Improvement of informed consent and the quality of consent documents.
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A review of approaches to improve participation of culturally and linguistically diverse populations in clinical trialsInformed consent comprehension in African research settingsInformed consent: do information pamphlets improve post-operative risk-recall in patients undergoing total thyroidectomy: prospective randomized control study.Practice variation across consent templates for biobank research. a survey of German biobanksDo informed consent documents for cancer trials do what they should? A study of manifest and latent functionsRecruiting for epigenetic research: facilitating the informed consent processInformed consent conversations and documents: A quantitative comparison.Patient reactions to confidentiality, liability, and financial aspects of informed consent in cardiology researchConsent, including advanced consent, of older adults to research in care homes: a qualitative study of stakeholders' views in South Wales.A survey of the current practice of the informed consent process in general surgery in the NetherlandsEvaluating the quality of informed consent and contemporary clinical practices by medical doctors in South Africa: an empirical studyPotential bias in the bank: what distinguishes refusers, nonresponders and participants in a clinic-based biobank?A European study on alcohol and drug use among young drivers: the TEND by Night study design and methodology.Risk communication in clinical trials: a cognitive experiment and a surveyBringing a humanistic approach to cancer clinical trials.Informed consent prior to coronary angiography in a real world scenario: what do patients remember?Improving decision making about clinical trial participation - a randomised controlled trial of a decision aid for women considering participation in the IBIS-II breast cancer prevention trial.Incidental computer tomography radiologic findings through research participation in the North Texas Healthy Heart Study.Can user testing of a clinical trial patient information sheet make it fit-for-purpose?--a randomized controlled trial.Theoretical model of critical issues in informed consent in HIV vaccine trialsRepeated assessments of informed consent comprehension among HIV-infected participants of a three-year clinical trial in Botswana.Consent for use of clinical leftover biosample: a survey among Chinese patients and the general publicPatient- and provider-reported information about transplantation and subsequent waitlistingThe definition of placebo in the informed consent forms of clinical trials.Communication training for advanced medical students improves information recall of medical laypersons in simulated informed consent talks--a randomized controlled trial.Parent perspectives on consent for the linkage of data to evaluate vaccine safety: a randomised trial of opt-in and opt-out consent.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.Pilot study demonstrating effectiveness of targeted education to improve informed consent understanding in AIDS clinical trials.Addressing risks to advance mental health research.When a serious adverse event in research occurs, how do other volunteers react?Evaluation of an educational program to improve communication with patients about early-phase trial participationAchieving new levels of recall in consent to research by combining remedial and motivational techniques.Patient representatives' views on patient information in clinical cancer trials.The Development of a Communication Tool to Facilitate the Cancer Trial Recruitment Process and Increase Research Literacy among Underrepresented Populations.Unraveling preimplantation genetic diagnosis for high-risk couples: implications for nurses at the front line of care.Informed consent in oncology clinical trials: A Brown University Oncology Research Group prospective cross-sectional pilot studyMolecular Tumor Boards: Ethical Issues in the New Era of Data Medicine.The coordination of primary and oncology specialty care at the end of life.Clinical practice guidelines of the French Association for Supportive Care in Cancer and the French Society for Psycho-oncology: refusal of treatment by adults afflicted with cancer.
P2860
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P2860
Improvement of informed consent and the quality of consent documents.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on May 2008
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Improvement of informed consent and the quality of consent documents.
@en
Improvement of informed consent and the quality of consent documents.
@nl
type
label
Improvement of informed consent and the quality of consent documents.
@en
Improvement of informed consent and the quality of consent documents.
@nl
prefLabel
Improvement of informed consent and the quality of consent documents.
@en
Improvement of informed consent and the quality of consent documents.
@nl
P1433
P1476
Improvement of informed consent and the quality of consent documents.
@en
P2093
Rosemary Moore
P304
P356
10.1016/S1470-2045(08)70128-1
P50
P577
2008-05-01T00:00:00Z