The AAA Get Fit Trial: A Pilot Randomised Controlled Trial of Community Based Exercise in Patients With Abdominal Aortic Aneurysms

NCT02997618 | Unknown

• 1 other identifier: 162347
• Study Type: interventional
• Target: 58
• Locations: 0 countries
• Sites: N/A

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.

Conditions

Aortic Aneurysm, Abdominal

Outcome Measures

Primary Outcomes (1)

• Peak VO2 as measured by CPET

  at 20 weeks

Secondary Outcomes (8)

• Anaerobic Threshold as measured by CPET

  at 20 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

• Objective measure of habitual activity levels (via Accelerometry)

  at 20 weeks

Study Arms (2)

Control

ACTIVE COMPARATOR

1\. Usual care (control) Usual care given to patients on AAA surveillance. This includes six-monthly or annual ultrasound measurements of AAA, attendance to surveillance clinic and written (APPENDIX A) and verbal advice on managing cardiovascular risk. This advice will be based on current widely available NHS patient information15 and consists of the following information with regard to: Smoking Exercise Weight Diet

Other: Control

Community Based Exercise Programme

EXPERIMENTAL

Community based-exercise (in addition to usual care) with the choice of either: 1. Home-based exercise training Participants choosing to exercise at home will follow the programmes intended for this setting, with each exercise designed to be possible without the need for specialist equipment. 2. Gym-based exercise training Participants will exercise at their nearest Life Leisure LTD gym, following one of the instructor designed programmes , using a combination of aerobic and resistance equipment, as well as simple floor exercises. Duration and Frequency At least 50 minutes of exercise per day on three non-consecutive days of the week for 20 weeks.

Behavioral: Community based exercise programme

Interventions

Community based exercise programme BEHAVIORAL

20 week community (home or gym based) exercise programme

Community Based Exercise Programme

Control OTHER

Usual care consisting of advice.

Control

Eligibility Criteria

• Age: 60 Years - 85 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• 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

You may not qualify if:

• 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.
• 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.
• Diagnosis or treatment for a malignancy over the previous 12 months

Sponsors & Collaborators

• University of Manchester: lead
• Manchester University NHS Foundation Trust: collaborator

MeSH Terms

Conditions

Aortic Aneurysm, Abdominal

Condition Hierarchy (Ancestors)

Aortic Aneurysm; Aneurysm; Vascular Diseases; Cardiovascular Diseases; Aortic Diseases

Study Officials

• Charles McCollum, MD, FRCS

  University of Manchester

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Adam Haque, MBChB, MRCS

CONTACT

01612915848; adam.haque@manchester.ac.uk

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: OUTCOMES ASSESSOR
• Purpose: PREVENTION
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Professor

Study Record Dates

• First Submitted: December 15, 2016
• First Posted: December 20, 2016
• Study Start: November 1, 2018
• Primary Completion: January 1, 2019
• Study Completion: April 1, 2019
• Last Updated: October 17, 2018

Record last verified: 2018-10