BACKGROUND: Informed consent is a requirement for all research. It is not, however, clear how much information is sufficient to make an informed decision about participation in research. Information on an online questionnaire about childhood development was provided through an unfolding electronic participant sheet in three levels of information. METHODS: 552 participants, who completed the web-based survey, accessed and spent time reading the participant information sheet (PIS) between July 2008 and November 2009. The information behaviour of the participants was investigated. The first level contained less information than might be found on a standard PIS, the second level corresponded to a standard PIS, and the third contained more infor...
Objectives To assess: 1) the feasibility of electronic information provision; 2) gather evidence on ...
This study aimed to investigate the effect of combined interventions composed of both quiz/feedback ...
OBJECTIVE: Information on the rights of subjects in clinical trials has become increasingly complex ...
BACKGROUND: Informed consent is a requirement for all research. It is not, however, clear how much i...
Background: Informed consent is a requirement for all research. It is not, however, clear how much i...
Background: The use of lengthy, detailed, and complex informed consent forms (ICFs) is of paramount ...
Background Informed consent in research is partly achieved through the use of information sheets. Th...
This PhD considered provision of information to potential research participants. It gathered data on...
To assess: 1) the feasibility of electronic information provision; 2) gather evidence on the topics ...
OBJECTIVES:To assess: 1) the feasibility of electronic information provision; 2) gather evidence on ...
This study was undertaken to measure potential research subjects’ participation in a survey research...
Abstract Background The process of informed consent for enrolment to a clinical research study can b...
There is increasing evidence that clinical trial participants are uninformed about the trials in whi...
Researchers typically attempt to fulfill disclosure and informed consent requirements by having part...
BACKGROUND: Despite widespread agreement on the importance of informed consent in clinical research,...
Objectives To assess: 1) the feasibility of electronic information provision; 2) gather evidence on ...
This study aimed to investigate the effect of combined interventions composed of both quiz/feedback ...
OBJECTIVE: Information on the rights of subjects in clinical trials has become increasingly complex ...
BACKGROUND: Informed consent is a requirement for all research. It is not, however, clear how much i...
Background: Informed consent is a requirement for all research. It is not, however, clear how much i...
Background: The use of lengthy, detailed, and complex informed consent forms (ICFs) is of paramount ...
Background Informed consent in research is partly achieved through the use of information sheets. Th...
This PhD considered provision of information to potential research participants. It gathered data on...
To assess: 1) the feasibility of electronic information provision; 2) gather evidence on the topics ...
OBJECTIVES:To assess: 1) the feasibility of electronic information provision; 2) gather evidence on ...
This study was undertaken to measure potential research subjects’ participation in a survey research...
Abstract Background The process of informed consent for enrolment to a clinical research study can b...
There is increasing evidence that clinical trial participants are uninformed about the trials in whi...
Researchers typically attempt to fulfill disclosure and informed consent requirements by having part...
BACKGROUND: Despite widespread agreement on the importance of informed consent in clinical research,...
Objectives To assess: 1) the feasibility of electronic information provision; 2) gather evidence on ...
This study aimed to investigate the effect of combined interventions composed of both quiz/feedback ...
OBJECTIVE: Information on the rights of subjects in clinical trials has become increasingly complex ...