Background: Before participation in medical research an informed consent must be obtained. This study investigates whether the readability of patient information and consent documents (PICDs) corresponds to the average educational level of participants in rheumatological studies in the Netherlands, Denmark, and Norway. Methods: 24 PICDs from studies were collected and readability was assessed independently using the Gunning's Fog Index (FOG) and Simple Measure of Gobbledygook (SMOG) grading. Results: The mean score for the FOG and SMOG grades were 14.2 (9.0-19.0) and 14.2 (12-17) respectively. The mean FOG and SMOG grades were 12.7 and 13.3 in the Dutch studies, 15.0 and 14.9 in the Danish studies, and 14.6 and 14.3 in the Norwegian studies...
Transparency Matters: A Review of Readability in Clinical Trial Informed Consent FormsBackground: Cl...
The scope of this project is to gauge the clinical researchers’ obtained knowledge of the consent fo...
WOS:000456457100010Aim: The aim of the present study was to evaluate the readability levels of infor...
Background: Before participation in medical research an informed consent must be obtained. This stud...
BACKGROUND: Quantitative tools have been developed to evaluate the readability of written documents ...
Quantitative tools have been developed to evaluate the readability of written documents and have bee...
National audienceOBJECTIVE: We compared informed consent forms of subjects participating in biomedic...
Objectives The first aim of this study was to quantify the difficulty level of clinical research Pat...
The aims of this study were to measure the readability of Australian based informed consent document...
Objectives: Patients are often provided with medicine information sheets (MIS). However, up to 60% o...
Researchers typically attempt to fulfill disclosure and informed consent requirements by having part...
Background Informed consent in research is partly achieved through the use of information sheets. Th...
Background: The validity of the informed consent process rests in part on whether potential study pa...
To conduct research ethically, informed consent must be obtained from each subject or a representati...
Background High quality of informed consent form is essential for adequate information transfer betw...
Transparency Matters: A Review of Readability in Clinical Trial Informed Consent FormsBackground: Cl...
The scope of this project is to gauge the clinical researchers’ obtained knowledge of the consent fo...
WOS:000456457100010Aim: The aim of the present study was to evaluate the readability levels of infor...
Background: Before participation in medical research an informed consent must be obtained. This stud...
BACKGROUND: Quantitative tools have been developed to evaluate the readability of written documents ...
Quantitative tools have been developed to evaluate the readability of written documents and have bee...
National audienceOBJECTIVE: We compared informed consent forms of subjects participating in biomedic...
Objectives The first aim of this study was to quantify the difficulty level of clinical research Pat...
The aims of this study were to measure the readability of Australian based informed consent document...
Objectives: Patients are often provided with medicine information sheets (MIS). However, up to 60% o...
Researchers typically attempt to fulfill disclosure and informed consent requirements by having part...
Background Informed consent in research is partly achieved through the use of information sheets. Th...
Background: The validity of the informed consent process rests in part on whether potential study pa...
To conduct research ethically, informed consent must be obtained from each subject or a representati...
Background High quality of informed consent form is essential for adequate information transfer betw...
Transparency Matters: A Review of Readability in Clinical Trial Informed Consent FormsBackground: Cl...
The scope of this project is to gauge the clinical researchers’ obtained knowledge of the consent fo...
WOS:000456457100010Aim: The aim of the present study was to evaluate the readability levels of infor...