| Literature DB >> 27598694 |
Anando Sen1, Patrick B Ryan1,2, Andrew Goldstein1,3, Shreya Chakrabarti1, Shuang Wang4, Eileen Koski5, Chunhua Weng1.
Abstract
Randomized controlled trials can benefit from proactive assessment of how well their participant selection strategies during the design of eligibility criteria can influence the study generalizability. In this paper, we present a quantitative metric called generalizability index for study traits 2.0 (GIST 2.0) to assess the a priori generalizability (based on population representativeness) of a clinical trial by accounting for the dependencies among multiple eligibility criteria. The metric was evaluated on 16 sepsis trials identified from ClinicalTrials.gov, with their adverse event reports extracted from the trial results sections. The correlation between GIST scores and adverse events was analyzed. We found that the GIST 2.0 score was significantly correlated with total adverse events and serious adverse events (weighted correlation coefficients of 0.825 and 0.709, respectively, with P < 0.01). This study exemplifies the promising use of Big Data in electronic health records and ClinicalTrials.gov for optimizing eligibility criteria design for clinical studies.Entities:
Keywords: adverse events; clinical trials; eligibility criteria; generalizability; population representativeness; trait dependencies
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Year: 2016 PMID: 27598694 PMCID: PMC5266625 DOI: 10.1111/nyas.13195
Source DB: PubMed Journal: Ann N Y Acad Sci ISSN: 0077-8923 Impact factor: 5.691