Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT05676918

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

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women who have been mothers in the last year
Not Eligible

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

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Covadonga Chaves Vélez

Madrid, Pozuelo de Alarcón, Spain, 28223

Actively Recruiting

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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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