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The Data collector will be given a comprehensive knowledge of the entire study process.
The data collector will be blinded to the arm of the trial to which the participant was randomized.
The project data collector will be responsible for the administration of the surveys, and informed consent will be obtained from all participants.
If the selected address is found to be from an excluded category, the data collector will be supplied with a new randomly selected address.
A data collector will be hired in each community cluster that will be responsible to identify, in collaboration with CMWs, TBAs and LHWs, all the women who have recently delivered in the area.
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Data collectors will be blind to the treatment group assignment.
Data collectors will be selected among the health facility staff.
In cases where discrepancies exceed 20%, data collectors will be retrained.
Data collectors will be independent from LHWs and will be selected based on their high level of performance in previous work at the same study site.
During training, data collectors will be required to conduct an observed interaction with a mother and newborn in the community to ensure standardization and quality data collection.
For each session, the data collectors will be dressed in plain clothes and use a separate room free from distractions for the focus groups.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com