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Mental Health Symptom Monitoring Utilizing the Cogito Behavioral Analytic Platform

V

VA Eastern Colorado Health Care System

Status

Completed

Conditions

Feasibility
Mental Health Issue
Acceptability of Health Care
Cell Phone Use
Mobile Applications

Treatments

Behavioral: Cogito Companion

Study type

Interventional

Funder types

Other U.S. Federal agency

Identifiers

NCT04150354
16-0109

Details and patient eligibility

About

The primary objective of this project is to test the acceptability and feasibility of a mobile application to facilitate mental health symptom monitoring and follow-up among Veterans. During the course of the study, the research application will be installed on participants' mobile phone. The application on the participants' phone will be recording data about their behavior. Participants will also be asked to complete bi-weekly surveys via the app.

Enrollment

107 patients

Sex

All

Ages

18 to 89 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Veterans between the ages 18-89 years of age at the time of enrollment
  • able to provide signed and dated informed consent
  • has anandroid platform phone and is willing to use phone and personal data plan to participate

Exclusion criteria

  • Participation in conflicting Rocky Mountain MIRECC interventional protocol

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

107 participants in 1 patient group

Participants allocated to Cogito Companion
Experimental group
Description:
Participants will have access the Cogito Companion for a three-month period post-consent. Passive data collection will also occur during this period. As a secure, privacy-compliant mobile app, the Cogito Companion facilitates the non-invasive collection, transfer, integration, analysis, and reporting of objective behavioral indicators.
Treatment:
Behavioral: Cogito Companion

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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