Long term clinical trials: how much information do participants retain from the informed consent process?
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Readability and Content Assessment of Informed Consent Forms for Phase II-IV Clinical Trials in ChinaCan user testing of a clinical trial patient information sheet make it fit-for-purpose?--a randomized controlled trial.Subjects agree to participate in environmental health studies without fully comprehending the associated riskParticipants' understanding of informed consent in clinical trials over three decades: systematic review and meta-analysis.Patient representatives' views on patient information in clinical cancer trials.Appreciation of the informed consent procedure in a randomised trial of decompressive surgery for space occupying hemispheric infarction.Performance-based readability testing of participant information for a Phase 3 IVF trial.Assessing and improving research participants' understanding of risk: potential lessons from the literature on physician-patient risk communication.Patient information leaflets (PILs) for UK randomised controlled trials: a feasibility study exploring whether they contain information to support decision making about trial participation.Investigating the informed consent process, therapeutic misconception and motivations of Egyptian research participants: a qualitative pilot study.Remote preenrollment checking of consent forms to reduce nonconformity.Towards optimised information about clinical trials; identification and validation of key issues in collaboration with cancer patient advocates.Two methods of obtaining informed consent in a genetic epidemiological study: effects on understandingThe Understanding of Informed Consent Information—Definitions and Measurements in Empirical StudiesThe effect of optimised patient information materials on recruitment in a lung cancer screening trial: an embedded randomised recruitment trial
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P2860
Long term clinical trials: how much information do participants retain from the informed consent process?
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2006 nî lūn-bûn
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2006年の論文
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2006年学术文章
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2006年学术文章
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2006年学术文章
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2006年学术文章
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name
Long term clinical trials: how ...... the informed consent process?
@en
Long term clinical trials: how ...... the informed consent process?
@nl
type
label
Long term clinical trials: how ...... the informed consent process?
@en
Long term clinical trials: how ...... the informed consent process?
@nl
prefLabel
Long term clinical trials: how ...... the informed consent process?
@en
Long term clinical trials: how ...... the informed consent process?
@nl
P2093
P1476
Long term clinical trials: how ...... the informed consent process?
@en
P2093
David B Nelson
Dorothea Collins
James K Struve
Joan M Griffin
P304
P356
10.1016/J.CCT.2006.04.006
P407
P577
2006-05-12T00:00:00Z