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The initial data collection for this study was completed between 2006 2007.
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The initial data collection was undertaken for 7 days from midnight on 1 March until midnight on 8 March 2010.
The pre-publication history for this paper can be accessed here: http://www.biomedcentral.com/1471-2296/13/122/prepub The authors would like to acknowledge the contributions of Tiffany Kwok, who was involved in the initial data collection and interviews for this study.
Mandatory variables included on the initial data collection form and used for this study were: age, gender, race (black non-Hispanic, white non-Hispanic), type of practice, size of the largest polyp detected at colonoscopy, number of polyps (single versus ≥ 2), any family history of colorectal cancer (positive, negative) and polyp location defined as proximal or distal to the splenic flexure.
"The initial data collection sheet did not ask for data regarding loss of consciousness," that paper said.
These results were presented to the district information officers responsible for the data submissions to the DHIS and to many of the clinic managers responsible for the initial data collection.
Following informed consent, separate home visits were scheduled for the initial data collection.
Once eligibility is established, families are contacted for the initial data collection home visit where written informed consent is obtained.
The coordinator was present with the patients for the initial data collection, to answer their questions and to verify integrity of the data.
NH was also responsible for the initial data collection at the GNC (Zambia) and NMC and coordinated the writing of this paper.
For details on the initial data collection, see the work by Tick et al. [ 19].
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