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Published on: January 8, 2020
A reanalysis of cluster randomized trials showed interrupted time-series studies were valuable in health system
Atle Fretheim1, Fang Zhang2, Dennis Ross-Degnan2
1Department of Population Medicine, Harvard Medical School and Harvard Pilgrim Health Care Institute, 133 Brookline Avenue, Boston, MA 02215, USA; Global Health Unit, Norwegian Knowledge Centre for the Health Services, PO Box 7004, St. Olavs pl, 0130 Oslo, Norway; Department of Community Medicine, Institute of Health and Society, University of Oslo, PO Box 1130 Blindern, 0318 Oslo, Norway.
Objectives:
There is often substantial uncertainty about the impacts of health system and policy interventions. Despite that, randomized controlled trials (RCTs) are uncommon in this field, partly because experiments can be difficult to carry out. An alternative method for impact evaluation is the interrupted time-series (ITS) design. Little is known, however, about how results from the two methods compare. Our aim was to explore whether ITS studies yield results that differ from those of randomized trials.
Study Design And Setting:
We conducted single-arm ITS analyses (segmented regression) based on data from the intervention arm of cluster randomized trials (C-RCTs), that is, discarding control arm data. Secondarily, we included the control group data in the analyses, by subtracting control group data points from intervention group data points, thereby constructing a time series representing the difference between the intervention and control groups. We compared the results from the single-arm and controlled ITS analyses with results based on conventional aggregated analyses of trial data.
Results:
The findings were largely concordant, yielding effect estimates with overlapping 95% confidence intervals (CI) across different analytical methods. However, our analyses revealed the importance of a concurrent control group and of taking baseline and follow-up trends into account in the analysis of C-RCTs.
Conclusion:
The ITS design is valuable for evaluation of health systems interventions, both when RCTs are not feasible and in the analysis and interpretation of data from C-RCTs.
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