Actively Recruiting
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
Eligibility Criteria
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
You will not qualify if you...
- Unable to complete the questionnaires due to language or literacy barriers
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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)
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
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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