postpartum depression. Mild mental and behavioural disorders associated with the puerperium, not elsewhere classified
Conditions
Interventions
Intervention 1: Case group receive {2 tablets B6 (40mg
oral) daily
from week 28 till end pregnancy
after delivery1 tablet B6 (40mg
oral) daily for one month}. Every two weeks, Researcher phone calls to ensure, they were reminded of pills on phone and mentioned the subjects’ use of pill. Edinburgh postpartum depression questionnai
daily from week 28 till end pregnancy, after delivery receiving placebo 1 tablet oral
daily for a month} . The Placebo tablet has 6.2 mm in diameter and 100 mg weight and made from corn starch. The placebo tablet is Simulated of vitamin tablet B6 Amin pharmaceutical factory. Every two
Placebo
Case group receive {2 tablets B6 (40mg
Control group receive { placebo 2 tablets oral
Sponsors
Isfahan Research Department of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: Inclusion criteria: The criterion for entering this study was at least one risk factor of postpartum depression; physical health of pregnant mother; lack of current depression. Exclusion criteria: prenatal depression at third trimester; unwillingness to continue the study at any time
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postpartum depression. Timepoint: The depression was evaluated baseline before intervention /and 1.5 month after delivery. Method of measurement: Edinburgh standard questioner. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMaryam khodadad
Isfahan University of Medical Science
Outcome results
None listed