Implementation of New Exercise Protocols in Cardiac Rehabilitation.
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: inspiratory muscle training.
- Who it may be relevant to
- Registry conditions: Heart Diseases, Cardiac Disease, Inspiratory Muscle Training. Basic parameters: 18 years — 80 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
* 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.
Interventions
- Device inspiratory muscle training
inspiratory muscle training for intervention group
Primary outcome measures
- Maximal inspiratory pressure [Time frame: 1 year]
Eligibility criteria
Inclusion criteria
\- 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.
Exclusion criteria
- \- Minor (<18 years old).
- 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.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07161219 · à compléter