Acknowledgements This work was supported by personal fellowship award (to KG) from the Medical Research Council’s Strategic Skills Methodology programme. The Health Services Research Unit is supported by a core grant from the Chief Scientist Office of the Scottish Government Health and Social Care Directorates. PW is funded by a UK Medical Research Council Hub for Trials Methodology Research Network grant G0800792. The views and opinions expressed therein are those of the authors and do not necessarily reflect those of the Chief Scientist Office, MRC or the Department of Health.Peer reviewedPublisher PD
Abstract Background Recent evidence has highlighted d...
Acknowledgements We would like to thank the lay advisory group who provide invaluable insight and su...
PURPOSES: This research set out to contribute to ongoing efforts to improve the quality of informed ...
ObjectiveTo develop a core outcome set for the evaluation of interventions that aim to improve how p...
Funding: This work was supported by personal fellowship award (to KG - MR/L01193X/1) from the Medica...
of interventions for informed consent for randomised controlled trials (ELICIT): protocol for a syst...
Abstract Background The concept of informed consent is fundamental to medical practice. Shortcomings...
Background Trials involving adults who lack capacity to provide consent rely on proxy or surrogat...
AbstractEthically sound clinical research requires that prospective study participants provide volun...
Objectives: To develop a conceptual framework of preferences for interventions in the context of ran...
IntroductionThe subjective assessment of the adequacy of informed consent for clinical trials, and t...
Background: Randomised trials play a vital role in underpinning evidence-based care. However, trials...
Informed consent (IC) is an ethical and legal prerequisite for trial participation, yet current appr...
Background: Informed consent of trial participants is both an ethical and a legal requirement. When ...
Introduction Early phase cancer clinical trials have become increasingly complicated in terms of pat...
Abstract Background Recent evidence has highlighted d...
Acknowledgements We would like to thank the lay advisory group who provide invaluable insight and su...
PURPOSES: This research set out to contribute to ongoing efforts to improve the quality of informed ...
ObjectiveTo develop a core outcome set for the evaluation of interventions that aim to improve how p...
Funding: This work was supported by personal fellowship award (to KG - MR/L01193X/1) from the Medica...
of interventions for informed consent for randomised controlled trials (ELICIT): protocol for a syst...
Abstract Background The concept of informed consent is fundamental to medical practice. Shortcomings...
Background Trials involving adults who lack capacity to provide consent rely on proxy or surrogat...
AbstractEthically sound clinical research requires that prospective study participants provide volun...
Objectives: To develop a conceptual framework of preferences for interventions in the context of ran...
IntroductionThe subjective assessment of the adequacy of informed consent for clinical trials, and t...
Background: Randomised trials play a vital role in underpinning evidence-based care. However, trials...
Informed consent (IC) is an ethical and legal prerequisite for trial participation, yet current appr...
Background: Informed consent of trial participants is both an ethical and a legal requirement. When ...
Introduction Early phase cancer clinical trials have become increasingly complicated in terms of pat...
Abstract Background Recent evidence has highlighted d...
Acknowledgements We would like to thank the lay advisory group who provide invaluable insight and su...
PURPOSES: This research set out to contribute to ongoing efforts to improve the quality of informed ...