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RECRUITING
NCT06351865

Feasibility Study to Evaluate the Use of Patient Reported Complications After Digital Consent

Sponsor: Portsmouth Hospitals NHS Trust

View on ClinicalTrials.gov

Summary

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.

Official title: A Feasibility Study to Evaluate if Breast Cancer Patients, Consented Using Digital Consent, Reliably Provide Accurate Patient Reported Complication (PRC) Data Using Feedback Questionnaires

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

50

Start Date

2024-03-07

Completion Date

2025-10-31

Last Updated

2025-07-17

Healthy Volunteers

No

Locations (1)

Queen Alexandra Hospital

Portsmouth, Hampshire, United Kingdom