Ethics committees bear a responsibility for patient information. Informed consent implies that the patient understands what he has consented to
L Werkö - Lakartidningen, 2002 - europepmc.org
A cornerstone in health care is the duty to inform patients not only of their right to partake in
decisions about their care but also of the various options for treatment. This applies …
decisions about their care but also of the various options for treatment. This applies …
[HTML][HTML] Informed consent in oncology clinical trials: A Brown University Oncology Research Group prospective cross-sectional pilot study
A Schumacher, WM Sikov, MI Quesenberry, H Safran… - PLoS …, 2017 - journals.plos.org
Background Informed consent forms (ICFs) for oncology clinical trials have grown
increasingly longer and more complex. We evaluated objective understanding of critical …
increasingly longer and more complex. We evaluated objective understanding of critical …
A survey on the cognition on informed consent for clinical trials of cancer treating personnel
H Moon, HK Kim - Journal of Korean Society for Clinical Pharmacology …, 2000 - tcpharm.org
Background Investigators presented a survey of the cognition on clnical trial and informed
consent of cancer patients and their family (Korean J Clin Pharmacol Ther 3: 141–153 …
consent of cancer patients and their family (Korean J Clin Pharmacol Ther 3: 141–153 …
[PDF][PDF] SIDCER informed consent form: principles and a developmental guideline
N Koonrungsesomboon, J Laothavorn… - Indian J Med …, 2016 - academia.edu
The quality of informed consent forms (ICFs) remains an issue in clinical research. The
lengthy and complicated ICFs currently being used lower research participants' ability to …
lengthy and complicated ICFs currently being used lower research participants' ability to …
[HTML][HTML] Improving oncology first-in-human and Window of opportunity informed consent forms through participant feedback
AM Avinger, HC Sibold, G Campbell, E Abernethy… - BMC medical …, 2023 - Springer
Background Although patient advocates have developed templates for standard consent
forms, evaluating patient preferences for first in human (FIH) and window of opportunity …
forms, evaluating patient preferences for first in human (FIH) and window of opportunity …
Will shorter informed consent forms with visual aids improve understanding of the document in adult and elderly populations of clinical trials?
A Bloswick, A Skowron - Ethics & Medicine, 2019 - search.proquest.com
The informed consent form (ICF) is a critical document for ensuring patients are properly
informed about participation in clinical trials, yet there are no regulations that govern the …
informed about participation in clinical trials, yet there are no regulations that govern the …
Analysis of patient information leaflets (PILs), used in clinical trials using the Informed Consent Evaluation instrument (ICEi)
K Gillies, W Huang, Z Skea, S Cotton - Trials, 2011 - Springer
Background Informed consent (IC) is regarded as a cornerstone of ethical healthcare
research and is a requirement for most clinical research studies [1]. Guidelines suggest that …
research and is a requirement for most clinical research studies [1]. Guidelines suggest that …
[HTML][HTML] 1856P Electronic informed consent: The need to redesign the consent process for the digital era
C Cagnazzo, O Nanni, A Di Costanzo… - Annals of …, 2021 - annalsofoncology.org
Background The Electronic Informed Consent (eIC) was introduced with the aim of
optimizing time and costs, providing the essential characteristics of a clinical study in an …
optimizing time and costs, providing the essential characteristics of a clinical study in an …
A comparison of the quality of informed consent for phase I oncology trials over a 30-year period
L Malik, J Cooper - Cancer Chemotherapy and Pharmacology, 2018 - Springer
Purpose Efforts are underway in improving the informed consent process. The success of
these efforts to improve quality of informed consent forms (ICFs) for phase I oncology trials …
these efforts to improve quality of informed consent forms (ICFs) for phase I oncology trials …
Levels of knowledge and perceived understanding among participants in cancer clinical trials–factors related to the informed consent procedure
M Bergenmar, H Johansson, N Wilking - Clinical trials, 2011 - journals.sagepub.com
Background An informed consent from patients participating in cancer clinical trials is
mandatory according to international and national guidelines and laws. Insufficient …
mandatory according to international and national guidelines and laws. Insufficient …