Clinical Trials Directory

Trials / Completed

CompletedNCT03686670

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

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

Status
Completed
Phase
Study type
Observational
Enrollment
30 (actual)
Sponsor
University Hospital, Brest · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Timeline

Start date
2016-11-01
Primary completion
2017-12-01
Completion
2017-12-01
First posted
2018-09-27
Last updated
2019-05-31

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT03686670. Inclusion in this directory is not an endorsement.