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Data collection for Study 1 was undertaken by the epidemiological research group in the selected classrooms.
MH is involved in carrying out the study and data collection for study 1.
However, after successful data collection for study purposes we did not manage to integrate the use of the PRO results into individual patient treatment.
Three research assistants administered the HKECDS (Trial Version 2) in Study 2. Two of them had been involved in the data collection for Study 1.
If informed consent could not be obtained, the Finnish National Institute of Health and Welfare approved the data collection for study purposes from deceased patients.
Data collection for Study 116 did not begin until individual participation in Trial 204 was over or between/after participation in Trial 208, if the patient also participated in the extension trial.
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We applied this time lag to estimate the year of data collection for studies missing this value.
The data collection for this study was collected from a Multivariable Calculus class at UTM during semester II 2009-2010.
HC and MJ initiated and managed data collection for the study, clinical data were collected by HC and NB.
All members of this EUROHIP study group advised and/or contributed to the design and data collection for this study.
Data collection for this study was completed using a quantitative survey.
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