Clinical trial Recruiting at 2 sites Interventional Ages 18 and up

Care coordination with passive mobile monitoring to help veterans with serious mental illness

Official title: Care Coordination and Passive Mobile Data Monitoring to Engage Veterans and Improve Mental Health Care

Run by VA Office of Research and Development · NCT07549178 · Data updated 2026-11-12

This project tests a care-coordination approach that uses passive mobile data and peer coaching to help veterans with serious mental illness avoid emergency care and stay connected with their care teams.

More Serious Mental Illness trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment400 (estimated)
SponsorVA Office of Research and Development
Federal
Locations2 sites (West Los Angeles, California and 1 other locations)
StatusRecruiting
StartedAugust 10, 2026
Main results expectedOctober 31, 2029
Study endsApril 30, 2030
Registry record updatedAugust 19, 2026
Trial IDNCT07549178 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal participants are veterans with schizophrenia, schizoaffective disorder, or bipolar disorder who receive VA care, have a high CAN score, and own a smartphone.

Probably not a fit

Participants not benefiting may include those unlikely to engage with mobile monitoring or peer coaching or whose care needs fall outside the program’s scope.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This interventional study focuses on veterans with serious mental illness who are at high risk for hospitalization. It tests enhanced care coordination delivered through a mobile intervention that passively monitors mental health indicators and provides support from peer coaches within a VA behavioral health program. The goal is to detect worsening symptoms in real time and reduce the need for acute care services compared with usual care. The study design emphasizes co-design activities with veterans and clinicians to adapt the program for practical implementation in VA settings.

Why it matters

Potential benefit: If successful, the approach could reduce emergency and hospital use and improve coordination of care for veterans with serious mental illness.

How similar studies have gone: Prior studies suggest that mobile monitoring and peer-support approaches can improve engagement and reduce crises, but results vary by population and setting.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* a medical record diagnosis of Serious Mental Illness (SMI)

  * defined as schizophrenia, schizoaffective disorder, or bipolar disorder
* receipt of care at the VA site during the prior 9 months
* a Care Assessment Need (CAN) score over the 75th percentile, indicating high risk for hospitalization or death in the upcoming year
* ownership of a smart phone

Exclusion Criteria:

* none

Where it's running

  • VA Greater Los Angeles Healthcare System, West Los Angeles, CA
    West Los Angeles, California, United States
    Recruiting
  • Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA
    Philadelphia, Pennsylvania, United States
    Recruiting

Study contacts

  • Principal investigator: Alexander Stehle Young, MD MSHS — VA Greater Los Angeles Healthcare System, West Los Angeles, CA
  • Study coordinator: Ronald Calderon, MSW
  • Email: ronald.calderon@va.gov
  • Phone: (310) 478-3711

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.