[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100404640":3},{"organization":4,"armGroups":7,"interventions":13,"overallOfficials":19,"centralContacts":19,"locations":20,"responsibleParty":33,"collaborators":36,"id":40,"slug":41,"hasResults":42,"nctId":43,"briefTitle":44,"officialTitle":44,"acronym":45,"eligibilityCriteria":46,"healthyVolunteers":42,"sex":47,"minAge":48,"maxAge":49,"enrollmentInfo":50,"targetDuration":19,"studyType":53,"phases":54,"briefSummary":56,"conditions":57,"keywords":19,"overallStatus":60,"whyStopped":19,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":69},{"fullName":5,"class":6},"Hopital Neuchatelois","OTHER",[8],{"label":9,"type":6,"description":10,"interventionNames":11},"single arm","single arm study",[12],"Device: Aktiia.product",[14],{"type":15,"name":16,"description":17,"armGroupLabels":18,"otherNames":19},"DEVICE","Aktiia.product","The participants wear Aktiia.bracelet for the duration of the cardiac rehabilitation program. The device is initialized once per week.",[9],null,[21],{"facility":22,"status":19,"city":23,"state":19,"zip":24,"country":25,"countryCode":26,"cosmosGeoPoint":27,"geoPoint":32,"contacts":19},"Réseau Hospitalier Neuchâtelois","Neuchâtel","2000","Switzerland","CH",{"type":28,"coordinates":29},"Point",[30,31],6.931,46.99179,{"lat":31,"lon":30},{"type":34,"investigatorFullName":35,"investigatorTitle":35,"investigatorAffiliation":5,"oldNameTitle":19,"oldOrganization":19},"SPONSOR_INVESTIGATOR","Cyril Pellaton",[37],{"name":38,"class":39},"Aktiia SA","INDUSTRY","100404640","single-center-prospective-study-to-validate-the-performance-of-the-aktiia-optical-blood-pressure-monitoring-obpm-device-at-the-wrist-against-ambulatory-blood-pressure-monitoring-abpm-100404640",false,"NCT04548986","Single-center Prospective Study to Validate the Performance of the Aktiia Optical Blood Pressure Monitoring (OBPM) Device at the Wrist Against Ambulatory Blood Pressure Monitoring (ABPM)","OBPM_ABPM2020","Inclusion Criteria:\n\n* Adult subjects (aged between 21 and 65)\n* Subjects fluent in written and spoken French\n* Subjects enrolled in a 12-weeks cardiac rehabilitation program\n* Subjects agreeing to participate\n* Subjects that have signed the informed consent form\n\nExclusion Criteria:\n\n* Subjects with tachycardia (heart rate at rest \\> 120bpm)\n* Subjects with atrial fibrillation\n* Subjects with severe heart failure (LVEF\\\u003C35%)\n* Subjects with severe renal dysfunctions (eGFR \\\u003C 30mL\u002Fmin\u002F1.73 m2)\n* Subjects with pheochromocytoma\n* Subjects with Raynaud's disease\n* Subjects with trembling and shivering\n* Subjects with interarm systolic difference \\> 15 mmHg\n* Subjects with interarm diastolic difference \\> 10 mmHg\n* Subjects with arm paralysis\n* Women in known pregnancy\n* Subjects with an arteriovenous fistula\n* Subjects with arm amputations\n* Subjects with the upper arm circumference \\> 64 cm\n* Subjects with the wrist circumference \\> 22 cm\n* Subjects with the exfoliative skin diseases\n* Subjects with lymphoedema","ALL","21 Years","65 Years",{"count":51,"type":52},63,"ACTUAL","INTERVENTIONAL",[55],"NA","This study aims to assess the performances of optical blood pressure monitoring device, Aktiia.product in the context of cardiac rehabilitation program.",[58,59],"Blood Pressure","Hypertension","COMPLETED","2023-01-23",{"date":63,"type":52},"2023-01-25",{"date":65,"type":52},"2020-08-06",{"date":67,"type":52},"2022-12-23",{"name":35,"class":6},1]