The AAA Get Fit Trial: A Pilot Randomised Controlled Trial of Community Based Exercise to Improve Fitness and Reduce Morbidity and Mortality of Patients With Abdominal Aortic Aneurysms
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Aortic Aneurysm, Abdominal
- Sponsor
- University of Manchester
- Enrollment
- 58
- Primary Endpoint
- Peak VO2 as measured by CPET
- Last Updated
- 7 years ago
Overview
Brief Summary
Rupture of abdominal aortic aneurysms(AAA) causes 12,000 deaths/year in the UK.1 Elective repair to prevent this carries a perioperative mortality of 4.5% for open surgery and 1% for endovascular repair. This risk is associated with poor cardiorespiratory fitness which can be measured using Cardiopulmonary Exercise Testing(CPET) with the CPET variables, peak oxygen uptake(peakVO2)<15ml/kg/min and anaerobic threshold(AT)<10.2ml/kg/min identifying patients at increased risk of early death after AAA repair.3 These variables can therefore be used as surrogate markers for cardiovascular fitness and risk of mortality and morbidity in AAA surgery; optimising these markers should improve fitness and decrease this risk. The optimal duration and type of exercise training for improving peak VO2 and AT in AAA patients is not known. AAA patients are unique as they are motivated to reduce the risk of impending surgery but are afforded the time to improve their fitness as repair may not be needed for months or even years.
The investigators propose a pilot randomised controlled trial to explore the effectiveness of a 20-week community (either home or gym-based) exercise programme to achieve sustained improvements in peak VO2 and AT, as measured by CPET, in AAA patients. Changes in QoL, habitual activity levels and cardiovascular risk will also be assessed. The results will inform a definitive multicentre clinical trial on exercise to improve outcomes in elderly patients with cardiovascular disease and AAA.
Investigators
Charles McCollum
Professor
University of Manchester
Eligibility Criteria
Inclusion Criteria
- •Men with an AAA ≥ 3.0 and \< 5.0 cm and women with a AAA ≥ 3.0 and \< 4.5 cm
- •Aged 60 - 85 years inclusive
- •Willing and able to engage in gym- and/or home-based exercise training and undertake CPET
Exclusion Criteria
- •Unable or unwilling to undertake CPET or exercise training Patients unwilling will not be able to give informed consent and those who are unable would not be able to be randomised to the intervention study group nor undergo satisfactory testing to obtain our outcome measures.
- •High levels of habitual physical activity (those scoring "high" on the PASE questionnaire) These patients already have a high level of physical activity and therefore it may not be possible to improve their fitness any further which is the primary objective of the study.
- •Exclusion criteria 3-10 are all based on medical conditions which would mean either exercise training may be unsafe, they would require further investigation and treatment of that medical condition or are likely to need upcoming intervention for their medical condition which would take priority over any participation in a research study. If any medical conditions are discovered during the study, these patients will be withdrawn from the study and referred to the necessary health professional.
- •Severe liver disease (INR \> 2, serum albumin \< 3.0g/dL, bilirubin \> 50µmol/L)
- •Unstable angina, angina of \< 2 month's duration, occurring more than twice daily, angina that is increasing in frequency or precipitated by less exertion, angina at rest
- •Uncontrolled atrial fibrillation (AF) or other arrhythmia: untreated paroxysmal AF
- •Moderate or severe aortic valve stenosis (peak systolic pressure gradient \>40mmHg or with an aortic valve area \< 1cm2)
- •Class II/III/IV heart failure and/or left ventricular ejection fraction \< 25%
- •Pericarditis or myocarditis within last six months
- •Patients with \> 2mm ST depression on exercise ECG will not be eligible to take part and will be referred to a cardiologist for further assessment.
Outcomes
Primary Outcomes
Peak VO2 as measured by CPET
Time Frame: at 20 weeks
Secondary Outcomes
- Early changes in outcome measures(at 10 weeks)
- Biomarkers of Cardiovascular disease risk(at 20 weeks)
- Other risk factors of Cardiovascular disease risk(at 20 weeks)
- Subjective measure of habitual activity levels (PASE questionnaire)(at 20 weeks)
- Sustainability of changes in outcome measures(at 30 weeks)
- Anaerobic Threshold as measured by CPET(at 20 weeks)
- Objective measure of habitual activity levels (via Accelerometry)(at 20 weeks)
- Health-related quality of life(at 20 weeks)