2014
DOI: 10.1186/s13012-014-0096-x
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How pragmatic is it? Lessons learned using PRECIS and RE-AIM for determining pragmatic characteristics of research

Abstract: BackgroundThe need for high-quality evidence that is applicable in real-world, routine settings continues to increase. Pragmatic trials are designed to evaluate the effectiveness of interventions in real-world settings, whereas explanatory trials aim to test whether an intervention works under optimal situations. There is a continuum between explanatory and pragmatic trials. Most trials have aspects of both, making it challenging to label and categorize a trial and to evaluate its potential for translation int… Show more

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Cited by 97 publications
(99 citation statements)
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“…During the trial, some CHAs made modifications to the study protocol, such as referring participants to the free clinic even if they had health insurance and conducting educational sessions with individuals rather than with small groups. We did not interfere with these modifications and captured them in our assessments, as recommended for implementation research [30,31].…”
Section: Methodsmentioning
confidence: 99%
“…During the trial, some CHAs made modifications to the study protocol, such as referring participants to the free clinic even if they had health insurance and conducting educational sessions with individuals rather than with small groups. We did not interfere with these modifications and captured them in our assessments, as recommended for implementation research [30,31].…”
Section: Methodsmentioning
confidence: 99%
“…Determinations were made for each criterion using a simple binary system to indicate whether the study met pragmatic criteria (yes = 1) or not (no = 0), where a maximum score of 11 could be assigned per study (Supplementary Table 2). After being trained to code [15], two independent raters (KL and KW) evaluated each study. Interrater agreement of coding for a random sample of studies (N=30) was determined to be 78%.…”
Section: Methodsmentioning
confidence: 99%
“…See Fig. 1 for the overview of the study using the expanded CONSORT model linking the RE-AIM framework, data sources, and measures used [21,29]. The University of Iowa Institutional Review Board approved all aspects of the study.…”
Section: Methodsmentioning
confidence: 99%
“…The reason for this longitudinal sample was to understand the effect of the intervention under real-world conditions, so no attempt at randomization was made [29]. Rather, recruiting a sample of patients and following them during the implementation period was meant to provide additional estimates of reach, and access to a comparison group exposed to similar clinical conditions (i.e., practice context and medical management), but not necessarily to the intervention over the 9-month study period.…”
Section: Implementation Resourcesmentioning
confidence: 99%