[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100614156":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":24,"centralContacts":28,"locations":34,"responsibleParty":52,"collaborators":18,"id":54,"slug":55,"hasResults":56,"nctId":57,"briefTitle":58,"officialTitle":59,"acronym":18,"eligibilityCriteria":60,"healthyVolunteers":56,"sex":61,"minAge":62,"maxAge":18,"enrollmentInfo":63,"targetDuration":18,"studyType":66,"phases":67,"briefSummary":69,"conditions":70,"keywords":72,"overallStatus":37,"whyStopped":18,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":84,"completionDateStruct":86,"leadSponsor":88,"locationsCount":89},{"fullName":5,"class":6},"Linkoeping University","OTHER_GOV",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Tailored implementation","EXPERIMENTAL","This arm will receive tailored implementation support.",[13],"Other: Tailored implementation support",{"label":15,"type":16,"description":17,"interventionNames":18},"Control","NO_INTERVENTION","This group will receive standard implementation of the support program.",null,[20],{"type":21,"name":22,"description":22,"armGroupLabels":23,"otherNames":18},"OTHER","Tailored implementation support",[9],[25],{"name":26,"affiliation":5,"role":27},"Anna Stroemberg","PRINCIPAL_INVESTIGATOR",[29],{"name":30,"role":31,"phone":32,"phoneExt":18,"email":33},"Anna Stroemberg, Professor","CONTACT","+46736569265","anna.stromberg@liu.se",[35],{"facility":36,"status":37,"city":38,"state":39,"zip":40,"country":41,"countryCode":42,"cosmosGeoPoint":43,"geoPoint":48,"contacts":49},"Linköping University Hospital","RECRUITING","Linköping","Östergötland County","581 85","Sweden","SE",{"type":44,"coordinates":45},"Point",[46,47],15.62157,58.41086,{"lat":47,"lon":46},[50],{"name":51,"role":31,"phone":32,"phoneExt":18,"email":33},"Anna Strömberg, PhD",{"type":27,"investigatorFullName":26,"investigatorTitle":53,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"Professor","100614156","digital-support-program-for-patients-with-heart-failure---a-cluster-randomized-hybrid-type-2-study-100614156",false,"NCT07275931","Digital Support Program for Patients With Heart Failure - a Cluster-Randomized Hybrid Type 2 Study","Digital Support Program Via 1177 for Patients With Heart Failure - a Cluster-Randomized Hybrid Type 2 Study for Evaluation of Effects and Implementation","Inclusion criteria:\n\n* Diagnosed with heart failure with reduced ejection fraction (HFrEF) or heart failure with midrange reduced ejection fraction (HFmrEF) (ejection fraction ≤50%) verified by echocardiography or Magnetic Resonance Imaging\n* Access to BankID, a computer, tablet, or smartphone\n* Aged ≥18 years\n* Able to understand and communicate in Swedish\n* Provided informed consent\n\nExclusion criteria:\n\n* Barriers to participation (e.g., not Swedish-speaking, cognitive impairment, severe mental illness, substance abuse)\n* Life expectancy of less than six months","ALL","18 Years",{"count":64,"type":65},240,"ESTIMATED","INTERVENTIONAL",[68],"NA","The overall aim of this project is to evaluate the effects of a digital support program for patients with heart failure through a cluster-randomized controlled trial, and to investigate the outcomes of different implementation strategies using the RE-AIM (Reach, Effectiveness, Adoption, Implementation, Maintenance), PRISM (Practical, Robust Implementation and Sustainability Model) and ERIC (Expert Recommendations for Implementing Change) framework.\n\nOur primary hypothesis is that the digital support program will improve patients' perceived control over their heart failure, measured with the validated Control Attitude Scale.\n\nSecondary hypotheses are that the program will increase patients' health-related quality of life, self-care behaviors, heart failure knowledge, perceived continuity of care, and participation in care, and reduce symptoms of depression.\n\nImplementation aim (based on the RE-AIM, PRISM and ERIC frameworks) The implementation component of the study aims to compare two different implementation strategies: a standard (basic) support package versus a tailored, context-specific support strategy.\n\nHeart failure clinics at hospitals an within primary care will be matched and randomized into two arms. The intervention arm will receive tailored implementation support to implement the support program. The control arm will recive implementation support according to a predefined standard procedure.\n\nResearchers will compare the intervention arm with control arm to see if there are any differences regarding the implementationsuccess between the arms.\n\nThe patients in both arms will have access to the support program during six months.",[71],"Heart Failure With Reduced Ejection Fraction",[73,74,75,76,77,78,79],"Co-design","E-health","support","implementation","RE-AIM","PRISM","ERIC","2026-02-24",{"date":82,"type":83},"2026-02-27","ACTUAL",{"date":85,"type":83},"2025-12-15",{"date":87,"type":65},"2029-06-30",{"name":5,"class":6},1]