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NCT07711080
Eortc MoBilE Device (EMBED)
Conditions: Diagnosis of Cancer
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 137
Sponsor: European Organisation for Research and Treatment of Cancer - EORTC
Summary
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.
Eligibility Criteria
Inclusion Criteria:
* Diagnosis of cancer
* Age≥18
* Starting a first or new anticancer treatment within one month following enrolment
* Literacy in the target language
* Ability to understand and fill out questionnaires
* Ability to operate a smartphone
* In possession of a smartphone allowing for an internet connection and willing to use this device to submit data
* Written informed consent
* Life expectancy\>3 months
Exclusion Criteria:
* Exclusively receiving palliative care
* Start of cancer-related treatment \< 1 week from time of screening
* 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.
Source: ClinicalTrials.gov (NCT07711080). StuddyBuddy aggregates publicly available trial information.