PNG version of QUB Shield - Red

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Workflow of study

Workflow of study

  1. The data collection proforma will be designed by IT staff under supervision of clinicians, with suggestions from TVOs and statistician.
  2. The proforma will be piloted by TVOs, and its design will be reviewed and necessary adjustments incorporated.
  3. Medical records staff will pull the charts of the bladder cancer patients for the TVOs to collect data in proforma.
  4. On completion of the data collection, the data will be cleaned and prepared for analysis by statistician.
  5. The data will be analysed and the results written into a report by statistician.
  6. Consultant urologists will be given an opportunity to comment on draft report, and advise on relevancy of reported results.
  7. Report and recommendations will be produced, published and disseminated.