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

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

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170506033834N11
Enrollment
93
Registered
2023-08-20
Start date
2023-09-06
Completion date
Unknown
Last updated
2023-10-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postpartum. Z39

Interventions

Intervention 1: Intervention group: In one of the intervention groups, supportive counseling will be done at home during three sessions on days 5-3 7-9 and 20-25 after delivery for 30-45 minutes .The

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

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

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...

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactbita eskandari

Tabriz University of Medical Sciences

bitaeskandari7250@gmail.com+98 41 3479 6770

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026