[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100623542":3},{"organization":4,"armGroups":7,"interventions":13,"overallOfficials":19,"centralContacts":24,"locations":29,"responsibleParty":45,"collaborators":10,"id":47,"slug":48,"hasResults":49,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":10,"eligibilityCriteria":53,"healthyVolunteers":49,"sex":54,"minAge":55,"maxAge":10,"enrollmentInfo":56,"targetDuration":10,"studyType":59,"phases":10,"briefSummary":60,"conditions":61,"keywords":63,"overallStatus":68,"whyStopped":10,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":78},{"fullName":5,"class":6},"University Hospital, Basel, Switzerland","OTHER",[8],{"label":9,"type":10,"description":10,"interventionNames":11},"Ingestible temperature capsule",null,[12],"Device: Continuous Temperature Monitoring",[14],{"type":15,"name":16,"description":17,"armGroupLabels":18,"otherNames":10},"DEVICE","Continuous Temperature Monitoring","Participants wear investigational temperature sensors and ingest a core temperature capsule continuous data collection",[9],[20],{"name":21,"affiliation":22,"role":23},"Jens Eckstein, Prof. MD","University Hospital of Basel","STUDY_CHAIR",[25],{"name":21,"role":26,"phone":27,"phoneExt":10,"email":28},"CONTACT","0041-61-3287689","jens.eckstein@usb.ch",[30],{"facility":31,"status":10,"city":32,"state":10,"zip":33,"country":34,"countryCode":35,"cosmosGeoPoint":36,"geoPoint":41,"contacts":42},"University Hospital Basel","Basel","4031","Switzerland","CH",{"type":37,"coordinates":38},"Point",[39,40],7.57327,47.55839,{"lat":40,"lon":39},[43],{"name":44,"role":26,"phone":27,"phoneExt":10,"email":28},"Jens Eckstein, Prof. MD.",{"type":46,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100623542","feasibility-of-wearable-based-continuous-temperature-monitoring-100623542",false,"NCT07397988","Feasibility of Wearable-Based Continuous Temperature Monitoring","Feasibility Study for Logistics and Data Stability of Continuous Temperature Monitoring Using a Wearable Device With a Continuous Core Temperature Reference Method","Inclusion Criteria:\n\n* Written informed consent obtained prior to any project-specific procedures.\n* Age 18 years or older at enrolment.\n* Able and willing to comply with project procedures, including capsule ingestion, continuous wearable use for around 48 hours, and adherence to study instructions.\n* Able to swallow the ingestible temperature capsule without difficulty.\n* No contraindication to ingestible thermometry as assessed by the investigator.\n\nExclusion Criteria:\n\nGeneral:\n\n* Body weight \\\u003C 36 kg.\n* Women who are pregnant.\n* Participation in another clinical investigation involving an investigational medicinal product or medical device within the 30 days preceding enrolment or previous enrolment in the current project.\n* Enrolment of the Principal Investigator, project staff, their family members, employees, or other dependent persons.\n* Inability to provide valid informed consent or significant language barrier preventing adequate understanding of procedures.\n\nImplants \\& MRI:\n\n* Presence of any active Implantable Medical Device (AIMD), including Pacemakers, Implantable Cardioverter Defibrillators (ICDs), Deep Brain Stimulation (DBS) devices, or Left Ventricular Assist Devices (LVADs).\n* Requirement for MRI scanning during the seven days following the capsule intake.\n\nCognitive\u002FPhysical Status:\n\n* Unconscious patients (prior to ingestion).\n* Patients with special needs or disabilities preventing safe autonomous swallowing.\n\nGastrointestinal:\n\n* Known history of dysphagia or gag reflex troubles.\n* Previous gastrointestinal surgery resulting in bowel stenosis.\n* Current or planned surgical procedures on the GI tract (esophagus, stomach, intestines).\n* Zenker's diverticulum or felinization of the esophagus.\n* Risk or history of intestinal obstruction, strictures, or diverticula.\n* Hypomotility disorders (e.g., ileus).\n* Inflammatory Bowel Diseases including Crohn's disease or Ulcerative Colitis.\n\nDermatological Exclusions (Rheo Vital+ Performance)\n\n* Dermatological conditions, wounds, tattoos, oedema, inflammation, active venous access, or other impairments at the medial upper arm or axillary region that could interfere with correct placement or functioning of the wearable device.\n* Excessive hair or concurrent devices that hinder correct sensor placement.\n* Known allergy to plastics or latex.\n\nTemperature Management:\n\n* Active external heating or cooling (e.g., cooling blankets).\n* Note: Use of pharmacological antipyretics (oral\u002FIV) is permitted.\n\nFurther Medical Conditions:\n\n* Currently existing acute back pain.\n* Symptomatic herniated disc.","ALL","18 Years",{"count":57,"type":58},12,"ESTIMATED","OBSERVATIONAL","The aim of this study is to evaluate the feasibility of collecting synchronised continuous temperature data using wearable devices and a continuous core temperature reference under real-world conditions. The study focuses on workflow execution, data continuity, secure retrieval, and time-alignment without diagnostic or therapeutic intent.",[62],"Temperature Change, Body",[64,65,66,9,67],"Continuous temperature monitoring","Wearable devices","Feasibility study","Real-world monitoring","NOT_YET_RECRUITING","2026-02-02",{"date":71,"type":72},"2026-02-09","ACTUAL",{"date":74,"type":58},"2026-03",{"date":76,"type":58},"2027-03",{"name":5,"class":6},1]