Percutaneous coronary angioplasty compared with exercise training in patients with stable coronary artery disease: a randomized trial.
Rainer Hambrecht, Claudia Walther, Sven Möbius-Winkler...
https://pubmed.ncbi.nlm.nih.gov/15007010/Actively Recruiting
Led by University of Virginia · Updated on 2025-09-19
25
Participants Needed
1
Research Sites
2 weeks
Total Duration
Researchers are investigating the causes of reduced fitness in patients with Angina and No Obstructive Coronary Artery Disease ANOCA and whether a targeted high-intensity interval training HIIT exercise program can improve their heart function, fitness, and quality of life. The study aims to better understand the link between poor cardiorespiratory fitness and quality of life in these patients by using cardiopulmonary exercise testing CPET to identify exercise limitations and phenotypes. Participants will undergo a 4-week remote HIIT exercise program involving three non-consecutive days per week. The program begins with one supervised treadmill session, followed by remote sessions monitored with Polar heart rate devices and an app. Exercise sessions progressively increase from one-minute intervals to four 4-minute sessions. Participants will wear a wrist-based Polar device daily and a chest strap during exercise to monitor heart rate and adherence. During the study, participants will have baseline and post-exercise CPET assessments to measure peak oxygen consumption and exercise fitness. Questionnaires will assess angina symptoms, cardiac anxiety, functional status, and quality of life. Researchers will track adherence to exercise and evaluate changes in fitness and quality of life after the HIIT program. The study duration for each participant is 4 weeks of intervention with assessments before and after training.
CONDITIONS
Determinants of Cardiorespiratory Fitness and Effects of HIIT in Patients With ANOCA Obstructive Coronary Artery Disease(ANOCA)
R
Rahel Askari
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University of Virginia
Lead Sponsor
This table compares participation in this trial with other options available for this condition. The information is drawn from published research and the trial’s study details and is provided for educational purposes only.
| Factors | HIIT intervention (trial) | Current guideline‑recommended care (context) |
|---|---|---|
| What it is | Remote high‑intensity interval exercise training (three sessions per week for 4 weeks) provided to patients with ANOCA | Guideline‑recommended management involves coronary function testing to define ANOCA endotypes and personalized medical therapy |
| Role in trial | Investigational intervention delivered to all participants in a single‑group design | Not part of this study; represents external current standard practice |
| Primary use | To improve cardiorespiratory fitness (VO2 max) and quality of life in ANOCA patients | To diagnose underlying ANOCA mechanisms and guide targeted symptom‑relieving treatments |
| How it is given or performed | Remote sessions of high‑intensity interval training three times weekly over four weeks | Patients undergo coronary function testing followed by tailored pharmacologic or device‑directed therapy based on mechanism |
| Evidence status | Effectiveness in ANOCA is investigational; previous exercise studies in related populations show benefit in fitness and symptoms | Supported by ESC‑recommended mechanism‑based therapy guided by diagnostic testing |
| Important risks | Risks typical of high‑intensity exercise in ischemic patients, such as cardiac strain or arrhythmia | Invasive coronary function testing carries procedural risks such as vascular injury or contrast reactions |
| Important limitations | Single‑group design without control arm limits comparative inference; small sample size | Implementation depends on availability of specialized testing centers and may not be widespread |
Disclaimer: This comparison is created with the help of artificial intelligence(AI) and may contain errors or missing information. It is not medical advice and does not mean one option is better or safer than another. Clinical trials are still being studied, and joining a trial is your choice. Please consult your healthcare professional before making any decisions.
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 1 week
Participants undergo baseline cardiopulmonary exercise testing (CPET) and complete health-related quality of life questionnaires before starting the exercise program.
1 baseline visit (in-person)
Duration - 4 weeks
Participants engage in a remote 4-week high-intensity interval exercise training program on three non-consecutive days per week, starting with one supervised treadmill session and followed by remote sessions using a Polar heart rate monitor.
1 supervised exercise session and remote exercise sessions three days per week
Duration - Within 1 week after treatment
Participants undergo repeat cardiopulmonary exercise testing and complete health-related quality of life questionnaires to assess changes after the exercise program.
1 follow-up visit (in-person)
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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Rainer Hambrecht, Claudia Walther, Sven Möbius-Winkler...
https://pubmed.ncbi.nlm.nih.gov/15007010/Siddhartha S Angadi, Catherine L Jarrett, Moustafa Sherif...
https://pubmed.ncbi.nlm.nih.gov/28772048/University of Virginia
Lead Sponsor