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To attend emergency department as a result of physical complications. Our participants were more informed about the ongoing haze, associated possible physical dangers as well as the steps taken by the government. These factors might have influenced their responses. Third, the list of physical symptoms was derived from general medical knowledge and it was not designed to detect specific physical sy
1
Omen with bothersome symptoms first increased and then decreased. Conclusions: There was a notable variability in the development of disturbing vasomotor symptoms over time in a selected group of women aged 50?9. Population-based follow-up studies of untreated women would be useful to estimate the symptom burden. Keywords: Menopausal symptoms, Duration, Follow-up, EstoniaBackground A number of stu
1
Omen with bothersome symptoms first increased and then decreased. Conclusions: There was a notable variability in the development of disturbing vasomotor symptoms over time in a selected group of women aged 50?9. Population-based follow-up studies of untreated women would be useful to estimate the symptom burden. Keywords: Menopausal symptoms, Duration, Follow-up, EstoniaBackground A number of stu
1
Omen with bothersome symptoms first increased and then decreased. Conclusions: There was a notable variability in the development of disturbing vasomotor symptoms over time in a selected group of women aged 50?9. Population-based follow-up studies of untreated women would be useful to estimate the symptom burden. Keywords: Menopausal symptoms, Duration, Follow-up, EstoniaBackground A number of stu
1
To attend emergency department as a result of physical complications. Our participants were more informed about the ongoing haze, associated possible physical dangers as well as the steps taken by the government. These factors might have influenced their responses. Third, the list of physical symptoms was derived from general medical knowledge and it was not designed to detect specific physical sy
1
Not included in the present analysis. The women in the blind arms received their drug bottles with coded labels (otherwise identical bottles). Women in the non-blind HT arm had their drug bottles marked with HT. Only data on women in blind placebo group and nontreatment group aged 50?9 at recruitment (n = 486) are used in this study. Throughout the trial, about 90 ofwomen in the non-treatment gro
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R correlation from primary care research to inform study design and analysis. J Clin Epidemiol 2004, 57 (8):785?94. 52. Schulz KF, et al: CONSORT 2010 Statement: updated guidelines for reporting parallel group randomised trials. BMC Med 2010, 63(8):834?40.doi:10.1186/1471-2393-12-155 Cite this article as: Kempler et al.: Sleep education during pregnancy for new mothers. BMC Pregnancy and Childbirt
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E therapy to either placebo or nothing (the control groups) [21]. Women were recruited in Estonia from 1999?001, and followed by annually mailed questionnaires in 2000?004. Detailed descriptions of the recruitment, inclusion and exclusion criteria, trial treatment, adherence, follow-up and trial outcomes as well as the content of information leaflets and trial questionnaires have been published el

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