Plain-English translation of NCT06351865 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Read our Breast Cancer research guide →This is a feasibility study testing whether breast cancer patients can accurately report their own complications and recovery experiences after breast surgery using a digital (online) consent and feedback system. Researchers want to understand whether patients will reliably share what side effects or problems they experience, and whether their real-world experiences match what doctors discussed with them before surgery.
Currently, doctors rely on their own records to track patient complications after surgery, but many problems may go unreported—especially as more patients manage their own follow-up care. By collecting this feedback directly from patients, the hospital hopes to get a fuller, more accurate picture of how surgery actually affects people, which could help improve the informed consent process and treatment decisions for future patients.
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You would consent to the study using a digital form that explains possible side effects from breast surgery. After your procedure, you would be asked to fill out questionnaires (either online or by phone) describing any complications or recovery issues you experience. The researchers would then compare what you report with the complications that were mentioned in your consent form to see whether the information matches your actual experience.
AI-generated summary from trial data · Sep 19, 2026 · Not medical advice
United Kingdom
Sponsor
Portsmouth Hospitals NHS Trust
Collaborators
University of East Anglia
Enrollment target
~50 participants
Started
March 2024
Primary completion
October 2027
Age range
18 Years and older
Sex
Female only
Last updated on clinicaltrials.gov in September 2026.
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Central contact
Ian Gedge
Portsmouth Hospitals NHS Trust
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