Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
ID06512025

Adaptation and Implementation of a Psychoeducational Intervention to Prevent Postpartum Depression and Anxiety Disorders in New Mothers

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

400

Participants Needed

2

Research Sites

N/A

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

Researchers are evaluating the effectiveness of the culturally adapted Catalan and Spanish versions of the "What Were We Thinking (WWWT)" psychoeducational intervention in preventing and reducing postpartum mental illness in new mothers. This randomized study compares the standard postnatal care ("Usual Care") with the usual care plus two WWWT sessions to see if the intervention better prevents postpartum depression and anxiety disorders. The trial also assesses how acceptable and accessible the intervention is to families and healthcare professionals. Participants are assigned to either receive the usual postpartum care provided by the Sexual and Reproductive Health Service (ASSIR) or the usual care plus two structured WWWT psychoeducational sessions within the first six weeks after giving birth. The WWWT program is designed for small groups of 5-7 families and includes mothers, partners or other caregivers, and infants. Each session lasts two hours and focuses on promoting confident parenting, improving partner relationships, and managing infant care. During the study, participants complete baseline questionnaires between two and four weeks postpartum. Follow-up assessments, including the same questionnaires and a semi-structured interview to diagnose major mental disorders, take place at three and six months postpartum. Additionally, those in the intervention group complete a brief anonymous satisfaction survey after the WWWT sessions. Researchers measure mental disorders, depressive and anxiety symptoms, maternal bonding, parenting self-regulation, and marital adjustment throughout the study period.

CONDITIONS

Brief 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

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Up to 6 weeks postpartum

Participants attend two psychoeducative intervention sessions designed for groups of families within the first 6 weeks postpartum.

2 sessions (in-person)

Follow-up

Duration - 6 months postpartum

Participants are followed up to assess mental health, maternal bonding, parenting self-regulation, and marital adjustment.

3 visits at baseline, 3 months, and 6 months postpartum

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

N

Noelia Fernández, Graduate

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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