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PRIME Care (PRecision Medicine In MEntal Health Care)

Not Applicable
Completed
Conditions
Major Depression
Interventions
Other: Pharmacogenetic Test
Registration Number
NCT03170362
Lead Sponsor
VA Office of Research and Development
Brief Summary

The focus of this application is on the impact of providing depressed Veterans and their providers with the results of pharmacogenetic (PGx) testing for psychotropic medications. The project focuses on whether and how patients and providers use genetic test results given to them at the time an antidepressant is to be initiated to treat Major Depressive Disorder (MDD) and whether use of the test results improves patient outcomes. MDD is one of the most common conditions associated with military service and combat exposure, increases suicide risk, and worsens the course of common medical conditions, making it a leading cause of functional impairment and mortality. Validation of a PGx test to personalize the treatment of MDD represents an important opportunity to improve the healthcare of Veterans.

Detailed Description

Background: In the last several years, commercial pharmacogenetic (PGx) testing for psychotropic medications has become widespread as a means of implementing "precision medicine", with some insurers electing to cover the cost of testing. These developments have put increasing pressure on the Veterans Health Administration to implement a mental health focused PGxs program, especially for treating depression, but without sufficient scientific study to support the utility of clinical application.

Objectives: The investigators propose a program of research to evaluate the utility of PGx testing in treating Major Depressive Disorder.

Methods: The investigators plan a multi-site RCT (n=2000), patient/provider dyads will be randomly assigned to receive results of the PGx battery right after randomization (i.e. intervention group) or after 6 months of treatment as usual (i.e. delayed results group)The study will test the following hypotheses:

1. Veterans with MDD whose care is guided by the results of the PGx battery (the intervention group) will have a higher rate of remission of depression than the delayed results group. (Primary Hypothesis)

2. Provider/patient dyads in the intervention group will use fewer medications that have potential gene-drug interactions based on commercial PGx test results than dyads in the delayed results group (Primary Hypothesis).

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
1944
Inclusion Criteria
  • PHQ-9 score 10 and a presumptive diagnosis of MDD per PHQ-9 criteria
  • at least one prior treatment exposure for MDD (psychotherapy or antidepressant
  • intent to start treatment of the MDD with an antidepressant, simple dose increases will not be considered inclusionary
  • willingness to provide signed, informed consent to participate in the study
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Exclusion Criteria
  • current serious co-occurring psychiatric illness, i.e.:

    • schizophrenia
    • bipolar disorder
    • psychotic major depression
    • borderline or antisocial personality disorder
    • eating disorder
  • active alcohol or other drug use disorder

  • current use of an antipsychotic medication

  • augmentation therapy, e.g.:

    • use of two or more antidepressants at the time of randomization (trazodone at a dosage < 150 mg/day will not be considered augmentation and thus allowed)
  • patients requiring urgent care or inpatient hospitalization at the time of consent

  • currently incarcerated

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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intervention groupPharmacogenetic TestPharmacogenetic test results will be provided to the provider within 72 hours of randomization in order to facilitate choice in selecting antidepressants.
Primary Outcome Measures
NameTimeMethod
Depression Remission24 weeks post randomization

The investigators will use the Patient Health Questionnaire 9 (PHQ9) as a self assessed marker of depression remission. The scale ranges from 0 to 27 with lower scores indicating less depression severity. Remission was defined as a score of 5 or less at the endpoint. the reported number of participants are those reaching that threshold of symptoms.

Use of Fewer Medications That Have Potential Gene-drug InteractionsOver the first 30 days

The investigators will examine the proportion of antidepressants prescribed in the first 30 days of the trial that have the potential for gene-drug interactions. The chance for a gene-drug interaction was classified as 1. the subject did not have a prescription for an antidepressant during the initial 4 weeks of the trial (No Antidepressant), 2 the subject was prescribed an antidepressant with no known gene-drug interaction (No Gene Interaction), 3 the subject was prescribed an antidepressant with moderate gene-drug interactions (Moderate Interaction). These are also gene-drug interactions that do not have level A concordance. And 4. the subject was prescribed an antidepressant with substantial gene-drug interactions or gene-drug interactions that are considered to have a high level of evidence to support other prescribing.

Secondary Outcome Measures
NameTimeMethod
Depression Response24 weeks

The investigators will use the Patient Health Questionnaire 9 (PHQ9) as a self assessed marker of depression remission. The scale ranges from 0 to 27 with lower scores indicating less depression severity. Response was measured by a 50% reduction in scores from baseline to each time point.

Depression Severity24 Weeks

The investigators will use the Patient Health Questionnaire 9 (PHQ9) as a self-assessed marker of depression remission. The scale ranges from 0 to 27 with lower scores indicating less depression severity. This measure will use the PHQ9 as a continuous measure. The reported outcome is the difference in scores from baseline to 24 weeks.

Trial Locations

Locations (24)

Baltimore VA Medical Center VA Maryland Health Care System, Baltimore, MD

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Baltimore, Maryland, United States

Corporal Michael J. Crescenz VA Medical Center, Philadelphia, PA

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Philadelphia, Pennsylvania, United States

VA Boston Healthcare System Jamaica Plain Campus, Jamaica Plain, MA

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Boston, Massachusetts, United States

Louis Stokes VA Medical Center, Cleveland, OH

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Cleveland, Ohio, United States

VA Puget Sound Health Care System Seattle Division, Seattle, WA

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Seattle, Washington, United States

Miami VA Healthcare System, Miami, FL

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Miami, Florida, United States

Michael E. DeBakey VA Medical Center, Houston, TX

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Houston, Texas, United States

San Francisco VA Medical Center, San Francisco, CA

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San Francisco, California, United States

Cincinnati VA Medical Center, Cincinnati, OH

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Cincinnati, Ohio, United States

Central Arkansas Veterans Healthcare System Eugene J. Towbin Healthcare Center, Little Rock, AR

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North Little Rock, Arkansas, United States

Rocky Mountain Regional VA Medical Center, Aurora, CO

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Aurora, Colorado, United States

VA Palo Alto Health Care System, Palo Alto, CA

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Palo Alto, California, United States

VA Greater Los Angeles Healthcare System, West Los Angeles, CA

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West Los Angeles, California, United States

VA Ann Arbor Healthcare System, Ann Arbor, MI

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Ann Arbor, Michigan, United States

Wilmington VA Medical Center, Wilmington, DE

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Wilmington, Delaware, United States

VA Connecticut Healthcare System West Haven Campus, West Haven, CT

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West Haven, Connecticut, United States

Minneapolis VA Health Care System, Minneapolis, MN

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Minneapolis, Minnesota, United States

New Mexico VA Health Care System, Albuquerque, NM

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Albuquerque, New Mexico, United States

VA Western New York Healthcare System, Buffalo, NY

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Buffalo, New York, United States

Salisbury W.G. (Bill) Hefner VA Medical Center, Salisbury, NC

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Salisbury, North Carolina, United States

VA Pittsburgh Healthcare System University Drive Division, Pittsburgh, PA

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Pittsburgh, Pennsylvania, United States

Ralph H. Johnson VA Medical Center, Charleston, SC

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Charleston, South Carolina, United States

VA Salt Lake City Health Care System, Salt Lake City, UT

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Salt Lake City, Utah, United States

Hunter Holmes McGuire VA Medical Center, Richmond, VA

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Richmond, Virginia, United States

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