HappyMums Mobile Application Study
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorKing's College London
About this trial
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.
Eligibility criteria
Qualifiers
Pregnant people, aged 18 or older and up to 28 weeks' gestation.
Satisfactory understanding of English/national language of host country, in order to give fully informed consent.
Either suffering with depressive symptoms currently, or who have at least one risk factor for antenatal depression.
Owning a smartphone capable of downloading and running HappyMums application
Disqualifiers
Inability to give informed consent.
Trial design
Treatments tested in this trial
- Not listed
Trial groups
1,000 Participants
are grouped into 1 trial groupSponsors and collaborators
King's College London
Lead sponsor
University of Milan
Collaborator
Ospedale San Raffaele
Collaborator
Catholic University of Croatia
Collaborator
University of Helsinki
Collaborator
Charite University, Berlin, Germany
Collaborator
SWPS University of Social Sciences and Humanities
Collaborator
Ab.Acus
Collaborator
University of Barcelona
Collaborator
Source ClinicalTrials.gov