NCT07006441Completed
Cardiac Rehabilitation in Coronary Artery Bypass Graft Surgery
The Effects of Preoperative and Postoperative Cardiac Rehabilitation in Patients Undergoing Coronary Artery Bypass Graft Surgery
Source: ClinicalTrials.gov · Last updated 27 Aug 2025
Brief summary (registry, in English)
This randomized controlled trial investigates the comparative effects of a combined preoperative and postoperative cardiac rehabilitation program versus a postoperative-only program on functional capacity, pulmonary function, peripheral muscle strength, pain, kinesiophobia, and quality of life in patients undergoing coronary artery bypass graft (CABG) surgery. The study aims to determine whether initiating rehabilitation prior to surgery improves short-term postoperative outcomes.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 30 (actual)
- First submitted
- 28 May 2025
- Start date
- Aug 2024
- Primary completion date
- Aug 2025
- Lead sponsor
- Atlas University
- Diseases
- Coronary artery disease
- NCT number
- NCT07006441
What you commit to
- Study type: Interventional
- Participants enrolled: 30
- From Aug 2024 to the primary completion date, Aug 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
- Having an active or suspected infection
- History of thrombophlebitis or pulmonary embolism within the last 3 months
- Having an orthopaedic, neurological or cardiovascular disease that may affect the assessments
Other
- Presence of an active tumour
Who the study is looking for
- Having undergone coronary artery bypass graft surgery
- Ejection Fraction (EF) \> 40%
- Being between the ages of 18-65
- Being able to speak, read and understand in their own language
- Volunteering to participate in the study
Age in the registry: 18 years to 65 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 |
|---|---|---|---|
| Istanbul Atlas University Coordinator of this site? Confirm its status | Istanbul | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.