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Clinical Trials in Spain / NCT06442774
Recruiting Not applicable

MamaConecta: Digital Tool for Maternal Mental Health

NCT06442774 · tracked via the Priya Life Science Spain tracker
Sponsor
A Thousand Colibris, S.L
Phase
Not applicable
Started
2024-12-28
Last updated
2025-01-17

Condition(s) studied

Pregnancy RelatedMental Health IssuePostpartum DepressionPostpartum AnxietyWell-Being, Psychological

Investigational drug(s) / intervention(s)

Mobile applicationMonitoring via wearable

Mobile application: The intervention that has been developed is a digital tool of a biopsychosocial nature based on the main cognitive-behavioral strategies: psychoeducation, reflection, self-observation, guided visualizations, mindfulness and progressive muscle relaxation. The intervention consists of 3 main areas of work: * Programs: Biopsychosocial programs in text and audio format. * Community: Forum with directed questions and space to share experiences between mothers. * Diary: Space to record mood and emotional record. The entire tool works transversally in 4 dimensions: self-care, relationship with perinatal changes, relationship with the baby, social relationship. The tool itself includes 3 mental health and well-being screening questionnaires: Whooley Questionnaire and the Edinburgh Postnatal Depression Scale (EPDS).

Monitoring via wearable: Participants that own a wearable will connect it to monitor variables related to sleeping patterns, activity and stress (see variables section).

Study summary

The goal of this randomized controlled trial is to validate a digital health tool, Dana app, that enhances well-being and supports mental health monitoring for women during the perinatal period. The primary purpose is to improve maternal well-being, early detection of mental health issues, and aid in the diagnosis and monitoring by healthcare professionals in women transitioning into motherhood. The main questions it aims to answer are:

* Does the app improve overall maternal well-being during the perinatal period?
* Can the app increase the early detection rates of perinatal mental health disorders?
* Can the app be an effective tool to support healthcare professionals to diagnose perinatal mental health problems?
* How effective is the app in improving obstetric outcomes and the psychological and cognitive development of infants?

Researchers will compare the group using the app with a control group not using the digital tool to see if Dana provides significant improvements in maternal and infant health outcomes.

Participants will:

* Use the mobile application from 12-14 weeks of gestation until 24 months postpartum.
* Undergo regular assessments to monitor their emotional state, lifestyle, clinical, and obstetric data.
* Participate in evaluations for their infants' psychological and cognitive development at various stages from birth to two years old.

This trial is conducted at multiple centers, including Hospital Vall d'Hebron, the Sexual and Reproductive Health Care Services (ASSIR) in Tarragona and ASSIR Litoral (Barcelona), Hospital del Mar, following CONSORT standards. The study aligns with the Health and Culture priorities of the Spanish Government's Scientific, Technical, and Innovation Research Plan 2021-2023.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Gestational age between 12-14 weeks of gestation. * The first obstetric ultrasound has been performed. * Women who know how to read and understand Spanish. * Women who have access to a mobile phone with an internet connection (data or wifi) * Women who have knowledge of technology tools via app. * Have signed the informed consent to participate in the study. Exclusion Criteria: * Termination of pregnancy, or early miscarriage * Perinatal loss at any time during pregnancy. * Severe mental pathology or moderate unstable mental pathology. * Consumption of toxic substances.

Primary outcome measure(s)

Trial sites (3)

FacilityCityRegionStatus
Hospital Vall d'Hebron Barcelona Catalonia Recruiting
Hospital del Mar Barcelona Spain Recruiting
ASSIR Tarragona Tarragona Spain Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06442774 on ClinicalTrials.gov ↗ ← All trials in Spain