About the Study
Currently Recruiting: Participants
Study Drug/Intervention: Evaluating multifaceted strategies to (1) increase LDL-C testing and appropriate management in the inpatient setting for patients hospitalized for myocardial infarction (MI) or coronary revascularization and (2) increase LDL-C testing, appropriate management, and achievement of guideline-based LDL-C goals in the outpatient setting within six months of discharge.
Anticipated Sample Size: 400 patients
Study Anticipated End Date: July 2025
ClinicalTrials.gov ID: NCT06471036
What is Test 2 Treat?
Test 2 Treat is an implementation science study that combines an inpatient, hospital-level intervention and an outpatient, patient-level, randomized intervention to improve LDL-C testing and treatment in six participating health systems. It is a project of the CardioHealth Alliance.
Study Objective
To increase LDL-C testing and appropriate management in the inpatient setting for patients hospitalized for a cardiac event, and to increase LDL-C testing, appropriate management, and achievement of guideline-based LDL-C goals in the outpatient setting within six months of discharge.
Inclusion & Exclusion Criteria
Inclusion Criteria
- Age ≥ 18 years old
- Admitted with Type 1 non-ST-elevation myocardial infarction (NSTEMI) or ST-elevation myocardial infarction (STEMI), and/or percutaneous coronary revascularization.
- LDL-C level during admission ≥ 70 mg/dL.
- Primary care clinician and/or cardiologist within the health system (and with access to the same electronic health records) who will manage the patient in the outpatient setting.
Exclusion Criteria
- Determined to be highly unlikely to survive and/or to continue follow-up in that health system for at least six months (including those on hospice or with significant dementia), as identified by the site investigator.
- Underwent coronary artery bypass grafting (CABG) (patient would therefore be discharged from surgical service).
Patient Population
Patients over 18 who have been admitted to the hospital with a Type 1 NSTEMI or STEMI and/or percutaneous coronary revascularization who are found to have an LDL-C level during admission greater than or equal to 70mg/dL will be approached for participation in Test 2 Treat.
Study Timeline
Duration of Study Participation
Six months
Study Follow-Up
Patients randomized to the intervention arm will receive telephone calls from a "Care Navigator" two to three times during the six months after their event and will be asked to answer some questions about their care.
Study Sites
Louisiana
- Ochsner Health
Minnesota
- Allina Health
North Carolina
- Duke University
Pennsylvania
- University of Pittsburgh Medical Center
Tennessee
- Vanderbilt University Medical Center
Texas
- Baylor, Scott, & White Health
Sponsor/Funding
Amgen, Inc.