Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT06512025

Implementation of a Psychoeducational Intervention in New Mothers

Led by Alba Roca · Updated on 2025-02-26

400

Participants Needed

2

Research Sites

133 weeks

Total Duration

On this page

Sponsors

A

Alba Roca

Lead Sponsor

F

Fundació La Marató de TV3

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to implement and examine the clinical effectiveness in a randomized study of the Catalan and Spanish versions of the culturally adapted "What Were We Thinking (WWWT)" psychoeducational intervention in primary care services, with the aim of preventing and reducing the prevalence of postpartum mental illness in new mothers. Additionally, the trial will assess the acceptability and accessibility of the intervention by families and professionals. Researchers will compare "Usual Care" (standard postnatal care provided by professionals from the Sexual and Reproductive Health Service) with "Intervention group" (usual care plus two psychoeducative intervention WWWT sessions) to see if the "WWWT intervention" is better than "Usual Care" at preventing postpartum depression and anxiety disorders in new mothers. Participants will: * Take baseline questionnaires at 2-4 weeks postpartum * Take usual care or usual care plus two psychoeducative intervention WWWT sessions within the first 6 weeks postpartum * Take the same questionnaires used in baseline plus a semi-structured interview to diagnose major mental disorder (all participants) at 3 and 6 months follow-up * Take a brief anonymous self-report survey (only those participants taking the WWWT intervention)

CONDITIONS

Official Title

Implementation of a Psychoeducational Intervention in New Mothers

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Primiparous women
  • Given birth to a healthy, full-term baby in the preceding 2 weeks
  • Receiving postpartum healthcare at Atenci�f3 a la salut sexual i reproductiva (ASSIR) of �c0rea Integral de Salut Barcelona Esquerra (AIS-BE)
  • Over 18 years of age
  • Give consent to participate in the study
Not Eligible

You will not qualify if you...

  • Unable to complete the questionnaires due to language or literacy barriers

AI-Screening

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Trial Site Locations

Total: 2 locations

1

Unitat de Salut Mental Perinatal (USMP) de l'Hospital Clínic de Barcelona

Barcelona, Barcelona, Spain, 08036

Not Yet Recruiting

2

Atenció a la salut sexual i reproductiva (ASSIR) de l'Àrea Integral de Salut Barcelona Esquerra (AIS-BE)

Barcelona, Barcelona, Spain

Actively Recruiting

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Research Team

A

Alba Roca, Doctor

CONTACT

N

Noelia Fernández, Graduate

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

NA

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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