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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00626379
Other study ID # 1379
Secondary ID R01HL081141-04
Status Completed
Phase
First received
Last updated
Start date November 2007
Est. completion date December 2010

Study information

Verified date May 2023
Source Northwestern University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Heart disease is the leading cause of death in the United States and is responsible for 30% of all deaths in the United States. This study will examine how risk factors for heart disease in young and middle aged people affect people's health as they grow older.


Description:

Heart disease, including coronary heart disease (CHD) and cardiovascular disease (CVD), is a serious health problem in the United States. It is the leading cause of death in this country, and each year almost 700,000 people die from the disease. Risk factors for heart disease include high blood pressure, high cholesterol levels, tobacco use, diabetes, and history of a prior heart attack. It has been shown that young and middle aged adults with few risk factors experience a lower incidence of heart disease, lower Medicare costs, and longer lives than those with more risk factors. However, it is not known how having a low risk for heart disease at a young age affects health-related outcomes in older age. It may be possible that a low risk for developing heart disease in younger years results in healthier aging than does a higher risk. This study will examine former participants of the Chicago Heart Association (CHA) study who are now 65 to 84 years old. The purpose of this study is to determine how risk factors for heart disease in young adulthood and middle age are related to healthy aging. This study will enroll 1500 people who participated in the CHA study from 1967 to 1973 and who are still living in the Greater Chicagoland area. Six hundred former participants who had a low risk of developing heart disease and 900 former participants who had a high risk of developing heart disease will be enrolled. Participants will attend one study visit that will include medical history interviews and questionnaires, a physical examination, blood pressure measurements, blood and urine collection, and an electrocardiogram (ECG) to measure the electrical activity of the heart. Blood samples will be collected and stored for future genetic testing. Participants will undergo physical functioning performance tests on balance, leg strength and coordination, grip strength, and endurance. They will also undergo a computed tomography chest scan to measure the amount of calcium in the arteries of the heart and ultrasound scans of the arteries in the neck to measure artery size and function.


Recruitment information / eligibility

Status Completed
Enrollment 1395
Est. completion date December 2010
Est. primary completion date August 2010
Accepts healthy volunteers No
Gender All
Age group 65 Years to 84 Years
Eligibility Inclusion Criteria: - Participated in the CHA study - Lives in the Greater Chicagoland area Exclusion Criteria: - Severely ill, disabled, or cognitively impaired

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Preventive Medicine Research Clinic Chicago Illinois

Sponsors (2)

Lead Sponsor Collaborator
Northwestern University National Heart, Lung, and Blood Institute (NHLBI)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Subclinical atherosclerosis, CVD-related markers of inflammation, and levels of physical performance Measured during participant's one (baseline) study visit
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