[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"pharmacies\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:pharmacies":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":40,"whyStopped":4,"lastUpdateSubmitDate":41,"lastUpdatePostDateStruct":42,"startDateStruct":45,"completionDateStruct":47,"leadSponsor":49,"locationsCount":5},"100637216","pharmacy-based-opportunistic-atrial-fibrillation-screening-integrated-with-emergency-services-numaplus-fa-100637216",false,"NCT07598903","Pharmacy-based Opportunistic Atrial Fibrillation Screening Integrated With Emergency Services (NUMAPLUS-FA)","Pharmacy-based Opportunistic Screening for Atrial Fibrillation Using a Portable ECG Device Integrated With Emergency Medical Services: a Prospective Type-1 Hybrid Implementation Study (NUMAPLUS Project)","Numaplus_FA","Inclusion Criteria:\n\n1. Age 65 years or older\n2. Attending a participating community pharmacy for any routine healthcare purpose\n3. No prior documented or patient-reported diagnosis of atrial fibrillation\n4. Capacity to provide written informed consent\n\nExclusion Criteria:\n\n1. Confirmed prior diagnosis of atrial fibrillation\n2. Implanted pacemaker, implantable cardioverter-defibrillator (ICD) or other intracardiac device\n3. Clinically evident haemodynamic instability requiring direct emergency 061 activation (active chest pain, severe dyspnoea, syncope)\n4. Concurrent participation in another cardiac rhythm monitoring study\n5. Inability to maintain the required position for a 30-second ECG recording","ALL","65 Years",{"count":20,"type":21},380,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study evaluates the feasibility and fidelity of an opportunistic atrial fibrillation (AF) screening programme conducted in 38 community pharmacies in Seville (Spain), using the Kardias® 6-lead portable ECG device, coordinated with the emergency medical services centre Salud Responde (CES 061) and primary care physicians. Eligible participants are individuals aged 65 years or older without a prior AF diagnosis who attend a participating pharmacy for any routine purpose. The screening consists of a 30-second ECG recording performed by a trained community pharmacist. Positive or indeterminate results are transmitted in real time to Salud Responde for clinical validation and referral to primary care. The study is evaluated using the RE-AIM framework (Reach, Effectiveness, Adoption, Implementation, Maintenance). The primary outcome is protocol fidelity, measured by the Implementation Adherence Grade (IAG). The study is part of the NUMAPLUS project, funded by INTERREG VI-A España-Portugal (POCTEP 2021-2027), co-financed by the European Regional Development Fund (ERDF).",[27,28,29,30],"Atrial Fibrillation (Prevention of Stroke)","Arrythmia, Cardiac","Mass Screening","Pharmacies",[32,33,34,35,36,37,38,39],"atrial fibrillation","opportunistic screening","community pharmacy","RE-AIM","implementation science","emergency medical services","portable ECG","hybrid implementation study","NOT_YET_RECRUITING","2026-05-20",{"date":43,"type":44},"2026-05-22","ACTUAL",{"date":46,"type":21},"2026-06-01",{"date":48,"type":21},"2026-12-31",{"name":50,"class":51},"Centro de Emergencias Sanitarias 061 Andalucía","OTHER"]