NCT07161219Not yet recruiting
Implementation of New Exercise Protocols in Cardiac Rehabilitation.
Source: ClinicalTrials.gov · Last updated 23 Sept 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
* Primary Objective: To evaluate the effects of complementary exercise protocols in cardiac rehabilitation (CR), such as inspiratory muscle training (IMT), by assessing inspiratory muscle strength. * Secondary Objectives: To assess functional capacity, quality of life (QoL), and pulmonary function.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 80 (estimated)
- First submitted
- 21 Mar 2025
- Start date
- 1 Dec 2025
- Primary completion date
- 1 Dec 2025
- Lead sponsor
- Cliniques universitaires Saint-Luc- Université Catholique de Louvain
- Diseases
- Heart failure
- NCT number
- NCT07161219
What you commit to
- Study type: Interventional
- Planned participants: 80
- From 1 Dec 2025 to the primary completion date, 1 Dec 2025
- No sites listed in no 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.
Age
- \- Minor (\<18 years old).
Other
- Pregnant woman.
- Patient unable to provide informed consent.
- Patient with cognitive, neurological, or orthopedic limitations.
- Patient with mobility or musculoskeletal difficulties incompatible with physical activity.
- Clinical instability.
Who the study is looking for
- \- Patient meeting the conditions of the permanent life support agreement following hospitalization for a cardiac condition such as: acute myocardial infarction; coronary surgery; therapeutic percutaneous endovascular intervention on the coronary arteries, under medical imaging guidance; therapeutic percutaneous endovascular intervention on the heart, under medical imaging guidance; surgery for congenital or acquired heart malformation; surgery for valvular lesion; heart transplantation; resistant angina (to be specified by detailed history, medical history, and technical examinations, justifying multidisciplinary care); cardiomyopathy with left ventricular dysfunction (to be specified by detailed history, medical history, and technical examinations, justifying multidisciplinary care).
- Patient aged between 18 and 80 years.
- Patient capable of giving informed consent.
- Patient registered for permanent life support at the CuSL.
- Patient capable of understanding instructions in French. - Patient with prior medical consent and clinically stable.
Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.