Psychoeducatıon Interventıon Postpartum Depressıon Breastfeedıng

NCT ID: NCT06779903

Last Updated: 2025-03-11

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 102 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-11-13
• Study Completion Date: 2025-03-01

Brief Summary

This study was planned to evaluate the effects of psychoeducation intervention for postpartum care on postpartum depression and breastfeeding.

Detailed Description

The pregnant women included in the sample were informed about the study and their written informed consent was obtained. Six interviews were conducted with the pregnant women, four at one-week intervals before birth, and one on the tenth day and sixth week after birth. These interviews were conducted with the women one-on-one and face-to-face.Women in the control group were not given any treatment other than routine care at family health centers. The psychoeducation program was applied to the women in the intervention group in six interviews.

Conditions

Postpartum Depression; Psychoeducation; Breastfeeding; Postpartum Care

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: SINGLE

Study Groups

intervention group

The pregnant women included in the sample were informed about the study and their written informed consent was obtained. Six interviews were conducted with the pregnant women, four at one-week intervals before birth, and one on the tenth day and sixth week after birth. These interviews were conducted with the women one-on-one and face-to-face. psychoeducation program was applied to the women in the intervention group in six interviews.In the first interview, the psychoeducation intervention program booklet based on the Watson Model for postpartum care was given to the women and the interview was conducted within the scope of the program. The psychoeducation intervention program sessions based on the Watson Model for postpartum care in the study were conducted according to the WİBM improvement processes and psychoeducation techniques. The interviews lasted between 90 and 120 minutes on average.

Group Type: ACTIVE_COMPARATOR

the psychoeducation intervention program booklet

Intervention Type: OTHER

Psychoeducation Program was composed of nine basic topics (postpartum period and care, adaptation to the role of motherhood and mother-infant bonding, postpartum psychological changes, frequency, causes, symptoms of PPD, effects on mother, child and community health, diagnosis and treatment, preventive practices, social support and suggestions for coping, breast milk and breastfeeding, breast care and practices, nutrition and baby care).

control group

The pregnant women included in the sample were informed about the study and their written informed consent was obtained. Six interviews were conducted with the pregnant women, four at one-week intervals before birth, and one on the tenth day and sixth week after birth. These interviews were conducted with the women one-on-one and face-to-face.Women in the control group were not given any treatment other than routine care at family health centers. In routine care, pregnant women were subjected to edema, varicose veins, weight, blood pressure, pulse, laboratory findings, baby heart sounds, medication intake, chronic disease follow-up and vaccination. Pregnant women were provided with counseling if they had any questions. Postpartum women were subjected to blood pressure, fever, pulse, bleeding and laboratory findings follow-up and were provided with counseling if they had any questions.

Group Type: PLACEBO_COMPARATOR

routine care

Intervention Type: OTHER

routine care

Interventions

the psychoeducation intervention program booklet

Psychoeducation Program was composed of nine basic topics (postpartum period and care, adaptation to the role of motherhood and mother-infant bonding, postpartum psychological changes, frequency, causes, symptoms of PPD, effects on mother, child and community health, diagnosis and treatment, preventive practices, social support and suggestions for coping, breast milk and breastfeeding, breast care and practices, nutrition and baby care).

Intervention Type: OTHER

routine care

routine care

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• 20-34. Women who are at the gestational age,
• over 18 years of age,
• planning to breastfeed,
• have no visual,
• hearing or mental disabilities,
• have a healthy fetus on ultrasonography

Exclusion Criteria

• Women with depression and other mental illnesses diagnosed by a physician,
• those taking medication related to their mental illness,
• those who gave birth prematurely,
• those with contraindications to breastfeeding and newborns (head and spine anomalies such as anencephaly/spina bifida, having a fetus with brain anomalies such as hydrocephalus/microcephaly, active substance use or HIV diagnosis, etc.),
• those who were included in the study in the 3rd trimester but whose birth weight was less than 2500 grams,
• those whose babies were taken to the neonatal intensive care unit due to any postpartum complications and those who had premature babies (born before 37 weeks of gestation),
• those who did not participate in more than one interview

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 45 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

Eskisehir Osmangazi University

OTHER

Sponsor Role: lead

Responsible Party

Yasemin Ozhuner

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Yasemin Özhüner

Role: PRINCIPAL_INVESTIGATOR

Eskişehir Vadişehir Family center odunpazarı Turkey

nebahat özerdoğan

Role: STUDY_DIRECTOR

Eskisehir Osmangazi University odunpazarı turkey

Locations

Eskisehir Osmangazi University

Eskişehir, Odunpazarı, Turkey (Türkiye)

Countries

Turkey (Türkiye)

Other Identifiers

PSYCHOEDUCATION DEPRESSION

Identifier Type: -

Identifier Source: org_study_id