[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100647572":3},{"organization":4,"armGroups":7,"interventions":7,"overallOfficials":7,"centralContacts":8,"locations":7,"responsibleParty":14,"collaborators":7,"id":16,"slug":17,"hasResults":18,"nctId":19,"briefTitle":20,"officialTitle":21,"acronym":22,"eligibilityCriteria":23,"healthyVolunteers":18,"sex":24,"minAge":25,"maxAge":7,"enrollmentInfo":26,"targetDuration":7,"studyType":29,"phases":7,"briefSummary":30,"conditions":31,"keywords":7,"overallStatus":33,"whyStopped":7,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":7},{"fullName":5,"class":6},"European Organisation for Research and Treatment of Cancer - EORTC","NETWORK",null,[9],{"name":10,"role":11,"phone":12,"phoneExt":7,"email":13},"EORTC HQ","CONTACT","+32 2 774 1611","2124@eortc.org",{"type":15,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR","100647572","eortc-mobile-device-embed-100647572",false,"NCT07711080","Eortc MoBilE Device (EMBED)","Eortc MoBilE Device (EMBED) - Implementation of Smart Devices for the Assessment of Quality of Life, Patient Reported Outcomes (PROs) and Physical Functioning and Activity in EORTC Clinical Trials: A Feasibility Study.","EMBED","Inclusion Criteria:\n\n* Diagnosis of cancer\n* Age≥18\n* Starting a first or new anticancer treatment within one month following enrolment\n* Literacy in the target language\n* Ability to understand and fill out questionnaires\n* Ability to operate a smartphone\n* In possession of a smartphone allowing for an internet connection and willing to use this device to submit data\n* Written informed consent\n* Life expectancy\\>3 months\n\nExclusion Criteria:\n\n* Exclusively receiving palliative care\n* Start of cancer-related treatment \\\u003C 1 week from time of screening\n* Any psychological, familial, sociological or geographical condition potentially hampering compliance with the study protocol and follow-up schedule; those conditions should be assessed and discussed with the patient before enrolment in this study.","ALL","18 Years",{"count":27,"type":28},137,"ESTIMATED","OBSERVATIONAL","This study is a longitudinal observational study that will investigate the feasibility of using mobile devices for the assessment of HRQoL and physical activity in adult cancer patients undergoing treatment. Patients will complete a set of patient reported outcome measures (PROMs), and wear a smartwatch (min. 10 hours per day for one week), at baseline, and at weeks 4, 8 and 12 after treatment start.",[32],"Diagnosis of Cancer","NOT_YET_RECRUITING","2026-07-14",{"date":36,"type":37},"2026-07-17","ACTUAL",{"date":39,"type":28},"2026-09-01",{"date":41,"type":28},"2028-09-01",{"name":5,"class":6}]