Revalidatiebegeleiding van de patiënt voor en na een hartoperatie ter vermindering van complicaties en verbetering van de kwaliteit van het leven (Heart-ROCQ) - een haalbaarheid pilot studie
- Conditions
- Pre- en postoperative rehabilitationPeri-operative complicationsQuality of lifecardiovascular surgery
- Registration Number
- NL-OMON21761
- Lead Sponsor
- niversity Medical Center Groningen
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Age > 18 years -Accepted for cardiovascular surgery under general anesthesia -Patients (age > 18 years) admitted for coronary bypass surgery, valve surgery or aortic surgery (or combined) -Bed available in the rehabilitation center during the post-operative clinical phase
Exclusion Criteria
-Co-morbidities that prevent participation in one program elements (e.g. disorders to the nervous or musculoskeletal system that limits exercise capacity, severe COPD (GOLD class 3-4), non-coping behaviour/ addiction/ serious psychological illness) or when it is undesirable to exercise -Unable to understand or read Dutch instructions -Unable to sign informed consent before surgery -MRSA-positive -Pregnancy, childbearing potential
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method This study will mainly evaluate post-operative complications (infections, stroke, and heart rhythm problems), duration at the intensive care unit, hospital stay and mortality.
- Secondary Outcome Measures
Name Time Method Secondary, psychophysical parameters (e.g. delirium, post-operative cognitive decline, disability free survival, quality of life, physical fitness, labor participation, and life style) will be evaluated.