The Effect of Exercise Intervention on Insulin Resistance in Non-alcoholic Fatty Liver Disease (NAFLD)
NCT01834300 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60
Last updated 2024-12-18
Summary
This project examines the effects of a 4 month structured exercise intervention program in patients with non-alcoholic fatty liver disease (NAFLD). We will examine changes in total and depot-specific (i.e.in different tissues, liver, muscle and pancreas)fat. We will correlate these with measurements of the insulin from the liver. The hypothesis is that by reducing fat in these specific depots we can reduce insulin resistance and prevent progression to diabetes.
Conditions
- Non Alcoholic Fatty Liver Disease
Interventions
- BEHAVIORAL
-
Unsupervised exercise training
The patients will be given lecture on lifestyle changes and its benefitial effects on health at the begining of the study by the exercise trainer. There will be no conatct with the exercise trainer for the period of intervention for 4 months.
- BEHAVIORAL
-
Supervised exercise training
Patients will be encouraged to exercise four times per week for 30-45 min at 60-80 % of maximal heart rate, with a 5 min warm-up and warm-down. Participants will be given free access to a variety of affiliated sports centres and will use the Wellness Key system, a software program that enables researchers to remotely track the exercise activity of participants very accurately. To ensure compliance with rest or exercise, all participants of both groups will have their mean physical activity level in 2 non-consecutive weeks evaluated with an ambulatory accelerometer.
Sponsors & Collaborators
-
Royal Liverpool University Hospital
collaborator OTHER_GOV -
University of Surrey
collaborator OTHER -
Imperial College London
collaborator OTHER -
Royal Surrey County Hospital NHS Foundation Trust
collaborator OTHER -
University of Liverpool
lead OTHER
Principal Investigators
-
Daniel Cuthbertson, BSc PhD MRCP · University of Liverpool
-
Fariba Shojaee-Moradie, BSc PhD · University of Surrey
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 20 Years
- Max Age
- 65 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2009-01-01
- Primary Completion
- 2013-04-01
- Completion
- 2013-04-01
Countries
- United Kingdom
Study Locations
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