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Mobile Sensing and Support for Depression

NCT02776839 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 126

Last updated 2017-06-02

No results posted yet for this study

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.

Conditions

Interventions

DEVICE

Mobile sensing

Sponsors & Collaborators

  • Switzerland: ETH

    collaborator UNKNOWN

  • Switzerland: Makora

    collaborator UNKNOWN

  • University of Zurich

    lead OTHER

Principal Investigators

  • S Weidt, MD · University of Zurich

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-03-31
Primary Completion
2015-12-31
Completion
2015-12-31

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02776839 on ClinicalTrials.gov