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Recruiting NCT05676918

NCT05676918 Maternal Well-being in the Postnatal Stage

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Clinical Trial Summary
NCT ID NCT05676918
Status Recruiting
Phase
Sponsor Universidad Complutense de Madrid
Condition Postpartum Depression
Study Type INTERVENTIONAL
Enrollment 98 participants
Start Date 2023-01-16
Primary Completion 2025-06-01

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Positive Psychology InterventionCognitive Behavior Therapy

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 98 participants in total. It began in 2023-01-16 with a primary completion date of 2025-06-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: * Women who have been mothers in the last year Exclusion Criteria: * 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).

Contact & Investigator

Central Contact

Covadonga Chaves

✉ cchavesv@psi.ucm.es

📞 +34635321643

Principal Investigator

Covadonga Chaves, PhD

PRINCIPAL INVESTIGATOR

Universidad Complutense de Madrid

Frequently Asked Questions

Who can join the NCT05676918 clinical trial?

This trial is open to female participants only, aged 18 Years or older, studying Postpartum Depression. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05676918 currently recruiting?

Yes, NCT05676918 is actively recruiting participants. Contact the research team at cchavesv@psi.ucm.es for enrollment information.

Where is the NCT05676918 trial being conducted?

This trial is being conducted at Madrid, Spain.

Who is sponsoring the NCT05676918 clinical trial?

NCT05676918 is sponsored by Universidad Complutense de Madrid. The principal investigator is Covadonga Chaves, PhD at Universidad Complutense de Madrid. The trial plans to enroll 98 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology