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The effect of the Fortaleça sua Saúde program on the primary variables will be tested in accordance with the intention-to-treat principle and in a completers-only framework using Mplus [ 55].
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The primary variable will be analysed using a two-way analysis of covariance.
Primary outcome variables will be treated as statistically independent.
Only primary outcome variables will be used in the 27 months follow-up assessment.
Primary outcome variables will be self-reported disability and pain intensity.
The primary exposure variables will be dietary consumption of n-3 and n-6 polyunsaturated fatty acids.
The effectiveness of our home-based educational intervention for the primary outcome variables will be analyzed with mixed modeling, i.e. multilevel regression modeling.
Primary Exposure/Demographic Variables will be characterized as baseline DDLS score, age, ethnicity, gender, type of glaucoma, and number of medical comorbidities.
Primary Outcome Variables will be divided into three groups: 1) QoL (NEI-VFQ-25 and MGSS) 2) performance-based measures of visual function (CAARV) and 3) Clinical measures of vision (better and worse eye VF mean defect, better and worse eye VA, and binocular SPARCS contrast sensitivity).
Descriptive statistics (mean, median, number of observations, standard deviation, standard error, 95% confidence intervals - minimum and maximum) of all primary and other variables will be tabulated.
Bowel, cervical and breast screening history as well as primary CRC pathology variables will be retrieved for all cases and controls.
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