NCT07105943Recruiting
Manipulating Exercise Intensity and Affective Responses for Cardiac Rehabilitation Program Acute Coronary Syndrome Patients
Manipulating Exercise Intensity and Affective Responses on a Cardiac Rehabiliattion Program for Patients With Acute Coronary Syndrome: Protocol for a Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 4 May 2026
Brief summary (registry, in English)
The goal of this clinical trial is to learn if pleasure-oriented exercise intensity manipulation increases physical activity (PA) behavior in patients who have suffered acute coronary syndrome during a cardiac rehabilitation program. The main question it aims to answer is: • the manipulation of exercise intensity performed to produce more pleasure and arousal will impact the PA behavior? Researchers will compare the PA levels and affective responses to see if the manipulation of exercise intensity guided to pleasure and arousal works to increase PA behavior compared to the control group who will follow a conventional exercise program. Participants will do: * sixteen individualized hospital exercise sessions (two per week) and complementary physical activity program integrated into their daily life * be evaluated before and at the end of the exercise sessions and after 3 months
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 52 (estimated)
- First submitted
- 17 Jul 2025
- Start date
- 1 Mar 2026
- Primary completion date
- 31 Dec 2027
- Lead sponsor
- Instituto Politécnico de Leiria
- Diseases
- Coronary artery disease
- NCT number
- NCT07105943
What you commit to
- Study type: Interventional
- Planned participants: 52
- From 1 Mar 2026 to the primary completion date, 31 Dec 2027
- 2 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Criteria the registry did not label
- Selection criteria include:
- patients older than 18 years
- diagnosis of ACS within the past 12 months who have not previously participated in a CR program
- patients classified as low-risk (Class B) according to the American Heart Association: (a) New York Heart Association (NYHA) class I or II, (b) exercise capacity greater than 6 METs, (c) no evidence of heart failure, (d) no signs of myocardial ischemia or angina at rest or during exercise testing at or below 6 METs, (e) appropriate systolic blood pressure response during exercise, and (f) absence of sustained or non-sustained ventricular tachycardia at rest or during exercise.
- Standard exclusion criteria include:
- left ventricular ejection fraction (LVEF) \< 40% at rest
- uncontrolled arrythmias (e.g., complex ventricular arrhythmias, atrial fibrillation or flutter with rapid ventricular response, second-degree atrioventricular block Mobitz type II, or third-degree atrioventricular block)
- presence of an implantable cardiac device
- symptomatic peripheral arterial disease
- comorbidities that may interfere with the ability to perform the exercise program safely.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Unidade Local de Saúde da Região de Leiria Coordinator of this site? Confirm its status | Leiria | Portugal | Not yet recruiting |
| Hospital de Leiria Coordinator of this site? Confirm its status | Leiria | Portugal | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.