As such, we analyzed the data by six study centers in five countries.
Participants received their breakfast (test meal) under supervision by one of the two study centers over four consecutive mornings.
For the comparison of CSP-specific CD4 T cell responses induced by RTS,S/AS01E and RTS,S/AS02D, data from the two study centers for the 0,1- and 0,1,7-month schedules were pooled.
As a consequence of site audits conducted by the study sponsor GlaxoSmithKline, concerns about the quality of data supplied were identified for two study centers.
This study examined the factor structure of the BAVQ-R by combining datasets from five study centers, comprising 450 participants (belief constructs) and 269 participants (response styles), and using confirmatory and exploratory factor analysis.
Populations from eight study centers were selected by national stakeholders.
The integrated results from the four study centers were validated by the (co- moderators (MB, NL, JMFA, EK) of all partico- moderatorsries.
Second, the participants who were suspected of having dementia on the basis of their neuropsychological performance (in particular the Mini Mental Status Examination, the Benton Visual Retention Test, and the Isaac's Set Test administered uniformly in all three study centers at each follow-up [ 16]) were examined by a neurologist in the three study centers (16).
Eight study centers enrolled patients; 2 centers did not participate due to organizational reasons.
The data for this study was collected in five study centers in four countries.
