← Back to Clinical Trials
Recruiting NCT07609550

NCT07609550 Feasibility and Implementation of Early Referral in Perinatal Mental Health

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07609550
Status Recruiting
Phase
Sponsor University of Seville
Condition Perinatal Depression
Study Type INTERVENTIONAL
Enrollment 3,000 participants
Start Date 2026-07-15
Primary Completion 2027-12-30

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
The e-Perinatal intervention is a personalized mobile health (mHealth) programStandard routine maternal care

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 3,000 participants in total. It began in 2026-07-15 with a primary completion date of 2027-12-30.

⚠ 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

This study is part of the e-Perinatal project and is embedded within the main cluster randomized trial. The primary aim is to evaluate the feasibility, acceptability, and preliminary effectiveness of an early diagnosis detection and referral strategy to specialized mental health services within routine maternal care. The secondary aim is to validate and implement an Artificial Intelligence-based algorithm for the early screening of mental health disorders in routine services.

Eligibility Criteria

Inclusion Criteria: * Pregnant and postpartum women enrolled in the main e-Perinatal trial, indicating the presence of a depressive or anxiety disorder with CIDI. * Access to smartphone and internet * Able to write and read in Spanish Exclusion Criteria: * None beyond those defined in the main trial

Contact & Investigator

Central Contact

Emma Motrico, PhD

✉ eperinatal@us.es

📞 0034636995778

Principal Investigator

Emma Motrico, PhD

PRINCIPAL INVESTIGATOR

University of Seville

Frequently Asked Questions

Who can join the NCT07609550 clinical trial?

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

Is NCT07609550 currently recruiting?

Yes, NCT07609550 is actively recruiting participants. Contact the research team at eperinatal@us.es for enrollment information.

Where is the NCT07609550 trial being conducted?

This trial is being conducted at Mairena del Aljarafe, Spain.

Who is sponsoring the NCT07609550 clinical trial?

NCT07609550 is sponsored by University of Seville. The principal investigator is Emma Motrico, PhD at University of Seville. The trial plans to enroll 3,000 participants.

Related Trials

Related Intelligence Guides

In-depth guides covering this condition's trials, eligibility, and what to expect.

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: September 2026  ·  Data Methodology