Actively Recruiting
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
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
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
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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