Comparison of the effect of in-home and phone supportive counseling on postpartum depression and anxiety: a randomized controlled clinical trial

Not Applicable

Recruiting

Conditions: Postpartum.
Z39
Encounter

Registration Number: IRCT20170506033834N11

Lead Sponsor: Tabriz University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: Female

Target Recruitment: 93

Inclusion Criteria

Primiparous women by vaginal method
Having a desire to breastfeed
Age 18-45
Living in Tabriz
Single birth
Mothers with term babies weighing 2500 to 4000 grams

Exclusion Criteria

Mothers with hospitalized babies.
Existence of systemic and chronic diseases or aggravating disorders during pregnancy and childbirth, including gestational or overt diabetes, blood pressure disorders, heart disease, and the inability of the mother to care for the baby.
Breast anomaly or history of breast surgery
The existence of unfortunate events in the last three months, including the death of loved ones, divorce, etc.
Obtaining a depression score of 13 or more based on the Edinburgh postpartum depression scale
Depressive disorders before pregnancy and delivery according to mother's statement
Cases of malformation and infant death
Excessive bleeding during childbirth
Having breast-feeding contraindications (women undergoing chemotherapy, women with HIV infection, women with untreated active tuberculosis, and the use of radioactive, antimetabolite and illegal drugs during breastfeeding such as methotrexate, mercaptopurine, hydroxyurea, tamoxifen, bromocriptine, Lithium, phenin-dione, phen-cyclidine, cyclophosphamide and doxorubicin, drugs and...

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postpartum Depression. Timepoint: 10-15 days and 42-60 days after delivery by controlling the effect of baseline score. Method of measurement: Edinburgs Postpartum Depression Scale.;Specific postpartum anxiety. Timepoint: 10-15 days and 42-60 days after delivery by controlling the effect of baseline score. Method of measurement: PSAS-RSF(Postpartum Specific Anxiety Scale Research short-form).

Secondary Outcome Measures

Name	Time	Method
Quality of life of mothers. Timepoint: 10-15 days after delivery. Method of measurement: MAPP-QOL(Maternal Postpartum Quality).;Frequency of exclusive breastfeeding. Timepoint: 42-60 days after birth. Method of measurement: A checklist designed to record breastfeeding status.;Comparison of infant weight. Timepoint: One month after giving birth. Method of measurement: Baby weight card.;Comparison of the frequency of newborn visits by doctors. Timepoint: 42-60 days after birth. Method of measurement: Checklist designed to record the number of baby visits by the doctor.