Working with a health system, the investigators will recruit practices to participate in the pilot study, consent and enroll patients with major depressive disorder, and collect the PHQ-9 from those patients at three timepoints (baseline, 6 months post-enrollment, and 12 months post-enrollment). The PHQ-9 will be captured either at an office visit or directly from patients. The investigators will build and implement an open-source SMART on FHIR app to collect key data from the EHR, combine that data with the PHQ-9 results, and present the measurements back to the clinicians. The investigators will then obtain feedback from clinicians on the value and usefulness of the app.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Death from suicide
Timeframe: 12-month intervals
Improvement in Depressive Symptoms: Remission
Timeframe: Baseline
Improvement in Depressive Symptoms: Remission
Timeframe: 6 months post baseline (+/- 60 days)
Improvement in Depressive Symptoms: Remission
Timeframe: 12 months post baseline (+/- 60 days)
Improvement in Depressive Symptoms: Response
Timeframe: Baseline
Improvement in Depressive Symptoms: Response
Timeframe: 6 months post baseline (+/- 60 days)
Improvement in Depressive Symptoms: Response
Timeframe: 12 months post baseline (+/- 60 days)
Worsening in Depressive Symptoms: Recurrence
Timeframe: Baseline
Worsening in Depressive Symptoms: Recurrence
Timeframe: 6 months post baseline (+/- 60 days)
Worsening in Depressive Symptoms: Recurrence
Timeframe: 12 months post baseline (+/- 60 days)
Adverse Events
Timeframe: Baseline
Adverse Events
Timeframe: 6 months post baseline (+/- 60 days)
Adverse Events
Timeframe: 12 months post baseline (+/- 60 days)
Suicide Ideation and Behavior
Timeframe: Baseline
Suicide Ideation and Behavior
Timeframe: 6 months post baseline (+/- 60 days)
Suicide Ideation and Behavior
Timeframe: 12 months post baseline (+/- 60 days)