Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
Healthy Volunteers
ID06787300

The Effect of Stories That Empower Mothers Programme on Postpartum Depression in First-Time Pregnant Women

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

This research focuses on postpartum depression, a challenging condition that affects mothers after childbirth. Pregnant women experiencing their first pregnancy are studied to assess their risk of postpartum depression and to explore ways to prevent it. The study evaluates a specially created program called 'Stories to Empower Mothers,' designed by psychiatric nurses, psychotherapists, and art therapists to support mental health during pregnancy and reduce postpartum depression risk. The program includes six sessions, with the first held face-to-face and the remaining five conducted online. It uses art therapy techniques such as imagery, painting, and story writing to help mothers explore self-knowledge, identify difficulties and strengths, and develop new coping strategies. Participants create a storybook reflecting their journey through the sessions. The intervention is compared to a control group in a non-randomized experimental design. Participants attend assessments at multiple times: before the program (24-32 gestational weeks), after five weeks, and postpartum at 2-4 weeks and 10-12 weeks. Researchers collect data through forms and validated scales measuring depression and psychological resilience. The study monitors participant progress, adherence to sessions, and collects artwork photos to evaluate the program's impact on postpartum depression risk and resilience.

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

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Research Team

E

Ege M Topcu, Research Asst.

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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