Actively Recruiting
Maternal Well-being in the Postnatal Stage
Led by Universidad Complutense de Madrid · Updated on 2025-05-21
98
Participants Needed
1
Research Sites
162 weeks
Total Duration
On this page
Sponsors
U
Universidad Complutense de Madrid
Lead Sponsor
U
Universidad Pontificia de Salamanca
Collaborating Sponsor
AI-Summary
What this Trial Is About
The objective of this study is to design and validate an online intervention aimed at promoting well-being in women with postpartum depression. For this, the design of a multicomponent protocol consisting of empirically validated positive interventions and comparing these with a group Cognitive Behavioral Therapy (CBT) is proposed, following the National Institute for Health and Care Excellence (NICE) recommendations for the treatment of depression. Participants will be screened for inclusion in the program if they meet clinical criteria. After that, they will be randomly assigned to a CBT group or a positive psychology intervention (PPI) group.
CONDITIONS
Official Title
Maternal Well-being in the Postnatal Stage
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women who have been mothers in the last year
You will not qualify if you...
- Women who have been mothers in the last month
- Women who meet the Diagnostic and Statistical Manual of Mental Disorders (DSM-5) criteria for substance abuse and/or dependence within 30 days prior to study participation
- Women who have a serious mental disorder that makes it difficult to follow the protocol (e.g. serious neurocognitive problems or brain damage; schizophrenia and other psychotic disorders).
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Covadonga Chaves Vélez
Madrid, Pozuelo de Alarcón, Spain, 28223
Actively Recruiting
Research Team
C
Covadonga Chaves
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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