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NCT03269708 Clinical Trial

Improving Cardiac Secondary Prevention

Myocardial Infarction Clinical Trial

Official title:
Improving Cardiac Secondary Prevention Through Personalized Biomarker Knowledge

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT03269708
Other study ID # 109209
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date March 1, 2019
Est. completion date September 2024

Study information
Verified date May 2024
Source Western University, Canada
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether providing individuals with personalized information on cellular aging, including telomere length, will stimulate them to adhere to cardiac prevention strategies and improve exercise capacity.

Description:

Individuals who have sustained a heart attack are at considerable risk for future cardiac events. A cardiac rehabilitation and exercise program can reduce this risk but it remains a challenge to adopt optimum lifestyle changes. We will determine whether providing individuals with information on leukocyte telomere length, will motivate them to improve their exercise performance. We will test whether professionally conveying this information will stimulate an individual to adhere to proven cardiac prevention strategies, looking at the extent to which one's exercise capacity improves over time.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 200
Est. completion date September 2024
Est. primary completion date September 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Individuals who have sustained a myocardial infarction and entered the cardiac rehabilitation program Exclusion Criteria: 1. Individuals with genetic mutations that affect telomere length 2. Individuals who may not have the mental capacity to understanding the ramifications of risk biomarkers

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Education regarding telomere length
Teaching concepts of cellular aging and telomere length

Locations
Country Name City State
Canada London Health Sciences Centre, Western University London Ontario

Sponsors (1)
Lead Sponsor Collaborator
Western University, Canada

Country where clinical trial is conducted

Canada, 

Outcome
Type Measure Description Time frame Safety issue
Primary Exercise capacity based on cardiopulmonary exercise testing Online VO2 maximum after 6-month cardiac rehabilitation program
Secondary Adherence to supervised exercise sessions Proportion of prescribed supervised on-site exercise sessions attended 6 months
Secondary Activity assessment Garmin recording 6 months
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