Acknowledgements The authors would like to thank all interviewees that took part in this study, as well as our colleagues and fellow members of the Trial Forge, HRB-TMRN, and MRC Trial Methodology Hubs networks that supported in identifying potential participants. Funding This project was funded by the Chief Scientist Office, grant number HIPS/18/04Peer reviewedPublisher PD
Background Patient-reported outcomes (PROs) are increasingly collected in clinical trials as they p...
OBJECTIVES: To identify factors associated with good and poor recruitment to multicentre trials. DAT...
BACKGROUND Patient-reported outcomes (PROs) are increasingly collected in clinical trials as they...
Abstract Introduction Selecting and collecting data to support appropriate primary and secondary out...
Objectives: To provide information on the frequency and reasons for outcome reporting bias in clinic...
OBJECTIVES: To provide information on the frequency and reasons for outcome reporting bias in clinic...
Acknowledgements The authors would like to thank Rumana Newlands (RN) for her work in conducting the...
Acknowledgments We would like to thank all of the participants who volunteered and gave up their tim...
Purpose: Evidence suggests that the patient-reported outcome (PRO) content of cancer trial protocol...
Background: There is an ethical imperative to offer the results of trials to those who participated....
BackgroundCore outcome sets (COS) are standardised sets of outcomes, which represent the minimum out...
BACKGROUND: There is an ethical imperative to offer the results of trials to those who participated....
Aims: The aim of the study was to identify actionable learning points from stakeholders in remote de...
Acknowledgements We would like to thank all of the participants who volunteered their time to contri...
Abstract Purpose: Evidence suggests that the patient- reported outcome (PRO) content of cancer tria...
Background Patient-reported outcomes (PROs) are increasingly collected in clinical trials as they p...
OBJECTIVES: To identify factors associated with good and poor recruitment to multicentre trials. DAT...
BACKGROUND Patient-reported outcomes (PROs) are increasingly collected in clinical trials as they...
Abstract Introduction Selecting and collecting data to support appropriate primary and secondary out...
Objectives: To provide information on the frequency and reasons for outcome reporting bias in clinic...
OBJECTIVES: To provide information on the frequency and reasons for outcome reporting bias in clinic...
Acknowledgements The authors would like to thank Rumana Newlands (RN) for her work in conducting the...
Acknowledgments We would like to thank all of the participants who volunteered and gave up their tim...
Purpose: Evidence suggests that the patient-reported outcome (PRO) content of cancer trial protocol...
Background: There is an ethical imperative to offer the results of trials to those who participated....
BackgroundCore outcome sets (COS) are standardised sets of outcomes, which represent the minimum out...
BACKGROUND: There is an ethical imperative to offer the results of trials to those who participated....
Aims: The aim of the study was to identify actionable learning points from stakeholders in remote de...
Acknowledgements We would like to thank all of the participants who volunteered their time to contri...
Abstract Purpose: Evidence suggests that the patient- reported outcome (PRO) content of cancer tria...
Background Patient-reported outcomes (PROs) are increasingly collected in clinical trials as they p...
OBJECTIVES: To identify factors associated with good and poor recruitment to multicentre trials. DAT...
BACKGROUND Patient-reported outcomes (PROs) are increasingly collected in clinical trials as they...