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NCT07312786Recruiting

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

Testing the Feasibility of a Virtual Application to Support Breast and Colorectal Cancer Survivors After Completing Primary Treatment

Source: ClinicalTrials.gov · Last updated 14 May 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
24 Nov 2025
Start date
20 Apr 2026
Primary completion date
31 Dec 2026
Lead sponsor
Nova Scotia Health Authority
NCT number
NCT07312786

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From 20 Apr 2026 to the primary completion date, 31 Dec 2026
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Who the study is looking for

  • Adults older than 18 years, capable of providing informed consent
  • Diagnosed with stage I-III breast or colorectal cancer, and have completed primary treatment for their cancer (surgery and/or adjuvant systemic or radiation therapy) 6 months - 5 years ago

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Centre for Clinical Research QEII Health Sciences Centre
Coordinator of this site? Confirm its status
HalifaxCanadaRecruiting
Saint John Regional Hospital
Coordinator of this site? Confirm its status
Saint JohnCanadaNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.