Introduction: Pilot/feasibility studies assess the feasibility of conducting a larger study. Although researchers ought to communicate the feasibility objectives to their participants, many research ethics guidelines do not comment on how informed consent applies to pilot studies. It is unclear whether researchers and research ethics boards clearly communicate the purpose of pilot studies to participants consenting. The primary objective of this study is to assess whether pilot/feasibility studies submitted for ethics approval to a research ethics board transparently communicate the purpose of the study to participants through their informed consent practice. A highly transparent consent practice entails the consent documents communicate: ...
The regulatory guidelines on obtaining informed consent require that all protocols be reviewed by an...
There is increasing evidence that clinical trial participants are uninformed about the trials in whi...
Informed consent requires that potential clinical trial subjects be fully-informed and capable of ma...
INTRODUCTION: Pilot/feasibility studies assess the feasibility of conducting a larger study. Althoug...
Introduction Pilot/feasibility studies assess the feasibility of conducting a larger study. Although...
Abstract Background Pilot and feasibility studies (PA...
Funding: The authors have not declared a specific grant for this research from any funding agency in...
Acknowledgements The authors thank the Hamilton Integrated Research Ethics Board for facilitating th...
BACKGROUND: Pilot and feasibility studies (PAFS) often have complex objectives aimed at assessing fe...
Prior to a main randomized clinical trial, investigators often carry out a pilot or feasibility stud...
Background: Informed consent, a critical enabler of clinical research, depends on the provision of r...
Background: Ethical problems most often arise in research. One of the most important ethical rules g...
The process of informed consent is an ethical mandate for all clinical trials. The principles of eth...
Abstract Background The informed-consent process should be one of meaningful information exchange be...
Ethical and legal dogmas mandated obtaining informed consent from the research participants and thei...
The regulatory guidelines on obtaining informed consent require that all protocols be reviewed by an...
There is increasing evidence that clinical trial participants are uninformed about the trials in whi...
Informed consent requires that potential clinical trial subjects be fully-informed and capable of ma...
INTRODUCTION: Pilot/feasibility studies assess the feasibility of conducting a larger study. Althoug...
Introduction Pilot/feasibility studies assess the feasibility of conducting a larger study. Although...
Abstract Background Pilot and feasibility studies (PA...
Funding: The authors have not declared a specific grant for this research from any funding agency in...
Acknowledgements The authors thank the Hamilton Integrated Research Ethics Board for facilitating th...
BACKGROUND: Pilot and feasibility studies (PAFS) often have complex objectives aimed at assessing fe...
Prior to a main randomized clinical trial, investigators often carry out a pilot or feasibility stud...
Background: Informed consent, a critical enabler of clinical research, depends on the provision of r...
Background: Ethical problems most often arise in research. One of the most important ethical rules g...
The process of informed consent is an ethical mandate for all clinical trials. The principles of eth...
Abstract Background The informed-consent process should be one of meaningful information exchange be...
Ethical and legal dogmas mandated obtaining informed consent from the research participants and thei...
The regulatory guidelines on obtaining informed consent require that all protocols be reviewed by an...
There is increasing evidence that clinical trial participants are uninformed about the trials in whi...
Informed consent requires that potential clinical trial subjects be fully-informed and capable of ma...