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Study identifier: NCT07312786 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Testing the Feasibility of a Virtual Application to Support Breast and Colorectal Cancer Survivors

Condition: Breast Cancer Survivor · Colorectal Cancer Survivors  ·  Sponsor: Nova Scotia Health Authority

PhaseNA
Planned participants60
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this study is to determine the feasibility of implementing a mobile health application for breast and colorectal cancer survivors following primary treatment. Developed in collaboration with Seamless MD, the intervention acts as an information hub, providing users with timely and evidence-based information related to follow-up care as well as health system/community-based resources and programs to meet their needs during this period of care. The goal of the intervention is to encourage open communication regarding survivorship expectations and provide survivors with appropriate information and support to meet their needs. This study will: 1. Test the feasibility of implementing the virtual intervention at two cancer centres in Atlantic Canada (Nova Scotia and New Brunswick) 2. Gather feedback regarding the intervention from cancer survivors and healthcare providers. Participants will have access to the intervention for a period of six months. Questionnaires will be distributed to participants through the intervention at baseline, 90 days, and 180 days to assess user experience. Semi-structured interviews will be conducted with select survivor participants and healthcare providers (oncology and primary care) to determine the feasibility and acceptability of this intervention.

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

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Contact details are listed per location below or on the registry record.

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Locations (2)

Saint John Regional HospitalSaint John, New Brunswick, CanadaNot Yet Recruiting
Centre for Clinical Research QEII Health Sciences CentreHalifax, Nova Scotia, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT07312786