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Mobile Sensing and Support for Depression — MOSS  

Depression Clinical Trial

Official title:
Monocentric Study for Development of a Smartphone Application for Patients With Depressive

Clinical Trial Summary

The objective of this study is two fold, first to explore the potential of context sensitive intervention delivery to provide in-situ support for people with depressive symptoms, second to explore the detection of daily-life behavior based on smart phone sensor information to identify subjects with a clinically meaningful depression level.

Clinical Trial Description

To conduct a very first pilot trial, a monocentric, single-arm clinical study is conducted. The study is approved by the local ethics committee of the Canton of Zurich in Switzerland and the Swiss Agency for Therapeutic Products. It is conducted in full accordance with the Declaration of Helsinki, with all subjects providing their electronic informed consent prior to participation. As the main interest lies in a proof of concept of the proposed MOSS app, emphasis is put on real life conditions. A range of different recruitment channels is used to attract subjects from the general public; they include physical flyers, online posts on relevant online bulletin boards and the Google Play Store. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02776839
Study type Interventional
Source University of Zurich
Contact
Status Completed
Phase N/A
Start date March 2015
Completion date December 2015
View Details
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