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HIIT Programs for Cardiac Rehabilitation
N/A
Recruiting
Led By Amanda Bonikowske, PhD
Research Sponsored by Mayo Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Has a qualifying indication for center-based cardiac rehabilitation that is non-surgical (i.e., Acute coronary syndrome, myocardial infarction, percutaneous coronary intervention, and stable angina)
Adult 18 years and older
Timeline
Screening 3 weeks
Treatment Varies
Follow Up weekly, over 12 weeks
Awards & highlights
Study Summary
This trial will compare the effects of two different HIIT programs on fitness, heart function, and muscle oxygen uptake.
Who is the study for?
This trial is for adults over 18 who speak English and can consent to participate. It's specifically for those with certain heart conditions like acute coronary syndrome or stable angina, who are recommended non-surgical cardiac rehab. People post-heart surgery, with heart devices, or unable to do structured exercise aren't eligible.Check my eligibility
What is being tested?
The study compares two types of high-intensity interval training (HIIT) in cardiac rehab: Constant HIIT (CON-HIIT) and Progressive HIIT (PRO-HIIT). The goal is to see which one better improves fitness levels, heart function, and muscle oxygen uptake.See study design
What are the potential side effects?
While the trial itself doesn't involve medication that could cause side effects, high-intensity exercise may lead to muscle soreness, fatigue, shortness of breath during activity or increased risk of injury if not properly monitored.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I need heart rehab for a condition that didn't require surgery.
Select...
I am 18 years old or older.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ weekly, over 12 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~weekly, over 12 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in cardiorepiratory fitness
Secondary outcome measures
Change in blood lipids
Change in blood pressure
Change in body composition
+6 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Progressive interval-training groupExperimental Treatment1 Intervention
Subjects will complete an interval-training program during which the number of intervals and the duration of each interval are changed across the 12-week cardiac rehabilitation program.
Group II: Standard-care interval-training groupActive Control1 Intervention
Subjects will complete a standard interval-training program that remains constant for the entire 12 weeks of cardiac rehabilitation.
Find a Location
Who is running the clinical trial?
Mayo ClinicLead Sponsor
3,213 Previous Clinical Trials
3,766,981 Total Patients Enrolled
1 Trials studying Cardiac Rehabilitation
128 Patients Enrolled for Cardiac Rehabilitation
Amanda Bonikowske, PhDPrincipal InvestigatorMayo Clinic
1 Previous Clinical Trials
Amanda R Bonikowske, PhDPrincipal InvestigatorMayo Clinic
1 Previous Clinical Trials
60 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I was referred to cardiac rehab after heart surgery or because I have a ventricular assist device.I need heart rehab for a condition that didn't require surgery.I am 18 years old or older.
Research Study Groups:
This trial has the following groups:- Group 1: Progressive interval-training group
- Group 2: Standard-care interval-training group
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
How many participants are being considered for this research endeavor?
"Affirmative. Data from clinicaltrials.gov conveys that this medical trial, first posted on June 23rd 2021, is actively looking for individuals to participate in the study. 30 subjects are expected to be recruited from a single site."
Answered by AI
Can individuals still join this research endeavor?
"Affirmative. According to the clinicaltrial.gov database, this medical research is presently recruiting volunteers; it was originally posted on June 23rd 2021 and last modified at the end of July 2022. The project requires 30 individuals from a single site."
Answered by AI
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