We developed a path model to test the effects of the media campaign on conditional intention to get screened (Fig. 2).
Taken together, these data suggest that both rat and mouse models should be used to screen the acute hepatotoxic effects of drugs and toxic compounds.
For such a task, our model can be used to screen the target and simulate the effects of the intentional intervention.
In order to validate the model we are proposing to screen antineoplastic effect of natural compounds, we selected caffeic acid, ursolic acid, and rosmarinic acid.
Methods: a Markov model was designed to compare the effects of a single screening for a cohort of men 60-65 years with the current no screening strategy.
11 This allowed us to model the effects of some women having early and late re-screening after being returned to routine screening.
Therefore researchers often rely on modeling techniques in order to estimate the effects of screening for colorectal cancer.
Further interpretation and modelling are needed to predict the effects of multiple (more than two) screening rounds.
The implementation, extension, and steady-state phases of the Dutch screening program were modeled in MISCAN (11, 12), designed to assess the effects of screening on a population.
Despite these limitations, the model truly reproduces the effects of diabetes screening and lifestyle interventions.
