Background One of the top three research priorities for the UK clinical trial community is to address the gap in evidence-based approaches to improving participant retention in randomised trials. Despite this, there is little evidence supporting methods to improve retention. This paper reports the PRioRiTy II project, a Priority Setting Partnership (PSP) that identified and prioritised unanswered questions and uncertainties around trial retention in collaboration with key stakeholders. Methods This PSP was conducted in collaboration with the James Lind Alliance, a non-profit making initiative, to support key stakeholders (researchers, patients, and the public) in jointly identifying and agreeing on priority research questions. There were th...
Acknowledgements The authors would like to acknowledge those who provided information regarding the ...
Funding: This research is funded by the Chief Scientist Office of the Scottish Government’s Health a...
Funding The author(s) disclosed receipt of the following financial support for the research, authors...
Background One of the top three research priorities for the UK clinical trial community is to addres...
Acknowledgements The authors would like to thank all stakeholders who took part, all respondents to ...
Despite the problem of inadequate recruitment to randomised trials, there is little evidence to guid...
Background: Despite the problem of inadequate recruitment to randomised trials, there is little evid...
peer-reviewedBackground: Despite the problem of inadequate recruitment to randomised trials, there i...
Background: Despite the problem of inadequate recruitment to randomised trials, there is little evid...
Acknowledgements The authors would like to thank all contributing individuals who completed the surv...
Abstract Background Despite the problem of inadequate recruitment to randomised trials, there is lit...
Abstract Background The failure to retain patients or collect primary-outcome data is a common chall...
Background Non-retention of participants seriously affects the credibility of clinical trial result...
Background: Non-retention of participants seriously affects the credibility of clinical trial result...
Background: Loss to follow-up from randomised trials can introduce bias and reduce study power, affe...
Acknowledgements The authors would like to acknowledge those who provided information regarding the ...
Funding: This research is funded by the Chief Scientist Office of the Scottish Government’s Health a...
Funding The author(s) disclosed receipt of the following financial support for the research, authors...
Background One of the top three research priorities for the UK clinical trial community is to addres...
Acknowledgements The authors would like to thank all stakeholders who took part, all respondents to ...
Despite the problem of inadequate recruitment to randomised trials, there is little evidence to guid...
Background: Despite the problem of inadequate recruitment to randomised trials, there is little evid...
peer-reviewedBackground: Despite the problem of inadequate recruitment to randomised trials, there i...
Background: Despite the problem of inadequate recruitment to randomised trials, there is little evid...
Acknowledgements The authors would like to thank all contributing individuals who completed the surv...
Abstract Background Despite the problem of inadequate recruitment to randomised trials, there is lit...
Abstract Background The failure to retain patients or collect primary-outcome data is a common chall...
Background Non-retention of participants seriously affects the credibility of clinical trial result...
Background: Non-retention of participants seriously affects the credibility of clinical trial result...
Background: Loss to follow-up from randomised trials can introduce bias and reduce study power, affe...
Acknowledgements The authors would like to acknowledge those who provided information regarding the ...
Funding: This research is funded by the Chief Scientist Office of the Scottish Government’s Health a...
Funding The author(s) disclosed receipt of the following financial support for the research, authors...