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At each site, baseline data are collected in person and via electronic record at enrollment into the program.
Randomization was stratified by site, baseline HbA1c control (≥9.0 vs. <9.0%), and baseline systolic BP (≥150 mmHg vs. <150 mmHg).
Randomisation was stratified by investigational site, baseline weight (≤/>100 kg), and baseline methotrexate (MTX) usage (yes/no).
Models also included our stratification variables of site, baseline BP (systolic BP ≥150 mmHg vs. systolic BP < 150 mmHg) and baseline HbA1c (HbA1c ≥9.0 vs. <9.0%).
These findings remained significant after adjusting for age, sex, race, clinic site, baseline BMI, weight change intention, and actual weight changes over time.
These regression models will include gender, investigative site, baseline A1C, age group, diabetes duration and body mass index as predictor variables.
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Many cross-site baseline differences disappeared when we took referral source into account, but not all.
When multivariable adjustments were performed to account for site-, baseline morbidity-, and other clinical- and socioeconomic differences (Table 3), the significant association of K-10 score [OR = 1.082 1.0333, 1.137); p = 0.0012] and health literacy [OR = 0.798 (0.696, 0.906); p = 0.0008] with non-adherence persisted.
Data presented here are from each sites' baseline survey.
At bretylium-treated sites baseline CVC values did not differ significantly between age groups.
Table 2 provides data on enrolments at rural and urban sites, baseline HIV prevalence and HIV incidence in pregnant women.
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