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

Physical therapy for patients with an indication for abdominal aortic aneurysm (AAA) repair; a pilot, correlation study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN10008907
Enrollment
100
Registered
2023-09-20
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-10-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients with an indication for elective abdominal aorta aneurysm (AAA) surgery (endovascular and open surgery). Circulatory System

Interventions

Patients included in these studies must fill out a questionnaire, with the assistance of a research nurse, and perform a cardiopulmonary evaluation. Depending on the outcome and training capability, s

Sponsors

University Medical Center Groningen
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

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

Exclusion criteria

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).

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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 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 3. The effect of the program with the Luscii-app using a questionnaire at the first postoperative, outpatient control

Countries

Netherlands

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026