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Not Yet Recruiting 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.

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07711080). StuddyBuddy aggregates publicly available trial information.