Feasibility and Implementation of Early Referral in Perinatal Mental Health
Recruiting
N/A
Interventional Study
Perinatal Depression
Perinatal Anxiety
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 3,000 (estimated)
- Sponsor
- University of Seville · Other
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About This Trial
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 a…
Trial Locations
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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 tr…
Contacts