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■ Abbreviation / Long Form : ICFs / informed consent forms

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Abbreviation:   ICFs  (>> Co-occurring Abbreviation)
Long Form:   informed consent forms
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No. Year Title Co-occurring Abbreviation
2020 Does content of informed consent forms make surgeons vulnerable to lawsuits? ---
2020 Evaluation of length and complexity of written consent forms in English and Hebrew for participation in clinical trials authorized in one medical institution in Israel: A descriptive study. ---
2019 Assessing readability and comprehension of informed consent materials for medical device research: A survey of informed consents from FDA's Center for Devices and Radiological Health. CDRH, IC, IDE
2018 A comparison of the quality of informed consent for phase I oncology trials over a 30-year period. ---
2018 Patient consent to publication and data sharing in industry and NIH-funded clinical trials. BioLINCC
2018 Trends of Informed Consent forms for industry-sponsored clinical trials in rheumatology over a 17-year period: Readability, and assessment of patients' health literacy and perceptions. HL
2018 What information and the extent of information research participants need in informed consent forms: a multi-country survey. ---
2017 Evidence-Based Strategies for Shortening Informed Consent Forms in Clinical Research. HPTN
2017 Informed consent in oncology clinical trials: A Brown University Oncology Research Group prospective cross-sectional pilot study. ---
10  2017 Informed Consent to Study Purpose in Randomized Clinical Trials of Antibiotics, 1991 Through 2011. SAPs
11  2017 Social and Communicative Functions of Informed Consent Forms in East Asia and Beyond. ---
12  2016 Comparison of good clinical practice compliance and readability ease of the informed consents between observational and interventional clinical studies in the Emirates. GCP
13  2016 Disclosure of amyloid status is not a barrier to recruitment in preclinical Alzheimer's disease clinical trials. AD
14  2016 Readability and Content Assessment of Informed Consent Forms for Phase II-IV Clinical Trials in China. ---
15  2016 Readability of informed consent forms in clinical trials conducted in a skin research center. CRTSDL
16  2016 SIDCER informed consent form: principles and a developmental guideline. SIDCER
17  2015 [Quality and legibility of written informed consent form in pharmacogenetic research]. ---
18  2014 Informed consent for phase I oncology trials: form, substance and signature. ---
19  2013 Giving consent without getting informed: a cross-cultural issue in research ethics. ---
20  2012 Easy-to-read informed consent forms for hematopoietic cell transplantation clinical trials. BMT CTN, HCT, IRB, US
21  2009 Access to medications and medical care after participation in HIV clinical trials: a systematic review of trial protocols and informed consent documents. ACTG, ARV, FDA
22  2009 Critical evaluation of informed consent forms for adult and minor aged whole blood donation used by United States blood centers. GIFs, PCFs
23  1996 Informed consent for medical research: common discrepancies and readability. IRBs