NCT07392021Active, not recruiting
Effects of a Recovery-Promoting Program in Patients Undergoing CABG Surgery
The Effects of a Recovery-Promoting Program on Self-Efficacy, Quality of Recovery, and Clinical Outcomes in Patients Undergoing Coronary Artery Bypass Graft Surgery
Source: ClinicalTrials.gov · Last updated 6 Feb 2026
Brief summary (registry, in English)
Patients undergoing coronary artery bypass graft (CABG) surgery often experience physical limitations, psychological stress, and challenges during recovery after hospital discharge. Inadequate preparation and limited follow-up support may affect patients' confidence in self-care and overall recovery. The purpose of this study is to evaluate the effects of a recovery-promoting program on self-efficacy, quality of recovery, and clinical outcomes in patients undergoing CABG surgery. Participants will receive standard postoperative care. In addition, participants in the intervention group will receive a recovery-promoting program provided by nurses, which includes structured education, guidance on postoperative activity and symptom management, and follow-up support after discharge. The study will assess changes in self-efficacy, quality of recovery, and selected clinical outcomes to compare recovery between participants who receive the recovery-promoting program and those who receive standard care.
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 60 (actual)
- First submitted
- 21 Jan 2026
- Start date
- 22 Aug 2025
- Primary completion date
- 31 Jul 2026
- Lead sponsor
- Mahidol University
- Diseases
- Coronary artery disease
- NCT number
- NCT07392021
What you commit to
- Study type: Interventional
- Participants enrolled: 60
- From 22 Aug 2025 to the primary completion date, 31 Jul 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
- Severe or acute comorbidities within 24 hours prior to surgery (e.g., chronic obstructive pulmonary disease, renal failure, acute myocardial infarction, severe arrhythmia)
- Disability or limited ambulation or mobility assessed prior to hospital discharge
Other illness
- Severe postoperative complications or unstable vital signs (e.g., major bleeding, significant arrhythmia, embolism, need for dialysis, extracorporeal membrane oxygenation)
- Failure of extubation within 3 days after surgery or requirement for reoperation
Who the study is looking for
- Thai patients undergoing elective first-time on-pump coronary artery bypass graft (CABG) surgery alone or combined with valve surgery
- If age \>60 years, participants must pass cognitive screening using the 6-Item Cognitive Impairment Test (6-CIT)
- New York Heart Association (NYHA) functional class I-III
- Left ventricular ejection fraction (LVEF) \>30%
- Independent in activities of daily living and able to perform the 6-minute walk test (6MWT)
Age in the registry: 20 years to - · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Rajavithi Hospital, Ministry of Public Health, Thailand Coordinator of this site? Confirm its status | Bangkok | Thailand | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.