[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100542664":3},{"organization":4,"armGroups":7,"interventions":23,"overallOfficials":35,"centralContacts":40,"locations":11,"responsibleParty":48,"collaborators":11,"id":50,"slug":51,"hasResults":52,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":56,"eligibilityCriteria":57,"healthyVolunteers":52,"sex":58,"minAge":59,"maxAge":11,"enrollmentInfo":60,"targetDuration":11,"studyType":63,"phases":64,"briefSummary":66,"conditions":67,"keywords":70,"overallStatus":75,"whyStopped":11,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":80,"completionDateStruct":82,"leadSponsor":84,"locationsCount":11},{"fullName":5,"class":6},"Elsan","OTHER",[8,14,19],{"label":9,"type":10,"description":11,"interventionNames":12},"Individualized physical activity program","EXPERIMENTAL",null,[13],"Other: Individuals activity programs",{"label":15,"type":16,"description":11,"interventionNames":17},"Physical Activity program defined without optimisation","ACTIVE_COMPARATOR",[18],"Other: activity program",{"label":20,"type":6,"description":11,"interventionNames":21},"no Physical Activity program",[22],"Other: no Physical Activity program",[24,28,32],{"type":6,"name":25,"description":26,"armGroupLabels":27,"otherNames":11},"Individuals activity programs","activity program will be adjusted every week by practitioner for each patient following data coming from the wearable device ( connected whatch and bellt for 12 months)",[9],{"type":6,"name":29,"description":30,"armGroupLabels":31,"otherNames":11},"activity program","pre established program without adjustement. The patient has connected whatch and bellt for 12 months",[15],{"type":6,"name":20,"description":33,"armGroupLabels":34,"otherNames":11},"no Physical Activity (PA)program but just PA recommendations.PA is carried out independently (common practice).The patient has connected whatch and bellt for 12 months",[20],[36],{"name":37,"affiliation":38,"role":39},"Deva BAS, MD","Clinique SSR SuperValtech","PRINCIPAL_INVESTIGATOR",[41,46],{"name":42,"role":43,"phone":44,"phoneExt":11,"email":45},"christine Blanc","CONTACT","0468562895","christine.blanc@elsan.care",{"name":37,"role":43,"phone":47,"phoneExt":11,"email":11},"0468874022",{"type":49,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100542664","innovative-care-pathway-in-physical-activity-and-behavior-change-in-coronary-patients-post-cardiac-rehabilitation-100542664",false,"NCT06345807","Innovative Care Pathway in Physical Activity and Behavior Change in Coronary Patients Post-cardiac Rehabilitation","Innovative Care Pathway in Physical Activity and Behavior Change in Coronary Patients Post Cardiac Rehabilitation","APIC","Inclusion Criteria:\n\n* Post-infarction coronary artery patient aged 18 years and older, with no gender difference.\n* Patients engaged in a follow-up care and cardiovascular rehabilitation program at the Supervaltech center.\n* Patient at low to moderate RARE risk of complication (RARE score 2 to 3)\n* Patients equipped with smartphones, laptops or other equipment compatible with downloading an application with their personal ID\n* Patient able to understand French for the purpose of conducting the study.\n* Affiliated member or beneficiary of a social security scheme.\n* Participant who has been informed and has given free, informed and written consent (no later than the day of inclusion and before any examination required by the research).\n\nExclusion Criteria:\n\n* Patients with a formal contraindication to physical activity such as: unstabilized coronary syndrome, decompensated heart failure, severe ventricular arrhythmias, intracardiac thrombus at risk embolic, PAH, moderate pericardial effusion, history of thrombophlebitis with or without pulmonary embolism, severe and\u002For symptomatic left ventricular ejection obstruction.\n* Patients with ongoing infectious disease\n* Participant whose physical and\u002For psychological health is severely impaired, which in the opinion of the investigator may affect the study participant's compliance.\n* Participant included in other research\n* Participant in a period of exclusion from another research still in progress at the time of inclusion.\n* Protected participant: an adult under guardianship, curatorship or other legal protection, deprived of liberty by judicial or administrative decision.\n* Pregnant, breastfeeding or parturient women.\n* Participant hospitalized without consent.","ALL","18 Years",{"count":61,"type":62},192,"ESTIMATED","INTERVENTIONAL",[65],"NA","The objective of this 18-month research is to show the effectiveness of an individualized physical activity( PA) compared to standard PA management and voluntary PA, to achieve a change in the behavior of the coronary patient.",[68,69],"Individualised Physical Activity Program","Coronary Patient",[71,72,73,74],"cardiac rehabilitation","ischemic heart disease","physical activity","wearables","NOT_YET_RECRUITING","2024-08-30",{"date":78,"type":79},"2024-09-03","ACTUAL",{"date":81,"type":62},"2024-10",{"date":83,"type":62},"2026-11",{"name":5,"class":6}]