[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100579812":3},{"organization":4,"armGroups":7,"interventions":21,"overallOfficials":36,"centralContacts":40,"locations":47,"responsibleParty":60,"collaborators":62,"id":66,"slug":67,"hasResults":68,"nctId":69,"briefTitle":70,"officialTitle":71,"acronym":27,"eligibilityCriteria":72,"healthyVolunteers":68,"sex":73,"minAge":74,"maxAge":27,"enrollmentInfo":75,"targetDuration":27,"studyType":78,"phases":79,"briefSummary":81,"conditions":82,"keywords":84,"overallStatus":49,"whyStopped":27,"lastUpdateSubmitDate":88,"lastUpdatePostDateStruct":89,"startDateStruct":92,"completionDateStruct":94,"leadSponsor":96,"locationsCount":97},{"fullName":5,"class":6},"NYU Langone Health","OTHER",[8,16],{"label":9,"type":10,"description":11,"interventionNames":12},"mHealth-Cardiac Rehabilitation (CR)","EXPERIMENTAL","Participants in the mHealth-CR arm will receive daily therapist-directed activity and weekly phone calls, use a mHealth-CR app to track activity, heart rate and access educational materials, and use a wearable wrist activity monitoring device (such as Fitbit or Apple Watch).",[13,14,15],"Behavioral: Communication with exercise therapist","Behavioral: mHealth-CR","Behavioral: Wearable activity monitoring device",{"label":17,"type":18,"description":19,"interventionNames":20},"Usual Care","ACTIVE_COMPARATOR","Participants in usual care arm will receive standard medical care as determined by their physician. They will also use a wearable wrist activity monitoring device.",[15],[22,28,32],{"type":23,"name":24,"description":25,"armGroupLabels":26,"otherNames":27},"BEHAVIORAL","Communication with exercise therapist","A personalized exercise program will be designed. The assigned therapist will identify potential barriers to this plan and develop mitigation strategies. The assigned therapist will then make phone contact with participants weekly for the duration of the study. Exercise recommendations will be titrated during calls based on review of activity data.",[9],null,{"type":23,"name":29,"description":30,"armGroupLabels":31,"otherNames":27},"mHealth-CR","mHealth-CR software (currently, from Corrie Health) will permit 1) participant data entry about exercise; 2) viewing of educational material pertinent to the condition.",[9],{"type":23,"name":33,"description":34,"armGroupLabels":35,"otherNames":27},"Wearable activity monitoring device","Participants will be offered the Fitbit Charge 5. This commercially available product measures physical activity.",[17,9],[37],{"name":38,"affiliation":5,"role":39},"Harmony Reynolds, MD","PRINCIPAL_INVESTIGATOR",[41,45],{"name":38,"role":42,"phone":43,"phoneExt":27,"email":44},"CONTACT","212-263-7751","INOCA@nyulangone.org",{"name":46,"role":42,"phone":43,"phoneExt":27,"email":44},"John Dodson, MD",[48],{"facility":5,"status":49,"city":50,"state":50,"zip":51,"country":52,"countryCode":53,"cosmosGeoPoint":54,"geoPoint":59,"contacts":27},"RECRUITING","New York","10016","United States","US",{"type":55,"coordinates":56},"Point",[57,58],-74.00597,40.71427,{"lat":58,"lon":57},{"type":61,"investigatorFullName":27,"investigatorTitle":27,"investigatorAffiliation":27,"oldNameTitle":27,"oldOrganization":27},"SPONSOR",[63],{"name":64,"class":65},"National Heart, Lung, and Blood Institute (NHLBI)","NIH","100579812","mhealth-cardiac-rehabilitation-for-inoca-100579812",false,"NCT06829160","mHealth-CArdiac REhabilitation for INOCA","mHealth-CArdiac REhabilitation for INOCA (INOCA-CARE)","Inclusion Criteria:\n\n* Age 18 and over\n* Diagnosis of Ischemia with Non-Obstructive Coronary Arteries (INOCA) based on evidence of ischemia and\u002For ischemic symptoms, plus non-obstructive Coronary artery disease (CAD) on computed tomography (CT) or invasive angiography\n\nExclusion Criteria:\n\n* Seattle Angina Questionnaire (SAQ) = 100\n* Non-ambulatory\n* Pregnant\n* Moderate or severe cognitive impairment\n* Unable\u002Fwilling to provide consent\n* Incarcerated\n* Unable to use mHealth\n* Severe osteoarthritis or joint replacement within 3 months\n* Parkinsons disease or other movement disorders\n* Regular use of walker\n* Life expectancy \\\u003C 12 months\n* Clinical judgement concerning other safety or non-adherence issues\n* Unable to read and communicate in English since the app content is currently only available in English.","ALL","18 Years",{"count":76,"type":77},250,"ESTIMATED","INTERVENTIONAL",[80],"NA","This is a multi-site phase II, 2:1 pragmatic randomized trial of 250 participants within the NYU Langone Health (NYULH) and Emory University Medical Center system to evaluate mobile health cardiac rehabilitation (mHealth-CR) in patients who meet clinical criteria for INOCA (ischemia and no obstructive coronary disease on imaging). Participants will be randomized to mHealth-CR or usual care. The study intervention takes place for 3 months which is the time period for most traditional CR programs.\n\nThe overall study goals are threefold: 1) to evaluate whether an mHealth-CR intervention that includes activity tracking, weekly counseling, and exercise documentation, improves health status (i.e., symptoms, function, and quality of life) in patients with INOCA at 3 months; 2) to evaluate effects of the mHealth-CR intervention vs. usual care on physical activity and exercise capacity, general health status, and depressive symptoms (secondary endpoints). We will also evaluate effects on primary and secondary outcomes at 6 months and 1 year; and 3) to characterize engagement and elucidate any factors that limit engagement.",[83],"Ischemia",[85,86,83,87],"INOCA","ANOCA","no obstructive coronary artery disease","2026-04-21",{"date":90,"type":91},"2026-04-23","ACTUAL",{"date":93,"type":91},"2025-03-21",{"date":95,"type":77},"2029-05",{"name":5,"class":6},1]