Add to ORKGThe issues discussed in this article emerged from a study that explored the decision-making processes used by research participants when deciding to participate in human subjects’ research. We discuss the current research and regulatory environment and its influences on participant decision-making. The results of this study create a framework for understanding the challenges of the current informed consent process and offers insights into what may be needed to create an environment that allows research participants to make more enlightened decisions
BACKGROUND: Despite widespread agreement on the importance of informed consent in clinical research,...
“Full disclosure is a necessary precondition to free choice. Accordingly, subjects who do not unders...
The process of informed consent is an ethical mandate for all clinical trials. The principles of eth...
The issues discussed in this article emerged from a study that explored the decision-making processe...
Background: Ethical problems most often arise in research. One of the most important ethical rules g...
Informed consent is important: in research, it allows subjects to make an informed and voluntary cho...
This article deals with the topic of social psychological research methods in practice, by examining...
Informed and voluntary consent are important aspects when conducting human research and is an area t...
Background: Informed consent, a critical enabler of clinical research, depends on the provision of r...
This article addresses two areas of continuing controversy about consent in clinical research: the q...
Providing informed consent to participate in research—a primary pillar of the ethical conduct of res...
INTRODUCTION: Participants and research professionals often overestimate how well participants under...
Participant – researcher communication during the informed consent process has characterized such in...
The current doctrine of informed consent falls far short of its potential to serve as a valuable saf...
There is increasing evidence that clinical trial participants are uninformed about the trials in whi...
BACKGROUND: Despite widespread agreement on the importance of informed consent in clinical research,...
“Full disclosure is a necessary precondition to free choice. Accordingly, subjects who do not unders...
The process of informed consent is an ethical mandate for all clinical trials. The principles of eth...
The issues discussed in this article emerged from a study that explored the decision-making processe...
Background: Ethical problems most often arise in research. One of the most important ethical rules g...
Informed consent is important: in research, it allows subjects to make an informed and voluntary cho...
This article deals with the topic of social psychological research methods in practice, by examining...
Informed and voluntary consent are important aspects when conducting human research and is an area t...
Background: Informed consent, a critical enabler of clinical research, depends on the provision of r...
This article addresses two areas of continuing controversy about consent in clinical research: the q...
Providing informed consent to participate in research—a primary pillar of the ethical conduct of res...
INTRODUCTION: Participants and research professionals often overestimate how well participants under...
Participant – researcher communication during the informed consent process has characterized such in...
The current doctrine of informed consent falls far short of its potential to serve as a valuable saf...
There is increasing evidence that clinical trial participants are uninformed about the trials in whi...
BACKGROUND: Despite widespread agreement on the importance of informed consent in clinical research,...
“Full disclosure is a necessary precondition to free choice. Accordingly, subjects who do not unders...
The process of informed consent is an ethical mandate for all clinical trials. The principles of eth...