[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"diagnosis-of-cancer\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:diagnosis-of-cancer":25},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":26,"whyStopped":4,"lastUpdateSubmitDate":27,"lastUpdatePostDateStruct":28,"startDateStruct":31,"completionDateStruct":33,"leadSponsor":35,"locationsCount":4},"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":20,"type":21},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.",[25],"Diagnosis of Cancer","NOT_YET_RECRUITING","2026-07-14",{"date":29,"type":30},"2026-07-17","ACTUAL",{"date":32,"type":21},"2026-09-01",{"date":34,"type":21},"2028-09-01",{"name":36,"class":37},"European Organisation for Research and Treatment of Cancer - EORTC","NETWORK"]