Feasibility Study to Evaluate the Use of Patient Reported Complications After Digital Consent
About this study
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 whether the Patient Initiated Follow Up (PIFU) model is effective or if it leads to underreporting of problems.
- Condition
- Breast Cancer, Complication of Surgical Procedure
- Sponsor
- Portsmouth Hospitals NHS Trust
Who can join
- Age
- 18 years and older
- Sex
- Female only
- Healthy volunteers
- Not accepted
Inclusion 9
- Minimum age: 18 years
- Eligible sex: Female
- Study condition: Breast Cancer, Complication of Surgical Procedure
- 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 biopsy.
- Participant must be able to fill out an electronic questionnaire or take part in a phone questionnaire.
- Participant is willing and able to give informed consent for participation in the study.
Exclusion 2
- Unable to consent for themselves or do not wish to participate.
- Patients who need an interpreter.
Where
1 site, 1 recruiting
Queen Alexandra Hospital
Portsmouth, Hampshire, United Kingdom
Contact
-
Ian Gedge
02392286000 ian.gedge@porthosp.nhs.uk
Potential match only. Final eligibility is determined by the study team.