[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100595885":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":30,"centralContacts":34,"locations":43,"responsibleParty":62,"collaborators":65,"id":69,"slug":70,"hasResults":71,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":75,"eligibilityCriteria":76,"healthyVolunteers":71,"sex":77,"minAge":78,"maxAge":26,"enrollmentInfo":79,"targetDuration":26,"studyType":82,"phases":83,"briefSummary":85,"conditions":86,"keywords":92,"overallStatus":46,"whyStopped":26,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":109},{"fullName":5,"class":6},"Institut d'Investigació Biomèdica de Bellvitge","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Standard of care","ACTIVE_COMPARATOR","Usual cardiac rehabilitation program",[13],"Other: Usual Care",{"label":15,"type":16,"description":17,"interventionNames":18},"Personalized intervention program","EXPERIMENTAL","BREAK intervention group with more alternatives of aerobic and strength exercises and also offering remote options for fragile patients",[19],"Behavioral: Personalised treatment",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"BEHAVIORAL","Personalised treatment","Patients going through a personalized intervention program",[15],null,{"type":6,"name":28,"description":11,"armGroupLabels":29,"otherNames":26},"Usual Care",[9],[31],{"name":32,"affiliation":5,"role":33},"Cristina Enjuanes, MD, PhD","PRINCIPAL_INVESTIGATOR",[35,40],{"name":36,"role":37,"phone":38,"phoneExt":26,"email":39},"Cristina Enjuanes Grau, MD, PhD","CONTACT","+34 93 260 7078","cenjuanes@bellvitgehospital.cat",{"name":41,"role":37,"phone":38,"phoneExt":26,"email":42},"Pablo Morales, MD","pmorales@idibell.cat",[44],{"facility":45,"status":46,"city":47,"state":48,"zip":49,"country":50,"countryCode":51,"cosmosGeoPoint":52,"geoPoint":57,"contacts":58},"Hospital Universitari de Bellvitge","RECRUITING","L'Hospitalet de Llobregat","Barcelona","08907","Spain","ES",{"type":53,"coordinates":54},"Point",[55,56],2.10028,41.35967,{"lat":56,"lon":55},[59],{"name":41,"role":37,"phone":60,"phoneExt":26,"email":61},"686385245","cristinaenjuanes@gmail.com",{"type":33,"investigatorFullName":63,"investigatorTitle":64,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"Cristina Enjuanes Grau","Coordinator of Community Heart Failure Unit, Cardiology Department. MD, PhD",[66,67],{"name":45,"class":6},{"name":68,"class":6},"Fundació La Marató de TV3","100595885","patient-centered-personalized-cardiac-rehabilitation-in-post-acute-coronary-syndrome-break-trial-100595885",false,"NCT07038265","Patient-centered Personalized Cardiac Rehabilitation in Post Acute Coronary Syndrome (BREAK-trial)","Patient-centered Cardiac rehaBilitation pRogramE in Post Acute Coronary Syndrome:Identification of Key Barriers and Evaluation of Personalized Intervention (BREAK-trial)","BREAK","Inclusion Criteria:\n\n1. Patient aged ≥ 18 years\n2. Patients discharged within the last 30 days after an admission for ACS or in the discharge planning process for an admission for ACS.\n3. The patient is able to fully communicate with the research team and comply with all study procedures.\n4. The patient voluntarily signs and dates the informed consent form approved by the ethics committee\n\nExclusion Criteria:\n\n1. Age \\\u003C18 years\n2. Participation in another clinical trial\n3. Moderate or severe cognitive impairment in the absence of a competent caregiver\n4. Absence of social support\n5. Institutionalized patient\n6. Life expectancy \\\u003C1 year\n7. Candidates for end-of-life care\n8. Severe psychiatric illness\n9. Planned cardiac surgery including transplant or circulatory support implant\n10. Death before hospital discharge in patients included in the hospital discharge planning phase\n11. Carrier of heart transplant.\n12. Patient unable or refusing to give written informed consent to participate\n13. Patients who, in the opinion of the investigator, are unsuitable candidates for the study","ALL","18 Years",{"count":80,"type":81},202,"ESTIMATED","INTERVENTIONAL",[84],"NA","The primary objective of this study is to compare an integrated, multidisciplinar patient-centered CRP (Cardiac Rehabilitation Program) (intervention group) especially focused on covering the needs for the female and fragile population to the usual care conventional CRP (control group)",[87,88,89,90,91],"Acute Coronary Syndromes (ACS)","Cardiac Rehabilitation","Frailty","Women","Women's Health",[93,94,95,96,97,98,99],"frailty","sarcopenia","cardiac rehabilitation","gender perspective","acute coronary syndrome","coronary artery disease","patient-centered care","2025-06-17",{"date":102,"type":103},"2025-06-26","ACTUAL",{"date":105,"type":103},"2025-05-26",{"date":107,"type":81},"2027-11",{"name":5,"class":6},1]