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

ECTU PROMiSe study logo

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

This article was published on