The length of consent documents in oncological trials is doubled in twenty years.
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Easy-to-read informed consent forms for hematopoietic cell transplantation clinical trialsConsent and community engagement in diverse research contextsDo the patients read the informed consent?Ethical issues at the interface of clinical care and research practice in pediatric oncology: a narrative review of parents' and physicians' experiences.Repeated assessments of informed consent comprehension among HIV-infected participants of a three-year clinical trial in Botswana.A cross-cultural perspective on challenges facing comparative cancer survivorship research.Length and complexity of US and international HIV consent forms from federal HIV network trials.Temporal Trends and Predictors for Cancer Clinical Trial Availability for Medically Underserved Populations.Randomization to standard and concise informed consent forms: development of evidence-based consent practicesConsent timing and experience: modifiable factors that may influence interest in clinical researchInformed consent in oncology clinical trials: A Brown University Oncology Research Group prospective cross-sectional pilot studyAnalysis of informed consent document utilization in a minimal-risk genetic studyImproved participants' understanding in a healthy volunteer study using the SIDCER informed consent form: a randomized-controlled study.A randomized controlled trial of short and standard-length consent forms for a genetic cohort study: is longer better?Attitudes Toward Cancer Clinical Trial Participation in Young Adults with a History of Cancer and a Healthy College Student Sample: A Preliminary Investigation.Informed consent for phase I oncology trials: form, substance and signature.Is there an ethical obligation to disclose controversial risk? A question from the ACCORD Trial.Nationwide comprehensive gastro-intestinal cancer cohorts: the 3P initiative.Improved participants' understanding of research information in real settings using the SIDCER informed consent form: a randomized-controlled informed consent study nested with eight clinical trials.Satisfying the needs of Japanese cancer patients: a comparative study of detailed and standard informed consent documents.Views of clinical trial participants on the readability and their understanding of informed consent documents.Evidence-Based Strategies for Shortening Informed Consent Forms in Clinical Research.Readability of informed consent documents (1987-2007) for clinical trials: a linguistic analysisWhat information and the extent of information research participants need in informed consent forms: a multi-country surveyWhat Do Cancer Patients and Members of Ethical Review Boards in Norway Consider Important Elements of Informed Consent Documents?
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P2860
The length of consent documents in oncological trials is doubled in twenty years.
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2008 nî lūn-bûn
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2008年の論文
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2008年学术文章
@wuu
2008年学术文章
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2008年学术文章
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2008年学术文章
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2008年学术文章
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2008年学术文章
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2008年學術文章
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name
The length of consent documents in oncological trials is doubled in twenty years.
@en
The length of consent documents in oncological trials is doubled in twenty years.
@nl
type
label
The length of consent documents in oncological trials is doubled in twenty years.
@en
The length of consent documents in oncological trials is doubled in twenty years.
@nl
prefLabel
The length of consent documents in oncological trials is doubled in twenty years.
@en
The length of consent documents in oncological trials is doubled in twenty years.
@nl
P2093
P2860
P356
P1433
P1476
The length of consent documents in oncological trials is doubled in twenty years.
@en
P2093
P2860
P304
P356
10.1093/ANNONC/MDN623
P577
2008-10-15T00:00:00Z