Prevention Trial to Achieve Cardiovascular Targets

Completed · Not applicable

Conditions studied: Coronary Artery Disease, Peripheral Arterial Disease, Hyperlipidemia, Hypertension, Diabetes, Prediabetes, Obesity

In brief

The objective of IMPACT (Investigation of Motivational Interviewing and Prevention Consults to Achieve Cardiovascular Targets) is to determine the best management strategy for patients undergoing cardiovascular intervention. IMPACT is a prospective randomized trial that will enroll 400 patients post-cardiovascular intervention. The study will compare different cardiovascular prevention strategies: (1) usual care, (2) cardiovascular prevention consult, and (3) cardiovascular prevention consult with a behavioral intervention program over a 6-month period. The trial hypothesis is that for patients undergoing a cardiovascular intervention, a prevention consult and behavioral intervention is superior to usual care in reducing cardiovascular risk. The primary endpoint will be non-HDL cholesterol. Secondary endpoints include other lipid values, metabolic risk, smoking cessation, physical activity, nutritional status, medication adherence and quality of life. IMPACT is scheduled to begin enrollment in the June of 2012.

Key facts

Study ID

NCT01642355

Run by

NYU Langone Health

People needed

400

Starts

2012-06-01

Expected to finish

2016-05-01

Last updated by the study team

2017-01-02

Who can join

Age: 21 and older, up to 99. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• at least 21 years of age or older
• Subjects scheduled to undergo a percutaneous coronary or peripheral vascular intervention
• Patients must have the ability to understand and the willingness to sign a written informed consent document

You may not qualify if…

• Life expectancy less than 1-year
• Inability to walk

Where it is running

• New York University Langone Medical Center — New York, New York, United States

Full record on ClinicalTrials.gov

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