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Exercise for people with an enlargement of the body’s main artery

Not Applicable
Conditions
Patients with an indication for elective abdominal aorta aneurysm (AAA) surgery (endovascular and open surgery).
Circulatory System
Registration Number
ISRCTN10008907
Lead Sponsor
niversity Medical Center Groningen
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Ongoing
Sex
All
Target Recruitment
130
Inclusion Criteria

All patients with an indication for elective AAA surgery (endovascular and open surgery).

Exclusion Criteria

1. Patients with an acute indication for surgery (symptomatic or ruptured AAAs)
2. Patients with an indication for priority surgery: saccular aspect
3. Patients with tissue disorders (e.g. Marfan or other).

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in VO2 at the ventilatory anaerobic threshold (VAT) and oxygen uptake at peak exercise (VO2peak) after the 6-week prehabilitation program. The VAT will be measured at inclusion (3-9 weeks in advance of the operation) in a cardiopulmonary exercise test (CPET), and again after 3-9 weeks of training. This CPET will report the VAT in ml/kg/min. The difference between the first measurement and the second measurement will be the primary outcome. The oxygen uptake at peak exercise (VO2peak) will be compared as well.
Secondary Outcome Measures
NameTimeMethod
1. Program feasibility (recruitment rate, adherence, completion rate, drop-out rate, attrition rate, and adverse events) using patient records at the end of the study<br>2. The (preliminary) effect of the program on other cardiopulmonary exercise testing (CPET) values at inclusion (3-9 weeks in advance of the operation) and again after 3-9 weeks of training<br>3. The effect of the program with the Luscii-app using a questionnaire at the first postoperative, outpatient control
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