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Optimized Probability Sampling of Study Sites to Improve Generalizability in a Multisite Intervention Trial
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Dec 15 2009
Source: Prev Chronic Dis. 7(1).
[PDF-408.35 KB]
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Alternative Title:Prev Chronic Dis
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Description:Introduction
Studies of type 2 translation, the adaption of evidence-based interventions to real-world settings, should include representative study sites and staff to improve external validity. Sites for such studies are, however, often selected by convenience sampling, which limits generalizability. We used an optimized probability sampling protocol to select an unbiased, representative sample of study sites to prepare for a randomized trial of a weight loss intervention.
Methods
We invited North Carolina health departments within 200 miles of the research center to participate (N = 81). Of the 43 health departments that were eligible, 30 were interested in participating. To select a representative and feasible sample of 6 health departments that met inclusion criteria, we generated all combinations of 6 from the 30 health departments that were eligible and interested. From the subset of combinations that met inclusion criteria, we selected 1 at random.
Results
Of 593,775 possible combinations of 6 counties, 15,177 (3%) met inclusion criteria. Sites in the selected subset were similar to all eligible sites in terms of health department characteristics and county demographics.
Conclusion
Optimized probability sampling improved generalizability by ensuring an unbiased and representative sample of study sites.
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Pubmed ID:20040225
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Pubmed Central ID:PMC2811505
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