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Effects of Aerobic Training on Exercise Capacity in Patients With Cirrhosis

Not Applicable
Completed
Conditions
Cirrhosis
Interventions
Behavioral: Aerobic exercise
Other: Usual Care
Registration Number
NCT01799785
Lead Sponsor
University of Alberta
Brief Summary

Cirrhosis is associated with a reduction in muscle mass and exercise capacity. This has an impact or morbidity and mortality. Regular aerobic exercise training is a proven effective therapy to improve exercise capacity in healthy and clinical populations. the effect of this training has not yet been evaluated in cirrhosis. The safety of this intervention also requires further study. Using a randomized controlled design, the investigators aim to conduct a pilot study evaluating the safety and efficacy of eight weeks of aerobic exercise training on aerobic capacity.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Age ≥18 and ≤70 years
  • Cirrhosis
  • Child Pugh class A or B
  • If required, primary or secondary variceal prophylaxis in place
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Exclusion Criteria
  • Post-liver transplantation
  • Hepatocellular carcinoma
  • Active non-Hepatocellular carcinoma malignancy
  • Significant cardiac disease - ejection fraction <60% or known coronary artery disease
  • Oxygen saturation at rest <95%
  • Known myopathy
  • Hemoglobin (<100 g/L)
  • Chronic renal failure on dialysis
  • Physical impairment making it impossible to ride an exercise bike or treadmill
  • Orthopedic abnormality preventing exercise training
  • HIV infection
  • Patient unwilling to consent to study
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Aerobic exerciseAerobic exerciseSupervised aerobic training 3 times per week for 8 weeks (30-60 minute sessions)
Usual care groupUsual CareThese patients will continue with their normal daily activity and will not be provided with supervised aerobic exercise training during the study period.
Primary Outcome Measures
NameTimeMethod
Change in peak exercise pulmonary oxygen uptake (peak VO2)Baseline (day 1) and Study End (8 weeks)
Secondary Outcome Measures
NameTimeMethod
Change in Quality of Life - Chronic Liver Disease QuestionnaireBaseline (day 1) and Study End (8 weeks)
Change in muscle mass as measured by thigh ultrasoundBaseline (day 1) and study end (8 weeks)

Trial Locations

Locations (1)

University of Alberta, Mazankowski Heart Institute

🇨🇦

Edmonton, Alberta, Canada

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