RECRUITING

Genetic Risk Stratification for Primary Prevention of CAD in Men and Pre & Post-menopausal Women

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

The investigators propose to genotype males and females at age 40 years and older, who are asymptomatic and without known heart disease (N=2000). DNA from a blood sample will be genotyped for millions of genetic risk variants for CAD by Baylor College of Medicine Human Genome Sequencing Center Clinical Laboratory (HGSC-CL) in a CLIA-approved laboratory. The overall objective after 2 years is to determine if genetic screening for risk of CAD in asymptomatic men and women has the discriminatory power to detect those at highest risk who would potentially benefit most from appropriate primary prevention. It will also determine whether the GRS is appropriate for different ethnic and race groups such as Hispanics, African Americans and Whites, and to what extent those individuals knowing that they are at higher risk, are more likely to seek further advice on management of the risks (either through changes in lifestyle or therapy).

Official Title

Genetic Risk Stratification for Primary Prevention of CAD in Men and Pre & Post-menopausal Women

Quick Facts

Study Start:2021-08-23
Study Completion:2024-06-15
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05169840

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:40 Years to 60 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Yes
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Males 40 to 60 years of age
  2. * Females 40 to 60 years of age
  3. * No known cardiovascular disease
  4. * Willing and able to sign consent
  1. * Prisoners
  2. * Prior percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG)
  3. * Known ischemia on non-invasive testing
  4. * Ischemic cerebrovascular event
  5. * Peripheral arterial disease

Contacts and Locations

Study Contact

Jennine C Zumbuhl, RN, MSHA
CONTACT
480-728-3674
jennine.zumbuhl@dignityhealth.org
Lori Wood, RN
CONTACT
lori.wood@dignityhealth.org

Principal Investigator

Robert Roberts, MD
PRINCIPAL_INVESTIGATOR
Dignity Health

Study Locations (Sites)

Chandler Regional Medical Center
Chandler, Arizona, 85224
United States
Mercy Gilbert Medical Center
Gilbert, Arizona, 85297
United States
St Joseph's Hospital and Medical Center
Phoenix, Arizona, 85013
United States

Collaborators and Investigators

Sponsor: St. Joseph's Hospital and Medical Center, Phoenix

  • Robert Roberts, MD, PRINCIPAL_INVESTIGATOR, Dignity Health

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2021-08-23
Study Completion Date2024-06-15

Study Record Updates

Study Start Date2021-08-23
Study Completion Date2024-06-15

Terms related to this study

Keywords Provided by Researchers

  • Genetic Risk Score
  • Coronary Artery Disease

Additional Relevant MeSH Terms

  • Coronary Artery Disease
  • Genetic Predisposition to Disease