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The following considerations were addressed: participation was voluntary; refusal to participate did not affect care received; participants were fully informed of the nature of the study and of their rights and obligations; signed, informed consent was obtained from all participants; and participants were assured that their information would be kept confidential.
In the letters they received, participants in the Women's Health Initiative were urged to stay in the study.
From the replies received, participants of this study fall into the third group.
However, when we received participants' plasma specimens, the viral subtypes were unknown and the clinical trial's time constraints precluded sequencing from additional unlinked participants.
If no response is received, participants are contacted by phone.
Fourthly, once written consent was received, participants were tested for inclusion and exclusion criteria.
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Recruitment strategies were rolled out when practices were ready to receive participants for the study.
Eligible women receive participant information.
A total of 7611 participants received treatment; 3783 participants received TIV, and 3828 received placebo.
Furthermore, it was well received by participants.
Participants received $20 for participation.
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