinic Florida","Jacksonville","Florida","32224",{"type":44,"coordinates":58},[59,60],-81.65565,30.33218,{"lat":60,"lon":59},[63],{"name":27,"role":31,"phone":10,"phoneExt":10,"email":10},{"facility":65,"status":37,"city":66,"state":67,"zip":68,"country":41,"countryCode":42,"cosmosGeoPoint":69,"geoPoint":73,"contacts":74},"Mayo Clinic Rochester","Rochester","Minnesota","55905",{"type":44,"coordinates":70},[71,72],-92.4699,44.02163,{"lat":72,"lon":71},[75],{"name":76,"role":31,"phone":77,"phoneExt":10,"email":10},"Kathryn Larson, MD","507-293-6358",{"type":28,"investigatorFullName":79,"investigatorTitle":80,"investigatorAffiliation":5,"oldNameTitle":10,"oldOrganization":10},"Elizabeth H. Dineen","Principal Investigator","100652505","feasibility-and-usability-of-a-chest-strap-ambulatory-ecg-monitor-in-active-individuals-in-comparison-with-a-traditional-ambulatory-ecg-patch-monitor-mome-arc-100652505",false,"NCT07772817","Feasibility and Usability of a Chest-Strap Ambulatory ECG Monitor in Active Individuals in Comparison With a Traditional Ambulatory ECG Patch Monitor (MoMe ARC)","Inclusion Criteria:\n\n* Adult participants (\\>22 years; Frontier X is approved for use in this age group) who participate in \\>4 days a week of \\>150 minutes total per week of moderate to high intensity exercise who were prescribed a ambulatory ECG monitor for clinical purposes for 24 hours or more.\n* Patients must agree to wear the Frontier X monitor for the prescribed duration and use the Frontier X Plus application\n\nExclusion Criteria:\n\n* Current use of Implanted Cardiac Devices\n* Pregnancy\n* Known allergies to any of the materials listed in the \"List of Patient-Contacting Materials\"\n* Presence of skin injuries or broken skin in the area where the chest strap is worn\n* Inability to use a compatible mobile device required for the operation of the study device\n* Any cognitive or physical limitations that, in the opinion of the investigator, limits the participant's ability to fully follow study procedures\n* Medical restrictions on exercise for safety including cardiac, orthopedic or other relevant past medical history","ALL","22 Years",{"count":90,"type":91},15,"ESTIMATED","OBSERVATIONAL","The purpose of this research is to compare the standard ambulatory ECG monitor, the MoMe ARC, against Fourth Frontier's \"Frontier X Plus\". This device is an FDA-Cleared chest-strap-based ECG wearable that provides an alternative modality to capture ambulatory ECG rhythm changes.",[95],"Cardiac Arrhythmia",[97,98],"Ambulatory electrocardiographic monitoring","Arrhythmia detection","2026-08-14",{"date":101,"type":102},"2026-08-19","ACTUAL",{"date":104,"type":91},"2026-08",{"date":106,"type":91},"2027-06",{"name":5,"class":6},3]