Informed consent may be seriously compromised if patients fail to understand the experimental nature of the trial in which they are participating. Using focus groups, the authors explored how prospective trial participants interpret and understand the science of clinical trials by using patient information sheets relative to their medical condition. An opportunity was provided to hear in the patients' own words how they interpret the information and why there is variable understanding. Respondents struggled to comprehend the meaning and purpose of concepts such as randomisation and double blinding, and found them threatening to their ideas of medical care. Suggestions are made about how to improve the national guidelines on written informat...
OBJECTIVE: Information on the rights of subjects in clinical trials has become increasingly complex ...
Objective: Information on the rights of subjects in clinical trials has become increasingly complex ...
Information on the rights of subjects in clinical trials has become increasingly complex and difficu...
Informed consent may be seriously compromised if patients fail to understand the experimental nature...
According to the Declaration of Helsinki, patients who take part in a clinical trial must be adequat...
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 ...
OBJECTIVE AND METHODS: A review conducted in 2005 identified many of the communication difficulties ...
There is increasing evidence that clinical trial participants are uninformed about the trials in whi...
The signed informed consent form provides documentary evidence that the patient has given informed c...
Informed consent is an essential element of research, and signing this document is required to condu...
We explored the comprehension of the informed consent in 77 cancer patients previously enrolled in r...
Background: Informed consent is a prerequisite for patients included in clinical trials. Trial desig...
Phase 1 (P1) trials are vital to the development of cancer treatments; however, the patients involve...
OBJECTIVE: Information on the rights of subjects in clinical trials has become increasingly complex ...
Objective: Information on the rights of subjects in clinical trials has become increasingly complex ...
Information on the rights of subjects in clinical trials has become increasingly complex and difficu...
Informed consent may be seriously compromised if patients fail to understand the experimental nature...
According to the Declaration of Helsinki, patients who take part in a clinical trial must be adequat...
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 ...
OBJECTIVE AND METHODS: A review conducted in 2005 identified many of the communication difficulties ...
There is increasing evidence that clinical trial participants are uninformed about the trials in whi...
The signed informed consent form provides documentary evidence that the patient has given informed c...
Informed consent is an essential element of research, and signing this document is required to condu...
We explored the comprehension of the informed consent in 77 cancer patients previously enrolled in r...
Background: Informed consent is a prerequisite for patients included in clinical trials. Trial desig...
Phase 1 (P1) trials are vital to the development of cancer treatments; however, the patients involve...
OBJECTIVE: Information on the rights of subjects in clinical trials has become increasingly complex ...
Objective: Information on the rights of subjects in clinical trials has become increasingly complex ...
Information on the rights of subjects in clinical trials has become increasingly complex and difficu...