Citation: Foxton J et al (2025) Informed consent training for clinical research trials: online delivery ... the delegates are automatically emailed a link to an evaluation form. Once they have ...

Study results suggest that “telemedicine represents a unique opportunity to reduce time and travel burdens for patients with cancer considering clinical trials,” according to researchers.

consent must be re-requested from the participant, who must re-read lengthy forms containing complex terminology, which can affect retention. It isn’t abnormal for clinical trials to require ...

Data in and of itself can be interesting, but the true value of data lies in how you use it and the insights that come from ...

The primary value of placebo controls in clinical trials is the minimization of bias.

The Revised Common Rule includes a requirement specific to clinical trials to post an informed consent form used to enroll participants on a publicly available website. A study involves the ...

You understand the possible benefits and risks of participating in a clinical trial. You have signed and submitted your informed consent form. Before you decide to take part in a clinical trial, ...

The survey assessed patients' preferences for telemedicine versus in-person visits for the IC process and their comfort with discussing clinical trials virtually. The primary outcome was the ...

Multiple vaccine-related petitions that have been filed before courts reflect growing concerns about how vaccines are ...

The EDC system enables seamless data collection and real-time monitoring across all participating sites. The clinical trial is designed to evaluate the safety, tolerability and efficacy of Clearmind’s ...