[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100650043":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":33,"centralContacts":37,"locations":32,"responsibleParty":43,"collaborators":45,"id":49,"slug":50,"hasResults":51,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":51,"sex":57,"minAge":58,"maxAge":32,"enrollmentInfo":59,"targetDuration":32,"studyType":62,"phases":63,"briefSummary":65,"conditions":66,"keywords":73,"overallStatus":78,"whyStopped":32,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":32},{"fullName":5,"class":6},"University of Illinois at Chicago","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"CBCR only","ACTIVE_COMPARATOR","Participants randomized to the control group will receive standard outpatient CBCR at UI Health with no additional study-delivered mHealth intervention. The CBCR program at UI Health is a structured, medically supervised secondary prevention program for patients with qualifying cardiovascular conditions. It includes individualized aerobic and resistance exercise training, clinical monitoring during exercise sessions, education on heart disease and risk factor management, counseling to promote healthy lifestyle behaviors, and support for long-term adherence to prescribed treatment and self-care recommendations.\n\nParticipants are encouraged to attend up to 36 supervised sessions over \\~12 weeks. In addition to supervised exercise, CBCR includes education related to cardiovascular disease self-management, physical activity, healthy eating, weight management, lipid control, blood pressure management, smoking cessation, stress reduction, and other risk factor modification strtegies.",[13],"Other: CBCR",{"label":15,"type":16,"description":17,"interventionNames":18},"CBCR + BRIDGE","EXPERIMENTAL","Participants randomized to the intervention group will receive BRIDGE in addition to the standard CBCR program at UI Health. BRIDGE is a multimodal mHealth intervention designed to extend behavioral support beyond clinic visits through mobile app- and device-based self-monitoring, feedback, and individually tailored text messages promoting healthy lifestyle behaviors (e.g. physical activity, heart healthy diet, and medication adherence).",[13,19],"Behavioral: BRIDGE mHealth intervention",[21,27],{"type":6,"name":22,"description":23,"armGroupLabels":24,"otherNames":25},"CBCR","The CBCR program at UI Health is a structured, medically supervised secondary prevention program for patients with qualifying cardiovascular conditions. It includes individualized aerobic and resistance exercise training, clinical monitoring during exercise sessions, education on heart disease and risk factor management, counseling to promote healthy lifestyle behaviors, and support for long-term adherence to prescribed treatment and self-care recommendations. Participants are encouraged to attend up to 36 supervised sessions over \\~12 weeks.",[15,9],[26],"Comprehensive CBCR",{"type":28,"name":29,"description":30,"armGroupLabels":31,"otherNames":32},"BEHAVIORAL","BRIDGE mHealth intervention","Description: The intervention includes three commercially available mHealth apps and devices: Withings Body Composition weight scale, Withings BP monitor, and Fitbit Charge 6 activity tracker along with their companion mobile apps. Each app incorporates behavior change tools that support daily self-monitoring, feedback, and reminders across key cardiac rehabilitation domains, including physical activity, weight and blood pressure management, and cardiovascular risk factor reduction. Participants will also receive up to five individually tailored text messages per week throughout the intervention period. Messages will be individualized based on (1) patient responses to validated questionnaires administered at baseline and (2) patient-generated health data from the app\u002Fdevices. Messages will target physical activity, healthy eating, weight management, blood pressure control, and cardiovascular risk reduction.",[15],null,[34],{"name":35,"affiliation":5,"role":36},"Spyros Kitsiou, PhD","PRINCIPAL_INVESTIGATOR",[38],{"name":39,"role":40,"phone":41,"phoneExt":32,"email":42},"Leah Li, MSN, RN","CONTACT","13123553519","yli351@uic.edu",{"type":44,"investigatorFullName":32,"investigatorTitle":32,"investigatorAffiliation":32,"oldNameTitle":32,"oldOrganization":32},"SPONSOR",[46],{"name":47,"class":48},"National Center for Advancing Translational Sciences (NCATS)","NIH","100650043","bridge-trial-embedding-consumer-grade-mhealth-technologies-into-cardiac-rehabilitation-100650043",false,"NCT07741396","BRIDGE Trial: Embedding Consumer-grade mHealth Technologies Into Cardiac Rehabilitation","BRIDGE Trial: Embedding Consumer-grade mHealth Technologies Into Cardiac Rehabilitation as a Model for Chronic Disease Management","BRIDGE","Inclusion Criteria:\n\n1. Adults aged 18 years or older.\n2. Enrolled in or referred to Phase II Center-based Cardiac Rehabilitation Program.\n3. Have a qualifying cardiovascular diagnosis or event that meets standard eligibility for Phase II Center-based Cardiac Rehabilitation, such as:\n\n   * Acute myocardial infarction\n   * Percutaneous coronary intervention\n   * Coronary artery bypass graft surgery\n   * Chronic heart failure with reduced ejection fraction\n   * Heart valve repair or replacement\n   * Stable angina\n4. Able to ambulate and participate in exercise testing and training as required by the CR program\n5. Ability to speak and read in English\n6. Willing and able to provide informed consent.\n7. Willing to use study-related devices\u002Fapps and complete study assessments.\n\nExclusion Criteria:\n\n1. Not enrolled in or not planning to participate in Phase II Center-based Cardiac Rehabilitation Program.\n2. Presence of a medical, cognitive, psychiatric, or physical condition that, in the opinion of the investigators or CR team, would preclude safe participation in the study or adherence to study procedures.\n3. Severe cognitive impairment or active psychiatric illness that would interfere with informed consent or study participation.\n4. Terminal illness or other serious medical condition that in the judgement of the treating clinician or investigator would likely preclude completion of the study follow-up period. .\n5. Current hospice enrollment or residence in a long-term care facility that would preclude participation in the intervention or completion of study follow-up procedures.\n6. Currently participating in another behavioral or digital health intervention trial that could confound study outcomes.\n7. Inability or unwillingness to use the required mobile devices, applications, or monitoring equipment, if applicable.","ALL","18 Years",{"count":60,"type":61},30,"ESTIMATED","INTERVENTIONAL",[64],"NA","The purpose of the BRIDGE study is to learn whether supplementing traditional center-based cardiac rehabilitation (CBCR) with a mobile health technology intervention can help patients monitor their health, stay engaged in healthy lifestyle behaviors, better manage cardiovascular risk factors, and improve overall health outcomes.\n\nCardiac rehabilitation is an evidence-based outpatient program designed to help people recover from heart-related conditions through supervised exercise, education, counseling, and support for healthy lifestyle changes. Although cardiac rehabilitation is highly recommended and beneficial, many patients do not receive the full benefits of the program. Some patients attend fewer sessions than recommended, and many find it difficult to maintain healthy habits outside of the clinic, such as regular physical activity, heart-healthy eating, taking medications as prescribed, monitoring blood pressure, and managing weight.\n\nThis study will test whether combining CBCR with mobile health tools may improve participation and support healthy behaviors at home. Mobile health tools include mobile phone applications, connected devices such as a weight scale, blood pressure monitor, and activity tracker, as well as personalized text messages designed to encourage and support healthy self-care.\n\nThis study will help determine whether these mobile health tools can make cardiac rehabilitation more effective and help patients maintain healthy behaviors beyond the clinic setting.",[67,68,69,70,71,72],"Acute Myocardial Infarction (AMI)","Percutaneous Coronary Intervention (PCI)","Coronary Artery Bypass Graft Surgery (CABG)","Chronic Heart Failure With Reduced Ejection Fraction (HFrEF)","Heart Valve Repair or Replacement","Stable Angina Pectoris",[74,75,76,77],"cardiac rehabilitation","mHealth","digital tool","consumer-grade technology","NOT_YET_RECRUITING","2026-07-29",{"date":81,"type":82},"2026-08-03","ACTUAL",{"date":84,"type":61},"2026-09-01",{"date":86,"type":61},"2027-07-30",{"name":5,"class":6}]