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Study identifier: NCT07024329 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Implementing REmote SymPtom mOnitoring and maNagement (RESPONd)

Condition: Cancer  ·  Sponsor: University of Calgary

PhaseNA
Planned participants1055
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this study is to understand if the implementation of a remote symptom monitoring and management program improves outcomes. The program will provide patients the opportunity to complete electronic Patient Reported Outcomes (PROs) questionnaires from home between appointments and receive tailored advice from a study nurse. A second goal of this study is to examine the impact of electronic symptom monitoring on clinic efficiencies. The main question it aims to answer is: • What impact does implementing digitally enabled remote symptom monitoring and management (RESPONd) between ambulatory oncology visits have on patient outcomes and system efficiencies? Participants will: * Report their symptoms and concerns from home by completing the electronic symptom monitoring questionnaire. * Discuss their symptoms and concerns with a study nurse. * Provide feedback about their experience at important timepoints during the study. * Participate as usual in ambulatory clinic appointments.

This description comes directly from the study's public registry record.

Talk to the study team

Chizoba Anyimukwu, MPH, DrPH  ·  587-943-3556  ·  chizoba.anyimukwu@albertahealthservices.ca

Benedicta Asante, RSW, MSW  ·  587-943-3562  ·  benedicta.asante@albertahealthservices.ca

Always discuss trial participation with your own doctor first.

Locations (4)

Arthur J. E. Child Comprehensive Cancer CentreCalgary, Alberta, CanadaRecruiting
Cross Cancer InstituteEdmonton, Alberta, CanadaRecruiting
High River Community Cancer CentreHigh River, Alberta, CanadaNot Yet Recruiting
Central Alberta Cancer CentreRed Deer, Alberta, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT07024329