Abstract Background Non-retention of participants seriously affects the credibility of clinical trial results and significantly reduces the potential of a trial to influence clinical practice. Non-retention can be defined as instances where participants leave the study prematurely. Examples include withdrawal of consent and loss to follow-up and thus outcome data cannot be obtained. The majority of existing interventions targeting retention fail to describe any theoretical basis for the observed improvement, or lack of improvement. Moreover, most of these interventions lack involvement of participants in their conception and/or design, raising questions about their relevance and acceptability. Many of the causes of non-retention involve peo...
Acknowledgements: The authors would like to thank Cynthia Fraser for her assistance in helping devel...
OBJECTIVE: To explore stakeholder perspectives upon participant retention in clinical trials, and to...
ObjectiveTo explore stakeholder perspectives upon participant retention in clinical trials, and to g...
Abstract Background Non-retention of participants seriously affects the credibility of clinical tria...
Background: Non-retention of participants seriously affects the credibility of clinical trial result...
Funding: This research is funded by the Chief Scientist Office of the Scottish Government’s Health a...
Abstract Background A failure of clinical trials to retain participa...
This research was supported by the Chief Scientist Office of the Scottish Government’s Health and So...
Abstract Background Randomised control trials are regarded as the gold standard for evaluating the e...
Background: Loss to follow-up from randomised trials can introduce bias and reduce study power, affe...
Abstract Background The failure to retain patients or collect primary-outcome data is a common chall...
Failing to retain an adequate number of study participants in behavioral intervention trials poses a...
Objective: To quantify the effect of strategies to improve retention in randomised trials.<p></p> ...
Abstract Background Loss to follow-up (attrition) is a frequent problem in clinical trials and can i...
Background One of the top three research priorities for the UK clinical trial community is to addres...
Acknowledgements: The authors would like to thank Cynthia Fraser for her assistance in helping devel...
OBJECTIVE: To explore stakeholder perspectives upon participant retention in clinical trials, and to...
ObjectiveTo explore stakeholder perspectives upon participant retention in clinical trials, and to g...
Abstract Background Non-retention of participants seriously affects the credibility of clinical tria...
Background: Non-retention of participants seriously affects the credibility of clinical trial result...
Funding: This research is funded by the Chief Scientist Office of the Scottish Government’s Health a...
Abstract Background A failure of clinical trials to retain participa...
This research was supported by the Chief Scientist Office of the Scottish Government’s Health and So...
Abstract Background Randomised control trials are regarded as the gold standard for evaluating the e...
Background: Loss to follow-up from randomised trials can introduce bias and reduce study power, affe...
Abstract Background The failure to retain patients or collect primary-outcome data is a common chall...
Failing to retain an adequate number of study participants in behavioral intervention trials poses a...
Objective: To quantify the effect of strategies to improve retention in randomised trials.<p></p> ...
Abstract Background Loss to follow-up (attrition) is a frequent problem in clinical trials and can i...
Background One of the top three research priorities for the UK clinical trial community is to addres...
Acknowledgements: The authors would like to thank Cynthia Fraser for her assistance in helping devel...
OBJECTIVE: To explore stakeholder perspectives upon participant retention in clinical trials, and to...
ObjectiveTo explore stakeholder perspectives upon participant retention in clinical trials, and to g...