Sentence examples for describe consent from inspiring English sources

This paper will describe consent rates for a sample of socially disadvantaged smokers who were approached to participate in an Australian trial Call it Quits (CiQ)—to increase cessation among a socially disadvantaged group of smokers.

Human FLS were isolated from synovial tissues from four different RA patients at the time of knee joint arthroscopic synovectomy as described previously after informed consent was obtained from patients [35].

Describing "Consent" as an exploration of "desire, vulnerability, passion and shame," Rhodes ("Rites of Privacy") based much of the plot on his own coming out experience.

In the introduction to a 2008 report by the Alabama Policy Institute, a conservative think tank, Sessions described consent decrees as "dangerous" "exercises of raw power" that "constitute an end run around the democratic process".

In the introduction he wrote to a 2008 report from conservative think tank the Alabama Policy Institute, Sessions described consent decrees as "dangerous" and creating a "run around the democratic process".

As previously described consent was obtained from parents or guardians and verbal consent was obtained from children [ 13, 14].

The Victorian State Trauma Registry protocol, including the described consent process, has been approved by the Human Research Ethics Committee at each participating hospital and the Monash University Human Research Ethics Committee.

Authors may, therefore, have considered a statement of "agreement" as adequate when describing consent practices from health professionals or other participants at the cluster level but used more conventional descriptors when reporting consent practices at the level of the individual patient.

To demonstrate the differences in these approaches to informed consent, we describe the consent processes for two MPS studies.

Walport described the consent for consent situation as ridiculous.

To assess participants' knowledge of key aspects about the clinical trials in which they are enrolled, describe the consent process, and assess the importance that investigators give to various aspects of trial information when verbally informing candidates.