Clinical Trial

MetSense Pilot and Feasibility

Study acronym: MetSenseP&F
Enrolling by Invitation
View on ClinicalTrials.gov →
Summary
People with serious mental illness have high risk for type 2 diabetes due to multiple risk factors, including the metabolic side effects of psychotropic medications that are used to treat these conditions. Type 2 diabetes is preventable through lifestyle and pharmacological interventions, but many people with serious mental illness do not receive regular screening for type 2 diabetes risk. In many health care settings, clinical pharmacists are increasingly managing patients with serious mental illness and have expertise in monitoring the metabolic side effects of psychotropic medications. This study evaluates the feasibility and acceptability of using a diabetes prediction model that is based on electronic health record data (the MetSense risk flag) to alert clinical pharmacists about patients who are at high diabetes risk, prompting these clinicians to prioritize diabetes risk management services.
Protocol Amendment History 4 amendments
This ClinicalTrials.gov record has been amended 4 times since 2025-11-24; most recent amendment 2026-02-25.
Status change: Not Yet Recruiting → Enrolling by Invitation 2025-12-16
Trial Details
NCT Number NCT07264062
Lead Sponsor Kaiser Permanente
Collaborators: National Institute of Mental Health (NIMH)
Conditions Serious Mental Illness, Type 2 Diabetes
Enrollment 20,000 participants
Start Date 2025-12-01
Primary Completion 2026-12-31 (estimated)
Study Completion 2026-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-02-27