TrueBlue Clinical Study - Investigating the Use of a Mobile Phone App TrueBlue for Monitoring Depression and Anxiety

Recruiting now · Not applicable

Conditions studied: Depression, Depression, Postpartum, Anxiety in Pregnancy, Anxiety, Anhedonia, Perinatal Depression

In brief

This trial will assess the safety, feasibility, acceptability, usability and agreement with validated scales of an automated mood monitoring App (TrueBlue), in adult, perinatal participants (recruited between 12 weeks of pregnancy and 12 weeks post-partum), recruited across multiple sites in Nottinghamshire, United Kingdom (UK). An initial within-study pilot phase will assess key aspects of the study including recruitment rate, usability issues and a detailed understanding of any device related adverse events; prior to full recruitment of a total 125 participants over a total 14-month period.

Key facts

Study ID
NCT06364488
Run by
BlueSkeye AI
People needed
125
Starts
2024-10-01
Expected to finish
2026-12-30
Last updated by the study team
2025-09-19

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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