Rather, it is participation in communication.
Was participation in them recorded?
Blood pressure, height, and weight data were collected before participation in any trips.
We enrolled 4 comparison families matched to the case family that declined participation; these data were included in the cross-sectional analysis but not in the case-comparison analysis.
The patient or his/her legal guardians signed informed consent for participation before any data were included in the study.
Qualitative data were gathered through interviews, participation in meetings, action research, and review of company documents.
Although platelet count data were not required for participation in the focus groups, clinicians at each site considered the subjects to have active disease, usually an indication that platelet levels have dropped below 120 × 10L and the subject requires treatment and/or more frequent monitoring.
Data were collected in the school setting after an agreement of participation of all the schools.
In terms of participation, we found that our participation data were comparable to prior research using physics RBAs across several dimensions, including genders and grades.
The 2012 data were collected through the Swiss participation in the QUALICOPC study.
