Related references
Note: Only part of the references are listed.What Oncologists Believe They Said and What Patients Believe They Heard: An Analysis of Phase I Trial Discussions
Valerie Jenkins et al.
JOURNAL OF CLINICAL ONCOLOGY (2011)
Strategies for Increasing Recruitment to Randomised Controlled Trials: Systematic Review
Patrina H. Y. Caldwell et al.
PLOS MEDICINE (2010)
Key Principles to Guide Development of Consumer Medicine Information-Content Analysis of Information Design Texts
David K. Raynor et al.
ANNALS OF PHARMACOTHERAPY (2009)
Performance-based readability testing of participant materials for a phase I trial: TGN1412
P. Knapp et al.
JOURNAL OF MEDICAL ETHICS (2009)
Performance-based readability testing of participant information for a Phase 3 IVF trial
Peter Knapp et al.
TRIALS (2009)
Improvement of informed consent and the quality of consent documents
Michael Jefford et al.
LANCET ONCOLOGY (2008)
Recall of informed consent information by healthy volunteers in clinical trials
P. Fortun et al.
QJM-AN INTERNATIONAL JOURNAL OF MEDICINE (2008)
Long term clinical trials: How much information do participants retain from the informed consent process?
Joan M. Griffin et al.
CONTEMPORARY CLINICAL TRIALS (2006)
Communication and informed consent in phase 1 trials: a review of the literature
AC Cox et al.
SUPPORTIVE CARE IN CANCER (2006)
Assessing patient comprehension of informed consent forms
J Ancker
CONTROLLED CLINICAL TRIALS (2004)
Readability standards for informed-consent forms as compared with actual readability
MK Paasche-Orlow et al.
NEW ENGLAND JOURNAL OF MEDICINE (2003)