RecruitingNot ApplicableNCT06698107

Salutogenesis and Self-efficacy-based Childbirth Education Programme for Preventing Postpartum Depression

Effectiveness of Childbirth Education Based on Salutogenic Perspective and Self-Efficacy Theory in Preventing Postpartum Depression Among Ethiopian Teenage Mothers: a Pilot RCT Study


Sponsor

The Hong Kong Polytechnic University

Enrollment

130 participants

Start Date

Dec 5, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Although the transition to motherhood is often a joyful experience, there is evidence that teenage motherhood can present many stressful challenges, potentially leading to the development of postpartum depression. Postpartum depression (PPD) remains a public health issue with negative consequences for both mothers and their babies. The aim of this study is to assess the feasibility of implementing childbirth education underpinned by salutogenic and self-efficacy perspectives among teenage mothers in low-income settings. The study also aims to provide preliminary findings on the intervention's effectiveness in preventing postpartum depression among Ethiopian teenage mothers. The theoretical based childbirth education approach can enhance the psychosocial well-being of first-time teenage mothers. The intervention consists of six sessions: three during the antenatal period and three in the postpartum period. These sessions contain two individual face-to-face educations (each lasting 60-90 minutes), two phone calls (each lasting 30 minutes), and two group discussion (each lasting 90-120 minutes), as supported by the existing evidence. The study expected to support the feasibility of the study design. Preliminary findings are anticipated to show a significant difference in postpartum depression scores between the intervention and control groups, with teenage mothers in the intervention group having a lower risk of postpartum depression compared to those in the control group. Integrating sense of coherence and self-efficacy theories into maternity care services could provide empirical support for preventive efforts against postpartum depression. The findings of this study may address research gaps regarding the psychosocial wellbeing of teenage mothers, serving as baseline evidence for large scale interventional studies that consider the sociocultural and economic contexts of low-income countries.


Eligibility

Sex: FEMALEMin Age: 13 YearsMax Age: 19 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether a special childbirth education program focused on building confidence and resilience can reduce the risk of postpartum depression in young, first-time mothers. **You may be eligible if...** - You are a married first-time mother between 13 and 19 years old - You are 28–30 weeks pregnant with a single baby - You have no complications that would prevent a vaginal delivery - You plan to give birth and have follow-up appointments at a participating hospital - You will be living near the participating hospital for at least 12 weeks after delivery **You may NOT be eligible if...** - You have a history of mental health problems or are currently experiencing them - You have participated in a similar educational program before - You have serious medical or obstetric complications Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

BEHAVIORALChildbirth education programme

The intervention framework is underpinned by a converging of salutogenic and self-efficacy perspectives, aiming to enhance mothers' ability to adapt to new motherhood life despite stressors, and to address the question, "How do teenage mothers stay well despite stressful events of transition to motherhood?" The intervention consists of six sessions: three of which will be provided in the antenatal period and the other three in the postpartum period. The sessions contain two individual face-to-face educations (each lasting 60-90 minutes), two phone calls (each lasting 30 minutes), and two group discussion sessions (each lasting 90-120 minutes), as supported by the existing evidence.

OTHERUsual Care

The control group will receive the usual maternity care.


Locations(4)

Addis Alem Hospital

Bahir Dar, Amhara, Ethiopia

Felege Hiwot Specialized Hospital

Bahir Dar, Amhara, Ethiopia

Tibebe Gion Hospital

Bahir Dar, Amhara, Ethiopia

Dessie Specialized Hospital

Dessie, Amhara, Ethiopia

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NCT06698107


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