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Protein sources were assessed by two unannounced 24-hour recalls at each of three study visits.
Methods: Fifteen normal weight women (18 45 year) were randomized in a crossover design to complete three study visits.
Adult participants (n=809) who completed the 18-month PREMIER lifestyle intervention trial and had at least one diet recall at each of three study visits were included.
Information about type and dose of concomitant medications was collected at each of the three study visits (screening, baseline and end of treatment).
Differences in plasma HIV RNA and CD4+ T cell counts between groups were explored longitudinally across three study visits and cross-sectionally at the last study visit.
The degree of HSV-2 clinical activity among symptomatic women was then graded from: a) mild symptomatic (only self report positive but no lesions at any study visit), b) mild to moderate (lesions at only one of the study visits), c) moderate (lesions at two visits), and d) severe symptomatic (lesions at all three study visits).
Similar(21)
Between July 2010, and August 2012, 144 randomly selected participants were screened for VOICE-C eligibility during or following their VOICE month three study visit.
Among women who tested positive for laboratory-confirmed BV/TV at any of the three study visit, only the first visit at which the participant was positive was included in the BV/TV dataset.
Participants attended for two study visits.
Each study subject had two study visits.
Each patient underwent four study visits.
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