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MEASUREMENTS: Hemoglobin A 1c) level and systolic blood pressure, measured by blinded research personnel at baseline, study midpoint (median, 6.8 months), and study completion (median follow-up, 12.8 months).
Therefore, blinded research nurses assess the outcomes.
Therefore, blinded research nurses assessed outcomes to minimise detection bias.
An independent and blinded research nurse administered the PASI during several patient visits to the outpatient clinic.
The majority of the outcomes were measured using questionnaires or were assessed by an independent, blinded research nurse.
The blinded research nurse will identify these complications for each patient in the trial and HES data will be used as a secondary recording method.
To ensure accurate collection the 30-day HPA patient self reported questionnaire was recorded in all patients collected by telephone, by a blinded research nurse.
A blinded research nurse followed up more than 85% by telephone, including 613 at 12 weeks and 600 at 24 weeks postpartum.
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He has no explanation for this phenomenon, but appropriately encourages further double-blinded research.
These interviews will be performed by non-blinded research assistants.
Pre- and post-intervention measures are being gathered by questionnaires administered face-to-face by a treatment-blinded research associate.
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