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Acceptability Study by Patients Admitted for Suicide and by Medical Staff for Clinical Data Collection Through an E-health Platform — MeMind  

Suicide, Attempted Clinical Trial

Official title:
Acceptability Study SMARTphone to Collect Clinical Data Using the Memind App by Patients and Medical Satff.

Clinical Trial Summary

The study goal is to determine the feasbility and interest of monitoring mental health and non mental health related simptoms in Outpatients in order to prevent suicide.

Clinical Trial Description

Taking into account the strengths and pitfalls of existing suicide risk assessment methods, we have designed a system capable to combine EMA and continuous monitoring of patients using the smartphone's and/or wearable's sensors and data entry in order to monitor and predict suicide risk. For example, both poor sleep quality and disturbed appetite are clinical markers of depression, with a bidirectional relationship. Their changes could precede the increase of suicidal behavior as sleep and appetite are both influenced by mood state and regulated by the serotonergic system. Our hypothesis is that tracking mental health simptoms regularly through self-report could serve as a consistent and non-biased shortcut to assess mood state, its biological underpinnings and could potentially predict suicidal behavior. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03686670
Study type Observational
Source University Hospital, Brest
Contact
Status Completed
Phase
Start date November 1, 2016
Completion date December 1, 2017
View Details
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