Actively Recruiting
HappyMums Mobile Application Study
Led by King's College London · Updated on 2025-12-09
1000
Participants Needed
7
Research Sites
88 weeks
Total Duration
On this page
Sponsors
K
King's College London
Lead Sponsor
U
University of Milan
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this study is to investigate whether pregnant people at risk of, or currently suffering from antenatal depression, find it acceptable to use the 'HappyMums' mobile application during their pregnancy. This app will collect data relevant to their mental health passively and through active engagement from the user. After the study is complete, these data will be put together to determine if such data types could be used in future to help predict and identify antenatal depression, and aid better treatment decisions.
CONDITIONS
Official Title
HappyMums Mobile Application Study
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pregnant people aged 18 years or older and up to 28 weeks' gestation
- Good understanding of English or the national language to provide informed consent
- Currently experiencing depressive symptoms or having at least one risk factor for antenatal depression
- Owning a smartphone capable of downloading and running the HappyMums application
You will not qualify if you...
- Unable to give informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 7 locations
1
Catholic University of Croatia
Zagreb, Croatia
Actively Recruiting
2
University of Helsinki
Helsinki, Finland
Actively Recruiting
3
Charité - Universitätsmedizin Berlin
Berlin, Germany
Actively Recruiting
4
San Raffaele Hospital
Milan, Italy
Actively Recruiting
5
University of Milan
Milan, Italy
Actively Recruiting
6
SWPS University
Warsaw, Poland
Actively Recruiting
7
King's College London
London, UK, United Kingdom, SE5 9RX
Actively Recruiting
Research Team
A
Anthony J Woods, PhD
CONTACT
C
Carmine M Pariante, MD, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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