The technology’s potential to transform trials will need to be balanced with the challenge of instilling trust in participants.

Background Alternatives to prospective informed consent enable the conduct of paediatric emergency and critical care trials. Research without prior consent ... A range of sites were included to ensure ...

Objective A mixed-methods study exploring the UK general public's views towards consent for ... biosamples for research use. The majority (65%) wanted to do so face-to-face with a health professional; ...

This study provides a broad assessment of the complexity level of clinical research Patient Information Leaflets/Informed Consent Forms (PILs/ICFs), including ... To characterise the sample set, ...

We must receive your signed consent form at the time you submit your files ... wishes to allow the free reproduction of published material for educational and/or research purposes. Therefore, the ...

These consent forms were presented to patients by their physician ... Then, the use of verbal consent will be evaluated in three sample cases–COVID-19 research, rare disease research, and clinical ...

The European Union’s General Data Protection Regulation requires every organization that collects sensitive personal data from those residing in the EU to ask for clear and specific consent ...

we want them to sign a consent form or something like that. That’s an idea we had. We only interviewed a modest sample of students from Perth. But our study feeds into other research suggesting ...

Informed consent ... a blood sample drawn and roll up your sleeve, your consent is implied. Except under specific circumstances, informed consent—whether written or implied—is required for any ...

The trial used simplified opt-out consent with concise parent information and no consent form. Objective To explore the views ... data saturation was reached within a demographically varied sample.21 ...