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Official title Determinants of Cardiorespiratory Fitness and Effects of HIIT in Patients With ANOCA Obstructive Coronary Artery Disease(ANOCA)
ClinicalTrials.gov ID: NCT07182955
What this study is testing
- What it's testing
- The main goal is to understand what causes reduced fitness in ANOCA and whether targeted exercise can help improve it. This study aims to better understand why patients with Angina and No Obstructive Coronary Artery Disease (ANOCA) have poor cardiorespiratory fitness and its effect on quality of life.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 85
You may be able to join if
- Age 18-85
- ANOCA (Anginal symptoms of chest pain or exertional dyspnea suspected to be from myocardial ischemia Invasive or CT coronary angiogram without...
- Able to use the wearable and participate in a remote exercise program
- Able to participate in intermittent high-intensity training.
- Able to perform cardiopulmonary exercise testing (CPET)
You likely can't join if
- Systolic heart failure (LVEF \<50% or NYHA class III symptoms)
- Prior myocardial infarction, coronary revascularization
- Inability to safely undergo cardiopulmonary exercise testing, based on investigator's judgment
- Pregnancy (due to unknown effects on CPET exercise markers)
- Inability to provide informed consent
- Life expectancy \<1 year
See the full eligibility criteria
- Age 18-85
- ANOCA (Anginal symptoms of chest pain or exertional dyspnea suspected to be from myocardial ischemia Invasive or CT coronary angiogram without obstructive epicardial CAD (≥50% left main or ≥70% other epicardial stenosis...
- Able to use the wearable and participate in a remote exercise program
- Able to participate in intermittent high-intensity training.
- Able to perform cardiopulmonary exercise testing (CPET)
- Able to provide Health-related quality of life questionnaire (HRQOL)
- Participants must be able to understand and provide informed consent in English and complete the study questionnaire in English
- Systolic heart failure (LVEF \<50% or NYHA class III symptoms)
- Prior myocardial infarction, coronary revascularization
- Inability to safely undergo cardiopulmonary exercise testing, based on investigator's judgment
- Pregnancy (due to unknown effects on CPET exercise markers)
- Inability to provide informed consent
- Life expectancy \<1 year
- Prisoners
- Cognitively impaired
- Non-English speaking
The study team makes the final eligibility decision.
Where it's taking place
- Charlottesville, Virginia, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 85 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Charlottesville, Virginia, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.