REPORT-UK: Phase 3 Pilot study (Version 1)

• Research type

  Research Study

• Full title

  Real-time Electronic Patient Outcome ReporTing of adverse events in UK (REPORT-UK): Phase 3 Pilot study

• IRAS ID

  150873

• Contact name

  Galina Velikova

• Contact email

  g.velikova@leeds.ac.uk

• Research summary

  This study is a phase III pilot study which aims to evaluate feasibility and patient compliance with using an internet-based or telephone-based system for collecting patient-reported adverse event (AE) data and other patient-reported outcome measures (PROMs) by measuring recruitment rate, attrition over time and proportion of missing data. The study will also report the proportion of weekly adverse event reports completed.

• REC name

  Yorkshire & The Humber - Leeds East Research Ethics Committee

• REC reference

  14/YH/0181

• Date of REC Opinion

  18 Jun 2014

• REC opinion

  Further Information Favourable Opinion