To assess: 1) the feasibility of electronic information provision; 2) gather evidence on the topics and level of detail of information potential research participant’s accessed; 3) to assess satisfaction and understanding.Observational study with an embedded randomised controlled trial.Low risk intervention study based in primary care.White British & Irish, South Asian and African-Caribbean subjects aged between 40-74 years eligible for a blood pressure monitoring study.PDF copy of the standard paper participant information sheet (PDF-PIS) and an electronic Interactive Information Sheet (IIS) where participants could choose both the type and level of detail accessed.1) Proportion of participants providing an email address and accessing elec...
Background: Informed consent is a requirement for all research. It is not, however, clear how much i...
BACKGROUND: Informed consent is a critical component of clinical research. Different methods of pres...
BACKGROUND: Informed consent is a requirement for all research. It is not, however, clear how much i...
OBJECTIVES:To assess: 1) the feasibility of electronic information provision; 2) gather evidence on ...
Objectives To assess: 1) the feasibility of electronic information provision; 2) gather evidence on ...
<div><p>Objectives</p><p>To assess: 1) the feasibility of electronic information provision; 2) gathe...
Objectives To assess: 1) the feasibility of electronic information provision; 2) gather evidence ...
This PhD considered provision of information to potential research participants. It gathered data on...
Objective: To assess the efficacy, with respect to participant understanding of information, of a co...
There is increasing evidence that clinical trial participants are uninformed about the trials in whi...
Background: Patient understanding of study information is fundamental to gaining informed consent to...
Objective: To determine the preferred means by which participants in a study of cardiac rehabilitati...
There is increasing evidence that clinical trial participants are uninformed about the trials in whi...
It is both an ethical and a legal requirement that patients who participate in clinical trials must ...
Background: Informed consent is a requirement for all research. It is not, however, clear how much i...
BACKGROUND: Informed consent is a critical component of clinical research. Different methods of pres...
BACKGROUND: Informed consent is a requirement for all research. It is not, however, clear how much i...
OBJECTIVES:To assess: 1) the feasibility of electronic information provision; 2) gather evidence on ...
Objectives To assess: 1) the feasibility of electronic information provision; 2) gather evidence on ...
<div><p>Objectives</p><p>To assess: 1) the feasibility of electronic information provision; 2) gathe...
Objectives To assess: 1) the feasibility of electronic information provision; 2) gather evidence ...
This PhD considered provision of information to potential research participants. It gathered data on...
Objective: To assess the efficacy, with respect to participant understanding of information, of a co...
There is increasing evidence that clinical trial participants are uninformed about the trials in whi...
Background: Patient understanding of study information is fundamental to gaining informed consent to...
Objective: To determine the preferred means by which participants in a study of cardiac rehabilitati...
There is increasing evidence that clinical trial participants are uninformed about the trials in whi...
It is both an ethical and a legal requirement that patients who participate in clinical trials must ...
Background: Informed consent is a requirement for all research. It is not, however, clear how much i...
BACKGROUND: Informed consent is a critical component of clinical research. Different methods of pres...
BACKGROUND: Informed consent is a requirement for all research. It is not, however, clear how much i...