Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
Healthy Volunteers
NCT06787300

Stories That Empower Mothers and Postpartum Depression

Led by Ege University · Updated on 2025-01-22

30

Participants Needed

1

Research Sites

239 weeks

Total Duration

On this page

Sponsors

E

Ege University

Lead Sponsor

T

The Scientific and Technological Research Council of Turkey

Collaborating Sponsor

AI-Summary

What this Trial Is About

Postpartum depression is a condition that occurs after birth and is difficult for mothers. Research shows that experiencing postpartum depression once increases the risk of experiencing it in subsequent pregnancies. At the same time, there are findings in the literature that pregnant women with postpartum depression experience mental difficulties, anxiety or depression during pregnancy. For this reason, this study aims to determine the risk of postpartum depression in pregnant women who are pregnant for the first time during pregnancy and to prevent this risk from occurring in the postpartum period. For this purpose, 'Stories to empower mothers' programme was created. This programme was created by researchers who are specialist psychiatric nurses, psychotherapists and art therapists and finalised with expert opinions. The programme consists of six sessions. The sessions are individual and are conducted online except for the first session. A storybook is formed at the end of the programme with the steps followed during the sessions. While creating this storybook, the themes of self-knowledge, defining the situation, identifying difficulties, identifying sources of help, discovering strengths and creating new coping strategies are addressed by using art therapy techniques. The aim of the study is to examine the effect of the 'Stories Empowering Mothers Programme' on the risk of postpartum depression in pregnant women experiencing their first pregnancy. The research is conducted in a non-randomised experimental follow-up research design. Pregnant women who meet the inclusion criteria of the study can be included in the experimental or control group according to their wishes. The data collection process in the study proceeds in the order of determining the target group, pre-test (24-32nd gestational week), post-test (after 5 weeks), follow-up one test (postpartum 2nd-4th week) and follow-up two tests (postpartum 10th-12th week). The data are obtained with the Case Report Form and Postpartum Information Form prepared by the researcher and EPDI, BDI and Brief Psychological Resilience Scale forms. Expert support will be obtained for statistical analyses. Ethics committee permission was obtained before the research was started to be conducted. The research is a doctoral thesis supported by TÜBİTAK.

CONDITIONS

Official Title

Stories That Empower Mothers and Postpartum Depression

Who Can Participate

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • First pregnancy
  • Singleton pregnancy
  • Gestational week between 24 and 32
  • Regular doctor follow-up
  • Scored 10 or higher on the Edinburgh Postnatal Depression Scale
  • Scored less than 17 on the Beck Depression Inventory
  • Literate
  • No sensory disabilities preventing communication
  • Own a smartphone or computer
  • Have internet access
  • Volunteer to participate
Not Eligible

You will not qualify if you...

  • Currently in the first trimester of pregnancy
  • Receiving treatment for any psychiatric diagnosis
  • Having a risky pregnancy
  • At risk of premature birth or already developed premature birth
  • Experiencing pregnancy complications like gestational diabetes, hypertension, or bleeding
  • Baby is not healthy
  • Developing complications during or after birth
  • Baby requires intensive care after birth
  • Have experienced loss of a baby
  • Had a premature birth before 37 weeks
  • Mother has faced serious daily life difficulties such as disasters or losses
  • Missing three or more of the six program sessions

AI-Screening

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Trial Site Locations

Total: 1 location

1

Ege University

Izmir, Turkey (Türkiye), 35100

Actively Recruiting

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Research Team

E

Ege M Topcu, Research Asst.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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