Background: Informed consent of trial participants is both an ethical and a legal requirement. When facing a decision about trial participation, potential participants are provided with information about the trial and have the opportunity to have any questions answered before their degree of ‘informed-ness’ is assessed, usually subjectively, and before they are asked to sign a consent form. Currently, standardised methods for assessing informed consent have tended to be focused on aspects of understanding and associated outcomes, rather than on the process of consent and the steps associated with decision-making. Methods: Potential trial participants who were approached regarding participation in one of three randomised controlled trials...
Abstract Background Informed consent (IC) is an ethical and legal prerequisite for trial participati...
Informed consent is an essential part of an ethical clinical trial; to this end, researchers have de...
BACKGROUND: Despite widespread agreement on the importance of informed consent in clinical research,...
Background: Informed consent of trial participants is both an ethical and a legal requirement. When ...
BACKGROUND: Informed consent of trial participants is both an ethical and a legal requirement. When ...
A study was conducted among participants in an antiretroviral therapy (ART) clinical trial to determ...
Informed consent (IC) is an ethical and legal prerequisite for trial participation, yet current appr...
There is increasing evidence that clinical trial participants are uninformed about the trials in whi...
Informed consent is an essential part of an ethical clinical trial; to this end, researchers have de...
Background: Research governance requires patients give informed consent to participate in clinical t...
Funding This research was supported by the MRC Methodology Fellowship (KG MR/L01193X/1. The Health S...
Funding: This work was supported by personal fellowship award (to KG - MR/L01193X/1) from the Medica...
IntroductionThe subjective assessment of the adequacy of informed consent for clinical trials, and t...
Abstract Background Evidence shows that the standard process for obtaining informed consent in clini...
Background Informed consent (IC) is an ethical and legal prerequisite for trial participation, yet c...
Abstract Background Informed consent (IC) is an ethical and legal prerequisite for trial participati...
Informed consent is an essential part of an ethical clinical trial; to this end, researchers have de...
BACKGROUND: Despite widespread agreement on the importance of informed consent in clinical research,...
Background: Informed consent of trial participants is both an ethical and a legal requirement. When ...
BACKGROUND: Informed consent of trial participants is both an ethical and a legal requirement. When ...
A study was conducted among participants in an antiretroviral therapy (ART) clinical trial to determ...
Informed consent (IC) is an ethical and legal prerequisite for trial participation, yet current appr...
There is increasing evidence that clinical trial participants are uninformed about the trials in whi...
Informed consent is an essential part of an ethical clinical trial; to this end, researchers have de...
Background: Research governance requires patients give informed consent to participate in clinical t...
Funding This research was supported by the MRC Methodology Fellowship (KG MR/L01193X/1. The Health S...
Funding: This work was supported by personal fellowship award (to KG - MR/L01193X/1) from the Medica...
IntroductionThe subjective assessment of the adequacy of informed consent for clinical trials, and t...
Abstract Background Evidence shows that the standard process for obtaining informed consent in clini...
Background Informed consent (IC) is an ethical and legal prerequisite for trial participation, yet c...
Abstract Background Informed consent (IC) is an ethical and legal prerequisite for trial participati...
Informed consent is an essential part of an ethical clinical trial; to this end, researchers have de...
BACKGROUND: Despite widespread agreement on the importance of informed consent in clinical research,...