Feasibility Study of the Advanced Symptom Management System (ASyMS) in Canadian Cancer Patients

NACompletedINTERVENTIONAL
Enrollment

84

Participants

Timeline

Start Date

November 15, 2017

Primary Completion Date

February 28, 2019

Study Completion Date

May 28, 2019

Conditions
Supportive CareCancer
Interventions
DEVICE

ASyMS-Can

Data reported by the participants will be sent to a secure, encrypted clinical central server hosting the risk-alerting algorithms. The web interfaces will provide a clinical portal for the nurses to screen and follow any alerts being triggered, as well as review patient-specific information. Based on these back-end computations, participants will receive automated self-care notifications on their mobile phones. If incoming symptom reports indicate severe adverse effects a designated clinic nurse will receive an 'amber alert', or 'red alert', that will require response within 30 minutes. Nurses will handle alerts during business hours (9 am to 5 pm). After-hour alerts will be sent to the oncologist or nursing supervisor on call as per usual care. Patients will be instructed that clinicians will not receive alerts during the evening hours or night and instructed to follow usual practice of contacting their family physician, or oncologist on call, or call 911, as required.

Trial Locations (1)

Unknown

Princess Margaret Cancer Centre, Toronto

All Listed Sponsors
collaborator

Canadian Institutes of Health Research (CIHR)

OTHER_GOV

lead

University Health Network, Toronto

OTHER

NCT03335189 - Feasibility Study of the Advanced Symptom Management System (ASyMS) in Canadian Cancer Patients | Biotech Hunter | Biotech Hunter