Psychoeducational Intervention to Reduce Depressive Symptoms and Strengthen Mother-Infant Bonding
NCT ID: NCT07062159
Last Updated: 2026-01-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
88 participants
INTERVENTIONAL
2025-07-02
2026-01-05
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
intervention group (44)
Study Groups
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intervention group
Active Comparator: intervention group The pregnant women in the sample were informed about the study and their written consent was obtained. A total of six interviews were conducted with the pregnant women, four at one-week intervals before birth and one interview on the seventh day and fourth week after birth. These interviews were conducted with the women one-on-one and face-to-face. The psychoeducation program was applied to the women in the intervention group in six interviews. In the first interview, the women were given a booklet of the psychoeducation intervention program based on the Watson Human Caring Model for postpartum care and the interview was conducted within the scope of the program. The psychoeducation intervention program interviews based on the Watson Human Caring Model in the study were conducted according to the Watson Human Caring Model improvement processes and psychoeducation techniques. The interviews lasted between 60-90 minutes on average.
the psychoeducation intervention program
The content of the psychoeducation intervention program based on the Watson Human Caring Model will consist of the postpartum process and care, maternal blues, postpartum psychosis, postpartum depression, frequency, causes, predisposing factors, symptoms, effects on mother, child and community health, diagnosis and treatment, preventive practices, social support, adaptation to the role of motherhood, mother and baby bonding, practices that will strengthen mother-baby bonding, breast milk and breastfeeding, nutrition and baby care, problems encountered in baby care and solution suggestions.
control group
Placebo Comparator: Control Group The pregnant women in the sample were informed about the study and their written consent was obtained. Six interviews were conducted with the pregnant women, four at one-week intervals before delivery and once on the seventh day and fourth week after delivery. These interviews were conducted with the women one-on-one and face-to-face. The women in the control group did not receive any treatment other than their routine care at family health centers. In routine care, pregnant women were examined for 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. After delivery, women were provided with medication intake, blood pressure, fever, pulse, bleeding and laboratory findings and counseling if they had any questions.
routine care
routine care
Interventions
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the psychoeducation intervention program
The content of the psychoeducation intervention program based on the Watson Human Caring Model will consist of the postpartum process and care, maternal blues, postpartum psychosis, postpartum depression, frequency, causes, predisposing factors, symptoms, effects on mother, child and community health, diagnosis and treatment, preventive practices, social support, adaptation to the role of motherhood, mother and baby bonding, practices that will strengthen mother-baby bonding, breast milk and breastfeeding, nutrition and baby care, problems encountered in baby care and solution suggestions.
routine care
routine care
Eligibility Criteria
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Inclusion Criteria
* Volunteers,
* Over 18 years of age,
* Literate,
* No visual, hearing or mental disabilities,
* Having a healthy baby weighing over 2500 grams,
* Being in the same environment with their baby after birth,
* Having a healthy fetus on ultrasound will be included in the study.
Exclusion Criteria
* Those taking medication for mental illness,
* Women who have given birth prematurely,
* Stillbirth,
* Those who have not participated in more than one interview will not be included in the study.
18 Years
FEMALE
Yes
Sponsors
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Yasemin Ozhuner
OTHER
Responsible Party
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Yasemin Ozhuner
DR
Principal Investigators
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Yasemin Özhüner
Role: PRINCIPAL_INVESTIGATOR
Eskişehir Vadişehir Family center odunpazarı Turkey
Nebahat Ozerdogan
Role: STUDY_DIRECTOR
Eskisehir Osmangazi University odunpazarı turkey
Locations
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Eskisehir Osmangazi University
Eskişehir, Odunpazarı, Turkey (Türkiye)
Countries
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Other Identifiers
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Attachment and depression
Identifier Type: -
Identifier Source: org_study_id
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