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Data collection for the control group was completed first, followed by data collection for the other 2 groups.
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Data collection for the cases and controls included important social and demographic information, and examined general health, lifestyle, and medication use.
Participating schools (n=178) were randomised to receive the 'Hands up for Max!' educational package in October 2009 (intervention schools, n=88) or to receive the resource after follow-up data collection for the main trial was completed (control schools, n=90).
The interviews for HUAS and for HUAS-Lite rounds and the data collection for the case/control study were conducted by locally employed and trained health workers in each country.
Data collection for the study is complete.
The BGS contains a nested case control study for analyses, where data collection for the full cohort is not feasible.
BP readings that were recorded as 'free text', rather than on the practice computer electronic template, may not have been noted during the data collection for control patients.
Clinical data were grouped into 1-hour blocks for 24 hours ending at the event for case patients or at the end of 12 hours of data collection for control patients.
Data collection in all three states occur at baseline (prior to the first lesson of the HT or the control intervention), at post (after completion of the eighth lesson, after 3 months for controls), and at 6 months after completion of the 2nd data collection for both the intervention and control groups.
The three data collection points were: Baseline: four weeks before the intervention Four weeks after the intervention workshops (for the intervention group) were completed Six months after the first post-intervention data collection was completed Data collection for both the intervention and control arms took place during similar periods at every time point.
This has resulted in a unified system of data collection for research and quality control.
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