About this trial
This study aims to evaluate how walking stability and the ability to perform daily activities change during cancer treatment, and whether a smartwatch can detect these changes. The goal is to develop proactive, personalized tools that automatically monitor treatment response and predict potential complications. To support future implementation, the study will assess the feasibility of wearing a smartwatch for at least 12 hours per day, using a mobile application, and completing weekly questionnaires among patients with primary osteosarcoma or metastatic bone disease.
Eligibility criteria
Qualifiers
primary sarcoma or metastatic bone disease of the lower extremities or pelvis.
undergoing evaluation for (or have recently undergone) non-surgical or surgical intervention.
recent history of home ambulation.
Disqualifiers
under 18 years of age at the time of study enrolment
inability to comprehend consent form and give informed consent
no access to a smartphone (iOS or Android) to interface with watch application
tattoos located on the skin of the wrist or forearm where the watch will be placed or other skin conditions preventing adequate sensor function
Trial design
Treatments tested in this trial
- Smart Watch