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 ...

Informed consent is one of the primary requirements of research involving human participants ... provided the conditions described on the waiver form are fulfilled.

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, ...

Contemporary Clinical Trials 31: 394-404 (2010) 2. Rubinstein, YR, et al. Informed consent process for patient participation in rare disease registries linked to biorepositories. Contemporary ...

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 ...

Many types of clinical trials rely upon voluntary participation. Most clinical studies, but not all, test new drugs. Informed consent is the process of learning the key facts about 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 ...