Feasibility Study to Evaluate the Use of Patient Reported Complications After Digital Consent
Recruiting
Observational Study
Breast Cancer
Complication of Surgical Procedure
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Observational
- Participants needed
- 50 (estimated)
- Sponsor
- Portsmouth Hospitals NHS Trust · Government
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About This Trial
Patient report complication data to our best knowledge has not been studied yet in electronic consent. This study is a feasibility study to assess whether patients will reliably report their complications, the quality of this reporting and whether the information provided in the consent form matches up to their experience. This data will then be used to improve the consent process and evaluate whe…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Consent form 1- Adult patients who have the capacity to consent for themselves.
* Female adult aged 18years or above
* Diagnosed with early invasive breast cancer suitable for breast conserving surgery
* Undergoing Wide Local Excision of the breast and sentinel lymph node biop…
Contacts