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Easy-to-read informed consent forms for hematopoietic cell transplantation clinical trialsReadability and Content Assessment of Informed Consent Forms for Phase II-IV Clinical Trials in ChinaEmerging issues in paediatric health research consent forms in Canada: working towards best practicesQualitative thematic analysis of consent forms used in cancer genome sequencingComparison of participant information and informed consent forms of five European studies in genetic isolated populationsHealth Interoperability into Practice: Results of the Development of a Consent Form in a Pilot Project in a Health District in São Paulo, Brazil.[Revision of the informed consent form for patients based on investigation of adverse events of mFOLFOX6 regimen].Screening the use of informed consent forms prior to procedures involving operative dentistry: ethical aspects.The readability of information and consent forms in clinical research in France.A randomized trial comparing concise and standard consent forms in the START trial.Evaluating the quality of information about alternatives to research participation in oncology consent forms.Developing a simplified consent form for biobanking.How can an IRB avoid the use of obsolete consent forms?Are research participants truly informed? Readability of informed consent forms used in research.The definition of placebo in the informed consent forms of clinical trials.Assessing the adequacy of procedure-specific consent forms in orthopaedic surgery against current methods of operative consent.The ethics of HIV "cure" research: what can we learn from consent forms?Readability standards for informed-consent forms as compared with actual readability.Assessing the readability of non-English-language consent forms: the case of Kiswahili for research conducted in Kenya.Disclosure of the right of research participants to receive research results: an analysis of consent forms in the Children's Oncology Group.GCP compliance and readability of informed consent forms from an emerging hub for clinical trials.Therapeutic optimism in the consent forms of phase 1 gene transfer trials: an empirical analysisLength and complexity of US and international HIV consent forms from federal HIV network trials.Institutional Review Board (IRB) review lacks impact on the readability of consent forms for research.Instructions and consent forms for allergen immunotherapy.Readability and Content Assessment of Informed Consent Forms for Medical Procedures in CroatiaAre patient consent forms for research protocols easy to read?Do written consent forms provide medicolegal protection from litigation in radiotherapy?The new consent form: is it any better?Recommendations for informed consent forms for critical care clinical trials.Randomization to standard and concise informed consent forms: development of evidence-based consent practicesDo surgeons and patients discuss what they document on consent forms?Review by a local medical research ethics committee of the conduct of approved research projects, by examination of patients' case notes, consent forms, and research records and by interviewThe Appropriateness of Language Found in Research Consent Form Templates: A Computational Linguistic AnalysisInforming egg donors of the potential for embryonic research: a survey of consent forms from U.S. in vitro fertilization clinics.Ethical issues arising from the requirement to sign a consent form in palliative careImproved participants' understanding in a healthy volunteer study using the SIDCER informed consent form: a randomized-controlled study.Do characteristics of HIPAA consent forms affect the response rate?Comprehension and informed consent: assessing the effect of a short consent form.VICO: Ontology-based representation and integrative analysis of Vaccination Informed Consent forms
P921
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P921
description
form used to document informed consent
@en
name
formularo pri informita konsento
@eo
informed consent form
@en
type
label
formularo pri informita konsento
@eo
informed consent form
@en
prefLabel
formularo pri informita konsento
@eo
informed consent form
@en