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The Genomic Medicine at VA Study (GenoVA)

Primary Purpose

Coronary Artery Disease, Atrial Fibrillation, Type 2 Diabetes

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Polygenic risk score (PRS)
Sponsored by
Boston VA Research Institute, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Coronary Artery Disease focused on measuring Polygenic risk score, Coronary artery disease, Atrial fibrillation, Type 2 diabetes, Colorectal cancer, Breast cancer, Prostate cancer

Eligibility Criteria

50 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 50-70 years at enrollment
  • No known diagnosis of the following conditions, initially screened by the International Classification of Disease (ICD) codes or other electronic health record (EHR) data using validated methods and then confirmed with potential patient-participants during recruitment: coronary artery disease, atrial fibrillation, type 2 diabetes, colorectal cancer, breast cancer, prostate cancer

Exclusion Criteria:

  • Patients will be ineligible if they:

    • Have a known diagnosis of at least one of the six diseases of interest
    • Are younger than age 50 or older than age 70
    • Are pregnant
    • Are incarcerated or institutionalized

Sites / Locations

  • VA Boston Healthcare SystemRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Active Comparator

Experimental

Active Comparator

Arm Label

Polygenic risk score (PRS) - high risk stratum

Usual care (UC) - high risk stratum

Polygenic risk score (PRS) - average risk stratum

Usual care (UC) - average risk stratum

Arm Description

Patient-participants in the PRS-high arm and their providers will receive their high-PRS results at baseline, along with educational resources about the results.

Patient-participants in the UC-high arm and their providers will receive their high-PRS results after a 24-month observation period, along with educational resources about the results.

Patient-participants in the PRS-average arm and their providers will receive their average-PRS results at baseline, along with educational resources about the results.

Patient-participants in the UC-average arm and their providers will receive their average-PRS results after a 24-month observation period, along with educational resources about the results..

Outcomes

Primary Outcome Measures

Time-to-new diagnosis of common complex disease
The primary outcome of the study is time-to-diagnosis both of undiagnosed prevalent cases of the 6 target conditions and incident cases during the study period. This composite outcome will only include clinically significant diagnoses, as adjudicated by expert clinical chart review.

Secondary Outcome Measures

Diagnostic testing
Any evidence that the patient-participant underwent additional diagnostic testing for the six target diseases since enrollment: coronary artery disease (stress testing, cardiac CT for coronary artery calcium (CAC), coronary angiography), atrial fibrillation (ECG, heart rhythm monitoring), type 2 diabetes (hemoglobin A1c, blood glucose), colorectal cancer (colonoscopy, sigmoidoscopy, fecal blood testing, CT colonography), breast cancer (mammography, breast MRI, breast ultrasound, breast biopsy), and prostate cancer (PSA testing, prostate biopsy).
Patient activation
Self-reported understanding, competence, and willingness to participate health care decisions and processes assessed on the baseline and end-of-study surveys, using the 13-item short form of the Patient Activation Measure (Hibbard, Health Services Research 2005).
Healthcare costs
A combination of administrative data and microcosting approaches will be used to estimate the costs of the intervention and the subsequent patient-level healthcare costs over the 24 months after enrollment. Estimates of the infrastructure and personnel needed to deliver the intervention will be derived empirically from the study. Healthcare costs will be abstracted from billing and administrative data.
Medication adherence
Self-report of taking medications as prescribed assessed on the baseline and end-of-study surveys, using the 3-item Voils Medication Adherence Survey (Voils, Medical Care, 2012).

Full Information

First Posted
March 31, 2020
Last Updated
September 29, 2022
Sponsor
Boston VA Research Institute, Inc.
Collaborators
VA Boston Healthcare System
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1. Study Identification

Unique Protocol Identification Number
NCT04331535
Brief Title
The Genomic Medicine at VA Study
Acronym
GenoVA
Official Title
Pragmatic Randomized Trial of Polygenic Risk Scoring for Common Diseases in Primary Care
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Recruiting
Study Start Date
July 17, 2020 (Actual)
Primary Completion Date
September 30, 2025 (Anticipated)
Study Completion Date
September 30, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Boston VA Research Institute, Inc.
Collaborators
VA Boston Healthcare System

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This trial will determine the clinical effectiveness of polygenic risk score testing among patients at high genetic risk for at least one of six diseases (coronary artery disease, atrial fibrillation, type 2 diabetes mellitus, colorectal cancer, breast cancer, or prostate cancer), measured by time-to-diagnosis of prevalent or incident disease over 24 months.
Detailed Description
One of the most pressing controversies in genomics today is the clinical utility of polygenic risk scores (PRS). Broadening the scope of genomic risk testing beyond monogenic diseases, PRS combine information from hundreds or even millions of genetic loci, each with a very small effect size on the risk of common complex disease. The result is a continuous quantitative risk factor for susceptibility to conditions such as coronary artery disease (CAD), type 2 diabetes (T2D), and breast cancer. Compared to rarer monogenic disease variants, PRS have greater transformative potential for public health and healthcare in their ability to identify much larger proportions of the population at significantly elevated risk for disease, facilitating evidence-based prevention and management. Moreover, their prediction ability has vastly improved compared to earlier PRS that included only a limited number of genetic variants. However, while the associations between PRS and a wide range of common diseases are well established (clinical validity), the potential impact of this information on patient health outcomes (clinical utility) remains contested and understudied. This study will examine the effectiveness and implementation outcomes from the use of PRS for 6 common diseases that are screened for by PCPs and have established prevention strategies: CAD, AFib, T2D, colorectal cancer, prostate cancer, and breast cancer. This trial has two aims: Aim 1: Conduct a randomized controlled trial (RCT) to determine the clinical effectiveness of PRS among patients at high genetic risk for at least one disease, measured by changes in clinical management (process outcomes) and time to diagnosis of prevalent or incident disease (clinical outcome) over 24 months. Aim 2: Measure high-priority genomic medicine implementation outcomes, including primary care provider (PCP) knowledge and beliefs about PRS, patient activation in healthcare, medication adherence, and costs.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease, Atrial Fibrillation, Type 2 Diabetes, Colorectal Cancer, Breast Cancer, Prostate Cancer
Keywords
Polygenic risk score, Coronary artery disease, Atrial fibrillation, Type 2 diabetes, Colorectal cancer, Breast cancer, Prostate cancer

7. Study Design

Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized clinical trial comparing polygenic risk score (PRS) testing and reporting to delayed reporting
Masking
Outcomes Assessor
Masking Description
Participants are randomized to have them and their primary care providers receive their PRS results at baseline (PRS) or after 24 months (usual care, UC). Randomization is stratified by PRS results: A high-risk stratum consists of all participants with at least one PRS indicating high risk, while the remaining participants comprise the average-risk stratum. Participants who do not receive their results at baseline are blinded to whether they have all average-risk PRS results or any high-risk PRS results. Outcomes assessors and data analysts will be blinded to randomization and PRS results status.
Allocation
Randomized
Enrollment
1076 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Polygenic risk score (PRS) - high risk stratum
Arm Type
Experimental
Arm Description
Patient-participants in the PRS-high arm and their providers will receive their high-PRS results at baseline, along with educational resources about the results.
Arm Title
Usual care (UC) - high risk stratum
Arm Type
Active Comparator
Arm Description
Patient-participants in the UC-high arm and their providers will receive their high-PRS results after a 24-month observation period, along with educational resources about the results.
Arm Title
Polygenic risk score (PRS) - average risk stratum
Arm Type
Experimental
Arm Description
Patient-participants in the PRS-average arm and their providers will receive their average-PRS results at baseline, along with educational resources about the results.
Arm Title
Usual care (UC) - average risk stratum
Arm Type
Active Comparator
Arm Description
Patient-participants in the UC-average arm and their providers will receive their average-PRS results after a 24-month observation period, along with educational resources about the results..
Intervention Type
Diagnostic Test
Intervention Name(s)
Polygenic risk score (PRS)
Intervention Description
Polygenic risk score report from a Clinical Laboratory Improvement Amendment (CLIA)-certified laboratory for coronary artery disease, atrial fibrillation, type 2 diabetes, colorectal cancer, breast cancer (for women only), and prostate cancer (for men only), delivered along with patient- and provider-level educational material.
Primary Outcome Measure Information:
Title
Time-to-new diagnosis of common complex disease
Description
The primary outcome of the study is time-to-diagnosis both of undiagnosed prevalent cases of the 6 target conditions and incident cases during the study period. This composite outcome will only include clinically significant diagnoses, as adjudicated by expert clinical chart review.
Time Frame
24 months after enrollment
Secondary Outcome Measure Information:
Title
Diagnostic testing
Description
Any evidence that the patient-participant underwent additional diagnostic testing for the six target diseases since enrollment: coronary artery disease (stress testing, cardiac CT for coronary artery calcium (CAC), coronary angiography), atrial fibrillation (ECG, heart rhythm monitoring), type 2 diabetes (hemoglobin A1c, blood glucose), colorectal cancer (colonoscopy, sigmoidoscopy, fecal blood testing, CT colonography), breast cancer (mammography, breast MRI, breast ultrasound, breast biopsy), and prostate cancer (PSA testing, prostate biopsy).
Time Frame
24 months after enrollment
Title
Patient activation
Description
Self-reported understanding, competence, and willingness to participate health care decisions and processes assessed on the baseline and end-of-study surveys, using the 13-item short form of the Patient Activation Measure (Hibbard, Health Services Research 2005).
Time Frame
Baseline and 24 months after enrollment
Title
Healthcare costs
Description
A combination of administrative data and microcosting approaches will be used to estimate the costs of the intervention and the subsequent patient-level healthcare costs over the 24 months after enrollment. Estimates of the infrastructure and personnel needed to deliver the intervention will be derived empirically from the study. Healthcare costs will be abstracted from billing and administrative data.
Time Frame
24 months after enrollment
Title
Medication adherence
Description
Self-report of taking medications as prescribed assessed on the baseline and end-of-study surveys, using the 3-item Voils Medication Adherence Survey (Voils, Medical Care, 2012).
Time Frame
Baseline and 24 months after enrollment
Other Pre-specified Outcome Measures:
Title
Provider knowledge and beliefs about PRS
Description
Semi-structured interviews will collect qualitative data on participating providers' understanding of and perceived utility of the PRS risk information.
Time Frame
24 months after enrollment
Title
Blood pressure
Description
The most recent systolic and diastolic blood pressure values recorded in the medical record prior to or on the date of enrollment and prior to or on the date 24 months after enrollment.
Time Frame
Baseline and 24 months after enrollment
Title
Body-mass index (BMI)
Description
The most recent BMI values recorded in the medical record prior to or on the date of enrollment and prior to or on the date 24 months after enrollment.
Time Frame
Baseline and 24 months after enrollment
Title
Aspirin use
Description
Self-reported use of prescription or over-the-counter aspirin will be assessed on the baseline and end-of-study surveys.
Time Frame
Baseline and 24 months after enrollment
Title
Physical activity
Description
Self-reported physical will be assessed on the baseline and end-of-study surveys using the Rapid Assessment of Physical Activity.
Time Frame
Baseline and 24 months after enrollment.
Title
Alcohol intake
Description
Self-reported alcohol will be assessed on the baseline and end-of-study surveys using measures from the Behavioral Risk Factor Surveillance System, recorded as an ordinal 5-item Likert response (from "Never" to "Very often").
Time Frame
Baseline and 24 months after enrollment
Title
Processed meat consumption
Description
Self-reported processed meat intake assessed on the baseline and end-of-study surveys using a food frequency question from National Cancer Institute Eating Habits Questionnaire, recorded as an ordinal 5-item Likert response (from "Never" to "Very often").
Time Frame
Baseline and 24 months after enrollment
Title
Low-density lipoprotein cholesterol (LDL-C)
Description
The most recent LDL-C values recorded in the medical record prior to or on the date of enrollment and prior to or on the date 24 months after enrollment.
Time Frame
Baseline and 24 months after enrollment
Title
Smoking status
Description
Self-reported smoking status will be assessed on the baseline and end-of-study surveys using measures from the Behavioral Risk Factor Surveillance System.
Time Frame
Baseline and 24 months after enrollment
Title
Risk-reducing medication prescriptions
Description
Relevant prescription medication changes during 24-month observation period, including antihypertensives, cholesterol-lowering medications, anticoagulants, antiplatelet medications, 5-alpha reductase inhibitors, selective estrogen receptor modulators, aromatase inhibitors, as abstracted from medical record review.
Time Frame
24 months after enrollment
Title
Health status and quality of life
Description
As determined by data collected from the baseline survey (VR-12)
Time Frame
Baseline and 24 months after enrollment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 50-70 years at enrollment No known diagnosis of the following conditions, initially screened by the International Classification of Disease (ICD) codes or other electronic health record (EHR) data using validated methods and then confirmed with potential patient-participants during recruitment: coronary artery disease, atrial fibrillation, type 2 diabetes, colorectal cancer, breast cancer, prostate cancer Exclusion Criteria: Patients will be ineligible if they: Have a known diagnosis of at least one of the six diseases of interest Are younger than age 50 or older than age 70 Are pregnant Are incarcerated or institutionalized
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jason L. Vassy, MD, MPH, SM
Phone
857-364-2561
Email
jvassy@partners.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jason L. Vassy, MD, MPH, SM
Organizational Affiliation
Harvard Medical School (HMS and HSDM)
Official's Role
Principal Investigator
Facility Information:
Facility Name
VA Boston Healthcare System
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02130-4817
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jason L. Vassy, MD, MPH, SM
Phone
857-364-2561
Email
jvassy@partners.org

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
We will share de-identified individual-level trial data through a data repository housed on a secure VA server and accessible only to outside investigators with Institutional Review Board (IRB).
IPD Sharing Time Frame
Upon publication of primary results
IPD Sharing Access Criteria
Access will be contingent on IRB approval
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Links:
URL
https://knowledge.amia.org/65881-amiab-1.4254737/t004-1.4257399?qr=1
Description
This link references a poster presentation at the annual American Medical Informatics Association (AMIA) in 2017 by authors Majahalme N, Miller SJ, Zimolzak AJ, and Vassy JL.
URL
https://www.va.gov/HEALTHEQUITY/docs/National_Veterans_Health_Equity_Report_FY2013_FINAL_508_Comp.pdf
Description
This link references the National Veterans Health Equity report for FY2013, published by the VA Office of Health Equity.
URL
https://seer.cancer.gov/data-software/documentation/seerstat/nov2017/
Description
This link references the Surveillance, Epidemiology, and End Results (SEER) database from November 2017, published by the NIH.
URL
https://www.cdc.gov/diabetes/pdfs/data/statistics/national-diabetes-statistics-report.pdf
Description
This link references the National Diabetes Statistics Report from 2017, published by the Centers for Disease Control and Prevention (CDC).
URL
https://catalog.loc.gov/vwebv/search?searchCode=LCCN&searchArg=2007002042&searchType=1&permalink=y
Description
This link references a book entitled "Systematic Methods for Collecting and Analyzing Multidisciplinary Team Based Qualitative Data," authored by Carey JW and Gelaude D.
URL
https://methods.sagepub.com/book/applied-thematic-analysis
Description
This link references a book entitled "Applied Thematic Analysis," authored by Guest GS, MacQueen KM, and Namey EE.

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The Genomic Medicine at VA Study

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