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Among the 123 patients who took part in an end of study interview and who did not take psychotropic drugs at inclusion, 13 patients (10.6%) had used psychotropic medications during the follow-up period.
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Additional data were collected during the initial visit, subsequent visits, and end-of-study interview.
Radio announcements were also used to request women to provide the end-of-study interview.
If the women did not return for the end-of-study interview the research assistant contacted them either by phone or directly.
All 103 completed the enrollment visit, and 102 (99.0%) caregivers completed the end-of-study telephone interview 15 to 18 days after enrollment; 20 (19.4%) caregivers completed all 14 days of the GRCD (overnight and daytime symptom diaries); 62 (60.2%) completed 10 or more days, and 89 (86.4%) completed the diaries for 7 days or more.
Outcomes will be measured from baseline and end of study exit interview data, FGDs and interviews.
At the end of the study, interviews with the GPs will be conducted to assess the perceived effort for the practices.
At the end of the study, interviewers, Prismant, and institutions discussed about how the interviews had been conducted.
Follow‐up time was calculated from interview date/examination date until date of death or end of study (31 December , 2011, whichever came first.
EOS end of study.
At the end of each interview, interviewers reviewed their notes.
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