The Revised Common Rule requires all clinical trials to post an unsigned consent form on a publicly available website. The Revised Common Rule is in effect for studies approved on or after January 21, ...

Prospective assignment of participants to one or more interventions (which may include placebo or other control); Evaluation of the effects of the interventions on biomedical or behavioral ...

We have answered all your questions about the clinical trial. You understand the possible benefits and risks of participating in a clinical trial. You have signed and submitted your informed consent ...

When recruiting for a clinical trial: if you’re involved with designing and conducting clinical trials, you’d be wise to seek participants’ consent for these things upfront (as well as ...

This article describes how the South supra-region of the NIHR Clinical Research ... to an evaluation form. Once they have completed the evaluation, they can download their course certificate. This ...

To gain a more detailed understanding, unstructured free-text responses describing clinical trial discussions were also analyzed through language modeling. Overall, 57% of patients (540/955) preferred ...