2011
DOI: 10.1186/1472-6963-11-331
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A randomized trial of an intervention to improve use and adherence to effective coronary heart disease prevention strategies

Abstract: BackgroundEfficacious strategies for the primary prevention of coronary heart disease (CHD) are underused, and, when used, have low adherence. Existing efforts to improve use and adherence to these efficacious strategies have been so intensive that they are impractical for clinical practice.MethodsWe conducted a randomized trial of a CHD prevention intervention (including a computerized decision aid and automated tailored adherence messages) at one university general internal medicine practice. After obtaining… Show more

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Cited by 67 publications
(59 citation statements)
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“…Additionally, the timeframe of a majority of studies was between 6 and 12 months, and most studies were published within the past decade. RCTs were blinded with specific mention of study personnel blinded to allocation and grouping during the study and to data analysis, with the exception of three studies 1921 .…”
Section: Resultsmentioning
confidence: 99%
“…Additionally, the timeframe of a majority of studies was between 6 and 12 months, and most studies were published within the past decade. RCTs were blinded with specific mention of study personnel blinded to allocation and grouping during the study and to data analysis, with the exception of three studies 1921 .…”
Section: Resultsmentioning
confidence: 99%
“…Based on a previous study [12], we estimated that the within-practice intraclass correlation for change in systolic BP was zero and standard deviation was 16 mmHg. We assumed that the baseline difference in systolic blood pressure between African Americans and Whites would be approximately 5 mmHg.…”
Section: Methodsmentioning
confidence: 99%
“…25 Several studies completed because this review have also demonstrated significant improvements in risk factor levels, and increased the use of preventive medication. 15,26,27 One difference between this study and most previous trials is that we used a pragmatic design with a waiver of informed consent that included all eligible patients receiving care at participating sites. Therefore, our findings may be more indicative of how this type of intervention performs in a general population rather than one limited to volunteer participants.…”
mentioning
confidence: 99%