Informed consent for clinical trials: a comparative study of standard versus simplified forms
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Innovating consent for pediatric HCT patientsEvidence-based patient choice: a prostate cancer decision aid in plain languageEasy-to-read informed consent forms for hematopoietic cell transplantation clinical trialsEthical considerations for informed consent in infertility research: The use of electronic health recordsRecruiting for epigenetic research: facilitating the informed consent processPre-counseling education for low literacy women at risk of Hereditary Breast and Ovarian Cancer (HBOC): patient experiences using the Cancer Risk Education Intervention Tool (CREdIT).Use of a modified informed consent process among vulnerable patients: a descriptive study.Linguistic Strategies for Improving Informed Consent in Clinical Trials Among Low Health Literacy Patients.Patients' perception of quality of pre-operative informed consent in athens, Greece: a pilot studyInforming potential participants about research: observational study with an embedded randomized controlled trial.Improving biobank consent comprehension: a national randomized survey to assess the effect of a simplified form and review/retest interventionMarginalized populations and drug addiction research: realism, mistrust, and misconceptionA randomized trial comparing concise and standard consent forms in the START trial.A need to simplify informed consent documents in cancer clinical trials. A position paper of the ARCAD Group.Informed consent document improvement does not increase patients' comprehension in biomedical research.An intervention to improve cancer patients' understanding of early-phase clinical trials.Variability among institutional review boards' decisions within the context of a multicenter trial.What potential research participants want to know about research: a systematic review.The HUNT study: participation is associated with survival and depends on socioeconomic status, diseases and symptomsAttitude towards informed consent practice in a developing country: a community-based assessment of the role of educational statusImproving understanding of clinical trial procedures among low literacy populations: an intervention within a microbicide trial in Malawi.The prevalence of limited health literacy.Interventions to improve health outcomes for patients with low literacy. A systematic review.Attitudes and beliefs of African Americans toward participation in medical research.Improving understanding in the research informed consent process: a systematic review of 54 interventions tested in randomized control trialsLost in translation: assessing effectiveness of focus group questioning techniques to develop improved translation of terminology used in HIV prevention clinical trials.Motivations, understanding, and voluntariness in international randomized trials.Subjects' expectations in neuroimaging research.Quality of communication in the ICU and surrogate's understanding of prognosis.Comprehensibility of translated informed consent documents used in clinical research in psychiatryReported consent processes and demographics: a substudy of the INSIGHT Strategic Timing of AntiRetroviral Treatment (START) trial.A pilot study of simple interventions to improve informed consent in clinical research: feasibility, approach, and resultsLength and complexity of US and international HIV consent forms from federal HIV network trials.Patient representatives' views on patient information in clinical cancer trials.Readability of patient education materials in ophthalmology: a single-institution study and systematic review.Randomization to standard and concise informed consent forms: development of evidence-based consent practicesImproved informed consent documents for biomedical research do not increase patients' understanding but reduce enrolment: a study in real settings.Informed consent in oncology clinical trials: A Brown University Oncology Research Group prospective cross-sectional pilot studyThe evaluation of the risks and benefits of phase II cancer clinical trials by institutional review board (IRB) members: a case study.Provider perceptions of limited health literacy in community health centers.
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P2860
Informed consent for clinical trials: a comparative study of standard versus simplified forms
description
article
@en
im Mai 1998 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в травні 1998
@uk
name
Informed consent for clinical ...... andard versus simplified forms
@en
Informed consent for clinical ...... andard versus simplified forms
@nl
type
label
Informed consent for clinical ...... andard versus simplified forms
@en
Informed consent for clinical ...... andard versus simplified forms
@nl
prefLabel
Informed consent for clinical ...... andard versus simplified forms
@en
Informed consent for clinical ...... andard versus simplified forms
@nl
P2093
P356
P1476
Informed consent for clinical ...... andard versus simplified forms
@en
P2093
H J Berkel
R F Holcombe
S G Divers
S Pramanik
P304
P356
10.1093/JNCI/90.9.668
P407
P577
1998-05-01T00:00:00Z