Psychoeducational Intervention to Reduce Depressive Symptoms and Strengthen Mother-Infant Bonding

NCT07062159 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 88

Last updated 2026-01-07

No results posted yet for this study

Summary

The study aims to evaluate the effectiveness of a psychoeducational intervention designed within the framework of the Watson Human Caring Model in reducing postpartum depressive symptoms and creating a stronger mother-infant bond. Specifically, it aims to investigate whether a person-centered approach based on the principles of Watson's caring science can significantly increase the psychological well-being of postpartum mothers and improve the quality of their relationship with their babies.

Conditions

Interventions

OTHER

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.

OTHER

routine care

routine care

Sponsors & Collaborators

  • Yasemin Ozhuner

    lead OTHER

Principal Investigators

  • Yasemin Özhüner · Eskişehir Vadişehir Family center odunpazarı Turkey

  • Nebahat Ozerdogan · Eskisehir Osmangazi University odunpazarı turkey

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-07-02
Primary Completion
2025-08-19
Completion
2026-01-05

Countries

  • Turkey (Türkiye)

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07062159 on ClinicalTrials.gov