NCT06856915Completed
Effects of Home-based Respiratory Muscle Training Progamme in Individuals With Ischemic Heart Disease
Effects of Home-based Respiratory Muscle Training by Telerehabilitation on Quality of Life, Cardiopulmonary Function, Physical Status and Psychological Status in Individuals With Ischemic Heart Disease
Source: ClinicalTrials.gov · Last updated 23 Mar 2026
Brief summary (registry, in English)
The main objective of the present study is to verify whether respiratory muscle training programme (IMT+EMT; included both inspriratory and expiratory muscles), applied by telerehabilitation, is an effective intervention (versus placebo and versus inspiratory muscle training in isolation (IMT)) in improving quality of life, cardiopulmonary function and physical and psychological state in people with ischemic heart disease. In addition, the aim is to determine whether respiratory muscle training (IMT or IMT+EMT) is effective in enhancing the results obtained by a conventional cardiac rehabilitation programme on the aforementioned variables.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 104 (actual)
- First submitted
- 20 Jan 2025
- Start date
- 1 May 2025
- Primary completion date
- 6 Feb 2026
- Lead sponsor
- Universidad Complutense de Madrid
- Diseases
- Coronary artery disease
- NCT number
- NCT06856915
What you commit to
- Study type: Interventional
- Participants enrolled: 104
- From 1 May 2025 to the primary completion date, 6 Feb 2026
- 1 site 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.
Prior treatment
- Previous participation in a rehabilitation programme within the last 3 months
Other illness
- Any condition that contraindicate exercise training
Other
- Inability to close the lips to hold the training device's mouthpiece (e.g., facial paralysis)
- Pregnancy
- Inability to adhere to remote monitoring
Who the study is looking for
- Presence of ischemic heart disease
- Age 18 years or older
- Cardiovascular clinical stability
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Departamento de Radiología, Rehabilitación y Fisioterapia, Facultad de Enfermería, Fisioterapia y Podología, Universidad Complutense de Madrid Coordinator of this site? Confirm its status | Madrid | Spain | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.