Sentence examples for features of trial from inspiring English sources

Exact(4)

Overall, features of trial participation meant that participants reported that attending the commercial programme during the trial was different from if they had been more usual attendees.

The provision of information about key features of trial quality (and/or about quality assessment) was thought desirable for a centralised resource.

Seven features of trial design and conduct may distinguish a pragmatic RCT from an efficacy or more theoretically driven RCT [ 61].

Before starting the review we hypothesised that several features of trial design might affect the outcome of cholesterol lowering trials of statins.

Similar(55)

A cerebellar circuit model that reproduces the features of trial-over-trial depression of simple-spike firing rate and trial-over-trial learning in eye velocity.

Other key features of trials showing improvement is the selection of patients at high risk of adverse outcomes.

Several articles described seven pivotal features of trials that would need to be considered when making decisions about the appropriateness of patient reported outcomes in clinical trials.

While trial discontinuation for apparent benefit has been investigated previously [ 24, 25], little is known about the epidemiology and features of trials discontinued for other reasons, in particular for insufficient recruitment.

The other features of trials such as follow-up visits and extra time spent discussing the child's condition are often perceived by parents as direct benefits of participation (e.g. [ 84- 87]).

As indicated in the methods section, we explored two approaches that might help people evaluate information about trials and assess their quality: (a) a quality or "star" rating scheme in which key features of trials were allocated one- to three- star ratings; and (b) a guide to help people appraise trials for themselves.

RCTs are, of course, rarely straightforward to design and implement, 65 68 and features of trials that may be critical in the context of medicinal products, such as randomising, and single or double-blinding, may either be impractical or irrelevant when intervening in health service delivery, while others, such as blinding of assessors, will remain essential.

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