[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100595642":3},{"organization":4,"armGroups":7,"interventions":24,"overallOfficials":35,"centralContacts":40,"locations":49,"responsibleParty":63,"collaborators":12,"id":67,"slug":68,"hasResults":69,"nctId":70,"briefTitle":71,"officialTitle":72,"acronym":73,"eligibilityCriteria":74,"healthyVolunteers":69,"sex":75,"minAge":76,"maxAge":77,"enrollmentInfo":78,"targetDuration":12,"studyType":81,"phases":82,"briefSummary":84,"conditions":85,"keywords":89,"overallStatus":52,"whyStopped":12,"lastUpdateSubmitDate":102,"lastUpdatePostDateStruct":103,"startDateStruct":106,"completionDateStruct":108,"leadSponsor":110,"locationsCount":111},{"fullName":5,"class":6},"Ludwig Boltzmann Gesellschaft","OTHER",[8,13,19],{"label":9,"type":10,"description":11,"interventionNames":12},"Standard care","NO_INTERVENTION","Participants receive standard ICU follow-up care at the Medical University of Vienna without wearable devices or digital health tools.",null,{"label":14,"type":15,"description":16,"interventionNames":17},"Wearables Only","EXPERIMENTAL","Participants receive wearable health monitoring devices (Garmin Vivosmart 5, Garmin Index S2 Smart Scale, Garmin Index BPM blood pressure monitor) and use the Fitrockr application to visualize and track their data. No counseling or bi-weekly summaries are provided.",[18],"Device: Wearable Health Monitoring",{"label":20,"type":15,"description":21,"interventionNames":22},"Wearables + Summary + Counseling","Participants receive the same wearable devices and Fitrockr app as the Wearables Only group. In addition, they receive bi-weekly automatically generated health summaries via email and have the option to book lifestyle consultations with a member of the study team via Webex.",[18,23],"Behavioral: Digital Health Summary and Lifestyle Counseling",[25,30],{"type":26,"name":27,"description":28,"armGroupLabels":29,"otherNames":12},"DEVICE","Wearable Health Monitoring","Participants receive a Garmin Vivosmart 5, Garmin Index S2 Smart Scale, and Garmin Index BPM blood pressure monitor for daily health tracking. Devices sync to the Fitrockr mobile application.",[20,14],{"type":31,"name":32,"description":33,"armGroupLabels":34,"otherNames":12},"BEHAVIORAL","Digital Health Summary and Lifestyle Counseling","Participants receive bi-weekly health summaries via email generated from wearable data and may opt in to monthly video-based lifestyle consultations with trained study staff.",[20],[36],{"name":37,"affiliation":38,"role":39},"Harald Willschke, Ao. Univ. Prof. Dr.","Medical University of Vienna \u002F Ludwig Boltzmann Institute for Digital Health and Patient Safety","STUDY_DIRECTOR",[41,46],{"name":42,"role":43,"phone":44,"phoneExt":12,"email":45},"Akos Tiboldi, Dr.med.univ.","CONTACT","+43 660 7432550","akos.tiboldi@lbg.ac.at",{"name":47,"role":43,"phone":12,"phoneExt":12,"email":48},"Lisa Lichtenegger, BSc MSc","lisa.lichtenegger@lbg.ac.at",[50],{"facility":51,"status":52,"city":53,"state":12,"zip":54,"country":55,"countryCode":56,"cosmosGeoPoint":57,"geoPoint":62,"contacts":12},"Ludwig Boltzmann Institute Digital Health and Patient Safety","RECRUITING","Vienna","1090","Austria","AT",{"type":58,"coordinates":59},"Point",[60,61],16.37208,48.20849,{"lat":61,"lon":60},{"type":64,"investigatorFullName":65,"investigatorTitle":66,"investigatorAffiliation":5,"oldNameTitle":12,"oldOrganization":12},"PRINCIPAL_INVESTIGATOR","Akos Tiboldi","Principal Investigator","100595642","i-wear-evaluating-wearables-and-health-summaries-in-icu-survivors-100595642",false,"NCT07035106","I-WEAR: Evaluating Wearables and Health Summaries in ICU Survivors","I-WEAR: From ICU to Recovery - Evaluating the Feasibility and Usability of Bi-Weekly Health Summaries Using Wearables in Patients After Intensive Care Unit Treatment - A Pilot Study","I-WEAR","Inclusion Criteria:\n\n* Age 18-65 years at the time of ICU admission\n* ICU stay of at least 48 hours\n* ICU discharge within the last 2 years\n* Comorbidity of diabetes mellitus and\u002For chronic heart failure\u002Fcoronary artery disease\n* Written informed consent\n* Access to a home internet connection and smartphone with internet and Bluetooth\n\nExclusion Criteria:\n\n* Presence of a legal guardian\n* No smartphone or internet access\n* No cardiovascular disease\u002Fevent and\u002For diabetes\n* Implanted pacemaker or defibrillator\n* Allergies to materials in the wearable devices\n* Transfer from an ICU outside the Medical University of Vienna\n* Homelessness\n* Residence outside of Austria","ALL","18 Years","65 Years",{"count":79,"type":80},60,"ESTIMATED","INTERVENTIONAL",[83],"NA","This pilot study investigates the use of wearable health technology and bi-weekly digital health summaries in patients recovering from intensive care. Many patients experience physical, psychological, and cognitive challenges after an ICU stay, a condition known as Post-Intensive Care Syndrome (PICS). The study aims to evaluate the feasibility and usability of wearable devices-such as smartwatches, blood pressure monitors, and smart scales-for tracking recovery in real-world settings.\n\nParticipants will be randomly assigned to one of three groups: standard ICU follow-up care, wearable use only, or wearable use combined with bi-weekly health reports and optional lifestyle consultations. The study will assess participants' quality of life, experience using the technology, and adherence over a 6-month period. Results will inform the future use of digital tools in post-ICU care.",[86,87,88],"Post-Intensive Care Syndrome (PICS)","Critical Illness Recovery","Coronary Artery Disease",[90,91,92,93,94,95,96,97,98,99,100,101],"Wearables","Health-related quality of life","ICU survivors","Digital health","Remote patient monitoring","System Usability Scale","SF-36","Bi-weekly health summary","Pilot study","PICS","Cardiovascular disease","Diabetes","2025-09-02",{"date":104,"type":105},"2025-09-09","ACTUAL",{"date":107,"type":105},"2025-07-01",{"date":109,"type":80},"2026-05-30",{"name":5,"class":6},1]