Sentence examples for trials sharing from inspiring English sources

Exact(5)

The present study used a mixed fMRI design to investigate whether adoption of different retrieval orientations – as indexed by differences in the activity elicited by retrieval cues corresponding to unstudied items – is associated with differences in the state-related activity sustained across a block of test trials sharing a common retrieval goal.

The Internet is a powerful tool for broadcasting the availability of clinical trials, sharing news about research and treatment breakthroughs, and providing both patient and caregiver support.

Pairwise meta-analyses combine the results of homogeneous studies conducted on the same topic, whereas network meta-analyses evaluate simultaneously both direct and indirect comparisons across trials sharing one or more common comparators [ 21– 23].

A 2 × 2 ANOVA of reaction times with factors rhyming (rhyming, nonrhyming) and spelling (congruent, incongruent) did indeed reveal an interaction in the predicted direction, with relatively faster responses for rhyme trials sharing spellings and relatively slower responses for nonrhyme trials with similar spellings, but this effect fell short of significance (F1,11 = 2.92, P = 0.12).

44 Academic institutions and promotions committees need to begin crediting investigators not just for publishing articles in high-impact journals, but also for creating data by designing and conducting clinical trials, sharing data with other investigators and enabling them to address important questions.

Similar(55)

Although all randomized controlled clinical trials share basic design characteristics, to assess the outcome of a particular trial one must carefully evaluate specific details of its design and analysis that might bias the study and influence its results.

We also found the binding modes with lowest energy generated from other 5 trials shared some common features with the native binding mode in the last trial.

The two trials share the following scientific objectives, which will contribute evidence towards the identified evidence gaps.

Both multicenter, randomized, double-blind, placebo-controlled phase III trials shared similar objectives and methods, and elicited comparable efficacy and safety data.

Participants in these trials shared data while formally enrolled under protocols in which they were meant to be blinded and unaware of their ALSFRS-R score.

57 In spite of their heterogeneous nature, the 21 selected trials share a medicotechnological context in which an a priori enhanced placebo response could be expected.

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