NCT07243444Completed
Home-Based Versus Center-Based Cardiac Rehabilitation After CABG Surgery
Efficacy of Home-Based Telerehabilitation Versus Center-Based Cardiac Rehabilitation on Cardiopulmonary Function and Exercise Capacity in Patients After Coronary Artery Bypass Grafting: A Randomized Controlled Trial
Source: ClinicalTrials.gov · Last updated 21 Nov 2025
Brief summary (registry, in English)
This randomized controlled trial was designed to compare the efficacy of a 12-week home-based telerehabilitation (HBTCR) program against traditional center-based cardiac rehabilitation (CBCR) and usual care in patients who have undergone coronary artery bypass grafting (CABG). The primary goal was to assess changes in cardiopulmonary function, measured by peak oxygen consumption (VO₂ peak), and exercise capacity, measured by the 6-minute walk test (6MWT), to determine if HBTCR is a viable alternative to CBCR.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 110 (actual)
- First submitted
- 14 Nov 2025
- Start date
- 1 Sept 2024
- Primary completion date
- 1 Sept 2025
- Lead sponsor
- The First Hospital of Hebei Medical University
- Diseases
- Coronary artery disease
- NCT number
- NCT07243444
What you commit to
- Study type: Interventional
- Participants enrolled: 110
- From 1 Sept 2024 to the primary completion date, 1 Sept 2025
- 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.
Other illness
- Acute decompensated heart failure.
- Severe physical comorbidities (e.g., fractures, severe hearing impairment) that would preclude participation in an exercise program.
- Recent stroke or pulmonary embolism.
- Unstable angina.
Other
- Significant hepatic or renal dysfunction.
Who the study is looking for
- Patients aged 30 to 75 years.
- Had undergone Coronary Artery Bypass Grafting (CABG) 4 to 8 weeks prior.
- In a stable clinical condition.
- Able to provide written informed consent.
- No cognitive impairments.
Age in the registry: 30 years to 75 years · 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 |
|---|---|---|---|
| The First Hospital of Hebei Medical University Coordinator of this site? Confirm its status | Shijiazhuang | China | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.