Postpartum depression, Anxiety. Postpartum depression, Mild mental and behavioural disorders associated with the puerperium, not elsewhere classified
Conditions
Interventions
Intervention 1: The intervention group will receive Pardehan syrup at a dose of 10 cc (equivalent to one tablespoon), three times a day for 30 consecutive days. Intervention 2: The control group will
Sponsors
Boushehr University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 40 Years
Inclusion criteria
Inclusion criteria: 1.Mothers with mild to moderate postpartum depression. 2.Mothers aged between 18 and 40 years, who are 2 to 12 weeks postpartum. 3. 4. 5. 6. Mothers aged between 18 and 40 years, who are 2 to 12 weeks postpartum. No use of antidepressant medications to manage the condition. Birth of a healthy infant.Mothers must have at least basic literacy (reading and writing skills). Pregnancy must have been low-risk. Maternal body mass index (BMI) must be less than or equal to 40 kg/m².
Exclusion criteria
Exclusion criteria: Mother's unwillingness to continue participating in the study to receive syrup for 2 consecutive days Sensitivity to Pardihan syrup A history of previous depression with an unrelated cause A history of taking antidepressants Women who suffer from other mental illnesses or take related medications having Diabetes having Polycystic ovary syndrome Failure to complete the course of taking interventions
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Depression score. Timepoint: Filling out the questionnaire will be done at the beginning of the study (before the intervention) and 30 days after the start of the study. Method of measurement: Physical Health Questionnaire (PHQ). | — |
Secondary
| Measure | Time frame |
|---|---|
| Sleep quality. Timepoint: Filling out the questionnaire will be done at the beginning of the study (before the intervention) and 30 days after the start of the study. Method of measurement: Pittsburgh Sleep Quality Index.;Intensity of anxiety. Timepoint: Filling out the questionnaire will be done at the beginning of the study (before the intervention) and 30 days after the start of the study. Method of measurement: Beck Anxiety Inventory.;Mother-infant relationship quality. Timepoint: Filling out the questionnaire will be done at the beginning of the study (before the intervention) and 30 days after the start of the study. Method of measurement: Parent-ChildBonding Instrument. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSeyed Mohammad Javad Mousavi
Boushehr University of Medical Sciences
Outcome results
None listed