Feasibility Study to Evaluate the Use of Patient Reported Complications After Digital Consent
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorPortsmouth Hospitals NHS Trust
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 whether the Patient Initiated Follow Up (PIFU) model is effective or if it leads to underreporting of problems.
Eligibility criteria
Qualifiers
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.
Disqualifiers
Unable to consent for themselves or do not wish to participate.
Patients who need an interpreter.
Trial design
Treatments tested in this trial
- Not listed
Trial groups
No trial groups listed
Sponsors and collaborators
Portsmouth Hospitals NHS Trust
Lead sponsor
University of East Anglia
Collaborator
Source ClinicalTrials.gov