PROMiSe
Patient Reported Outcome MeasureS using Electronic informed consent and data capture – developing methods and infrastructure
Patients taking part in research will often be asked to complete ‘Quality of Life’ questionnaires in person or by post to record how they are feeling. The PROMiSe team are creating a website which provides information for the patient, a consent form and questionnaires so everything can be completed online at home. The trial involves asking around 100 Patient and Public Involvement (PPI) volunteers to help test if this system works well and is easy to use by asking them to complete 2 short questionnaires, once a month for 6 months and provide feedback. If it proves to be simple to use, the aim would be to use this system in future research projects.
Chief Investigator: Professor Sandra Eldridge (Barts and the London Pragmatic Clinical Trials Unit)
Number and location of participating sites / geographical scope (by region/ country): PROMiSe is a collaboration between the Pragmatic Clinical Trials Unit (PCTU), Edinburgh Clinical Trials Unit (ECTU) and Birmingham Clinical Trials Unit (BCTU).
Funder: National Institute for Health Research- CTU Support Funding programme
Start and End date
Of grant award: 31/08/2017 – 31/08/2018
Of recruitment
Current Status: in recruitment
UK GDPR privacy statement: https://www.qmul.ac.uk/site/privacy/
Sponsor: Queen Mary, University of London
Chief Investigator: Professor Sandra Eldridge, Director, Pragmatic Clinical Trials Unit, Barts and the London Pragmatic Clinical Trials Unit, Yvonne Carter Building, 58 Turner St, Whitechapel, E12AB; Tel: 0207 882 2519; Email: s.eldridge@qmul.ac.uk
Trial Management: Natasha Stevens (PCTU)
PCTU: Shiva Taheri
ECTU: Kat Oatey
BCTU: Laura Magill, Sarah Marium Khan
ECTU Involvement: Trial management / Statistics