Successfully incorporating patient-reported outcomes (PROs) in clinical trials

Location
Centre for Professional Development – B1 on the Edgbaston Campus map
Category
Medical and Dental Sciences
Dates
Thursday 22nd (09:30) - Friday 23rd March 2018 (17:00)
Download the date to your calendar (.ics file)
Contact

Centre for Professional Development
Email: med-cpdbookings@contacts.bham.ac.uk

Learning Outcomes

  • Understand the different types of PROs and when to use them in clinical trials
  • Describe approaches to selecting an appropriate PRO measure for the study
  • Understand PRO-specific components that should be included in a trial protocol using the SPIRIT-PRO Extension
  • Appreciate approaches to minimise missing data and enhancing data quality
  • Understand the challenges and potential management strategies for PRO Alerts
  • Appreciate basic methods of PRO analysis 
  • Evaluate the reporting of a trial using the CONSORT-PRO extension
  • Consider ways to maximise the impact of PRO trial data to inform clinical practice and health-policy

Faculty


Professor Melanie Calvert, Professor of Outcomes Methodology, Director Centre for Patient Reported Outcomes Research
Dr Derek Kyte, NIHR Fellow, Deputy Director CPROR
Dr Anita Slade, Institute of Translational Medicine PROs Research Fellow
Dr Jonathan Bishop, Medical Statistician, Birmingham Clinical Trials Unit

Who is this course for?

This course is aimed at Chief and Principal Investigators, trial managers, clinical researchers, research nurses, data managers, study co-ordinators and academics.

Course Details

Duration
Two days

Location
Centre for Professional Development, Medical School, University of Birmingham

Fees
Registration: £295

How to apply 
Registration is now open, you can pay online using a credit or debit card here. If you have any questions regarding registration, please email the Medical Events Team at med-cpdbookings@contacts.bham.ac.uk.