Implementation of New Exercise Protocols in Cardiac Rehabilitation.
NCT ID: NCT07161219
Last Updated: 2025-09-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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NOT_YET_RECRUITING
NA
80 participants
INTERVENTIONAL
2025-12-01
2029-12-31
Brief Summary
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* Secondary Objectives: To assess functional capacity, quality of life (QoL), and pulmonary function.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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control group
No interventions assigned to this group
intervention group
inspiratory muscle training
inspiratory muscle training for intervention group
Interventions
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inspiratory muscle training
inspiratory muscle training for intervention group
Eligibility Criteria
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Inclusion Criteria
* 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
* 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.
18 Years
80 Years
ALL
No
Sponsors
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Cliniques universitaires Saint-Luc- Université Catholique de Louvain
OTHER
Responsible Party
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Dayez Martin
Principal investigator
Central Contacts
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Other Identifiers
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à compléter
Identifier Type: -
Identifier Source: org_study_id
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